<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2 20190208//EN" "http://jats.nlm.nih.gov/publishing/1.2/JATS-journalpublishing1.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="systematic-review" dtd-version="1.2" xml:lang="en">
    <front>
        <journal-meta>
            <journal-id journal-id-type="pmc">F1000Research</journal-id>
            <journal-title-group>
                <journal-title>F1000Research</journal-title>
            </journal-title-group>
            <issn pub-type="epub">2046-1402</issn>
            <publisher>
                <publisher-name>F1000 Research Limited</publisher-name>
                <publisher-loc>London, UK</publisher-loc>
            </publisher>
        </journal-meta>
        <article-meta>
            <article-id pub-id-type="doi">10.12688/f1000research.183567.1</article-id>
            <article-categories>
                <subj-group subj-group-type="heading">
                    <subject>Systematic Review</subject>
                </subj-group>
                <subj-group>
                    <subject>Articles</subject>
                </subj-group>
            </article-categories>
            <title-group>
                <article-title>Male Sterility Systems in Hybrid Rice Development for Abiotic Stress Tolerance: A Systematic Review of Genetic Sources, Molecular Mechanisms, and Breeding Strategies</article-title>
                <fn-group content-type="pub-status">
                    <fn>
                        <p>[version 1; peer review: awaiting peer review]</p>
                    </fn>
                </fn-group>
            </title-group>
            <contrib-group>
                <contrib contrib-type="author" corresp="yes">
                    <name>
                        <surname>Mustaina</surname>
                        <given-names>Nur</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Data Curation</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Original Draft Preparation</role>
                    <role content-type="http://credit.niso.org/">Writing &#x2013; Review &amp; Editing</role>
                    <uri content-type="orcid">https://orcid.org/0009-0005-4744-560X</uri>
                    <xref ref-type="corresp" rid="c1">a</xref>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Kabosu</surname>
                        <given-names>Yohana Ista</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Data Curation</role>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <role content-type="http://credit.niso.org/">Project Administration</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Nisa</surname>
                        <given-names>Muthi'ah Khairun</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Data Curation</role>
                    <role content-type="http://credit.niso.org/">Formal Analysis</role>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Marbun</surname>
                        <given-names>Arifin</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Funding Acquisition</role>
                    <role content-type="http://credit.niso.org/">Investigation</role>
                    <role content-type="http://credit.niso.org/">Project Administration</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Cahyadi</surname>
                        <given-names>Dwi</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Software</role>
                    <role content-type="http://credit.niso.org/">Supervision</role>
                    <role content-type="http://credit.niso.org/">Validation</role>
                    <uri content-type="orcid">https://orcid.org/0009-0009-8299-489X</uri>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Sitanggang</surname>
                        <given-names>Romauli Therecia</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Funding Acquisition</role>
                    <role content-type="http://credit.niso.org/">Project Administration</role>
                    <role content-type="http://credit.niso.org/">Visualization</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Badar</surname>
                        <given-names>Feliksia Silvana Pau</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Formal Analysis</role>
                    <role content-type="http://credit.niso.org/">Software</role>
                    <role content-type="http://credit.niso.org/">Supervision</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Anisiyah</surname>
                        <given-names>Anisiyah</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Formal Analysis</role>
                    <role content-type="http://credit.niso.org/">Investigation</role>
                    <role content-type="http://credit.niso.org/">Methodology</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <contrib contrib-type="author" corresp="no">
                    <name>
                        <surname>Sari</surname>
                        <given-names>Milga</given-names>
                    </name>
                    <role content-type="http://credit.niso.org/">Data Curation</role>
                    <role content-type="http://credit.niso.org/">Validation</role>
                    <role content-type="http://credit.niso.org/">Visualization</role>
                    <xref ref-type="aff" rid="a1">1</xref>
                </contrib>
                <aff id="a1">
                    <label>1</label>Department of Agronomy and Horticulture, Faculty of Agriculture, IPB University, Bogor, 16680, Indonesia</aff>
            </contrib-group>
            <author-notes>
                <corresp id="c1">
                    <label>a</label>
                    <email xlink:href="mailto:nurmustaina7@gmail.com">nurmustaina7@gmail.com</email>
                </corresp>
                <fn fn-type="conflict">
                    <p>No competing interests were disclosed.</p>
                </fn>
            </author-notes>
            <pub-date pub-type="epub">
                <day>18</day>
                <month>6</month>
                <year>2026</year>
            </pub-date>
            <pub-date pub-type="collection">
                <year>2026</year>
            </pub-date>
            <volume>15</volume>
            <elocation-id>968</elocation-id>
            <history>
                <date date-type="accepted">
                    <day>8</day>
                    <month>6</month>
                    <year>2026</year>
                </date>
            </history>
            <permissions>
                <copyright-statement>Copyright: &#x00a9; 2026 Mustaina N et al.</copyright-statement>
                <copyright-year>2026</copyright-year>
                <license xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
                </license>
            </permissions>
            <self-uri content-type="pdf" xlink:href="https://f1000research.com/articles/15-968/pdf"/>
            <abstract>
                <sec>
                    <title>Research Background</title>
                    <p>Climate change-induced abiotic stresses, alongside rising global food demand, have increased the urgency to develop hybrid rice cultivars with greater productivity, yield stability, and environmental adaptability. Male sterility-based breeding systems play a pivotal role in hybrid rice improvement, while recent advances in molecular technologies have accelerated the incorporation of stress-tolerant traits. This study, therefore, aims to systematically evaluate hybrid rice breeding strategies based on male-sterility systems for abiotic stress tolerance and to identify emerging trends, technological advances, and remaining research gaps.</p>
                </sec>
                <sec>
                    <title>Methods</title>
                    <p>A systematic literature review (SLR) was conducted on studies published between 2017 and 2026. Using the PRISMA framework and PICO-based eligibility criteria, 33 articles were selected for analysis. Descriptive and thematic synthesis methods were applied to assess developments in male sterility systems, molecular breeding approaches, stress-response mechanisms, and experimental designs used in hybrid rice research.</p>
                </sec>
                <sec>
                    <title>Results</title>
                    <p>The findings show that the three-line system based on cytoplasmic male sterility (CMS) remains the most widely adopted breeding platform because of its reproductive stability, efficient fertility restoration, and extensive commercial use. Advances in molecular breeding&#x2014;including QTL introgression, marker-assisted backcrossing, genomic selection, and CRISPR/Cas9 genome editing&#x2014;have strengthened the development of stress-resilient hybrids by targeting ion homeostasis, osmotic regulation, antioxidative defense, and root architecture. Nevertheless, important limitations remain. Most studies examine only single-stress environments, despite the growing occurrence of multiple and sequential abiotic stresses associated with climate change. Moreover, the dominance of controlled-environment experiments restricts the broader applicability of findings under heterogeneous field conditions, where genotype&#x2013;environment interactions strongly affect hybrid performance. These findings underscore the need for integrated breeding frameworks combining multi-trait pyramiding, multilocation field evaluation, and the integration of multi-omics technologies with physiological characterization to accelerate the development of climate-resilient hybrid rice cultivars.</p>
                </sec>
            </abstract>
            <kwd-group kwd-group-type="author">
                <kwd>Abiotic Stress; CRISPR/Cas9; Cytoplasmic Male Sterility; Hybrid Rice; Molecular Breeding.</kwd>
            </kwd-group>
            <funding-group>
                <award-group id="fund-1">
                    <funding-source>The lead author gratefully acknowledges the financial support provided by the Indonesia Endowment Fund for Education (Lembaga Pengelola Dana Pendidikan/LPDP) for the master&#x2019;s research on which this article is based</funding-source>
                </award-group>
                <funding-statement>This research was funded by the Indonesia Endowment Fund for Education (Lembaga Pengelola Dana Pendidikan/LPDP), Ministry of Finance of the Republic of Indonesia.</funding-statement>
                <funding-statement>
                    <italic>The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.</italic>
                </funding-statement>
            </funding-group>
        </article-meta>
    </front>
    <body>
        <sec id="sec4" sec-type="intro">
            <title>1. Introduction</title>
            <p>Increasing global food demand, climate change, and land resource degradation have made improving crop productivity and resilience to abiotic stress a major challenge in rice development. As the staple food for more than half of the world&#x2019;s population, rice production plays a strategic role in maintaining global food security. The 
                <xref ref-type="bibr" rid="ref13">FAO (2025)</xref> projects that global rice consumption will increase by approximately 1% annually until 2034, with Asia accounting for nearly 69% of total consumption growth. At the same time, the increasing frequency of drought, salinity, extreme temperatures, and flooding associated with climate change continues to constrain rice productivity across major production regions (
                <xref ref-type="bibr" rid="ref5">Aruneshwaran et al., 2025</xref>). These conditions highlight the urgent need for breeding innovations that enhance yield performance while strengthening crop adaptability under increasingly unstable environmental conditions.</p>
            <p>Hybrid rice has emerged as one of the most promising breeding approaches for addressing these challenges. By exploiting heterosis, hybrid rice has been reported to achieve a 15&#x2013;20% yield advantage over elite inbred cultivars (
                <xref ref-type="bibr" rid="ref41">Virmani &amp; Kumar, 2004</xref>). Commercial hybrid rice production is generally based on two major systems, namely the three-line and two-line systems. The three-line system, which relies on cytoplasmic male sterility (CMS), uses a cytoplasmic male-sterile line (A line), a maintainer line (B line), and a fertility restorer line (R line) to produce stable, genetically uniform hybrid seeds. In contrast, the two-line system utilizes genic male-sterile lines whose sterility is regulated by temperature and photoperiod, thereby simplifying hybrid seed production by eliminating the need for a maintainer line (
                <xref ref-type="bibr" rid="ref16">Guo-hui &amp; Long-ping, 2015</xref>). This system includes thermo-sensitive genic male sterility (TGMS), photoperiod-sensitive genic male sterility (PGMS), and photoperiod-thermo-sensitive genic male sterility (PTGMS) (
                <xref ref-type="bibr" rid="ref46">Xu et al., 2023</xref>). The stability of male sterility expression in the female parent line is a critical determinant of successful hybrid seed production, as it prevents self-pollination and maintains the genetic purity of hybrid seeds.</p>
            <p>Global climate change has further increased the complexity of hybrid rice development by intensifying abiotic stresses that affect plant growth, reproductive stability, and grain yield. 
                <xref ref-type="bibr" rid="ref19">Kandpal et al. (2020)</xref> demonstrated that hormonal regulation associated with abiotic stress responses influences peduncle elongation, spikelet fertility, and grain filling in male sterile lines. These findings suggest that the success of hybrid rice systems depends not only on heterotic yield potential but also on sterile lines&#x2019; ability to maintain reproductive stability under environmental stress. In recent years, advances in molecular breeding technologies, including marker-assisted breeding, QTL introgression, genomic selection, and CRISPR/Cas9 genome editing, have accelerated the incorporation of stress-tolerant traits into hybrid rice breeding programs (
                <xref ref-type="bibr" rid="ref15">Gregorio et al., 2013</xref>). Nevertheless, information on the relationships among male sterility systems, hybrid performance, and physiological and molecular mechanisms of adaptation to abiotic stress remains fragmented across the literature and has not yet been comprehensively synthesized.</p>
            <p>Furthermore, most existing studies focus on single-stress conditions in controlled environments, whereas combinations of stresses, such as drought, heat, and salinity, are increasingly common in modern agroecosystems (
                <xref ref-type="bibr" rid="ref39">Suzuki et al., 2014</xref>; 
                <xref ref-type="bibr" rid="ref2">Altaf et al., 2021</xref>; 
                <xref ref-type="bibr" rid="ref4">Anwar et al., 2021</xref>). Limited multilocation evaluations and insufficient integration of multi-omics approaches have also restricted the understanding of hybrid adaptation stability under heterogeneous field conditions. Therefore, a systematic literature review is required to synthesize current research developments, identify emerging trends and knowledge gaps, and formulate future directions for the development of abiotic-stress-tolerant hybrid rice that is more adaptive and sustainable.</p>
            <p>Based on this background, the present study aims to comprehensively analyze the role of male sterility systems in the development of abiotic stress-tolerant hybrid rice using a systematic literature review. The findings are expected to provide a scientific foundation for advancing breeding strategies and integrating modern molecular technologies to develop hybrid rice cultivars with improved productivity, stability, and resilience under global climate change.</p>
        </sec>
        <sec id="sec5">
            <title>2. Material and methods</title>
            <p>This study employed a systematic literature review (SLR) to synthesise scientific evidence on the development of hybrid rice using male-sterility systems for abiotic stress tolerance. The review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to ensure methodological transparency and reproducibility (
                <xref ref-type="bibr" rid="ref10">Donthu et al., 2021</xref>; 
                <xref ref-type="bibr" rid="ref34">Permatasari et al., 2025</xref>). The review process consisted of four stages: study identification, duplicate removal, title and abstract screening, and full-text eligibility assessment based on predefined inclusion and exclusion criteria.</p>
            <p>A comprehensive literature search was conducted using the Scopus and PubMed databases because of their broad coverage of peer-reviewed publications in agricultural, biological, molecular, and environmental sciences. The search strategy combined controlled keywords and Boolean operators related to male sterility systems, hybrid rice, and abiotic stress. The following search syntax was applied across both databases: ((&#x201c;male sterile&#x201d; OR &#x201c;cytoplasmic male sterility*&#x201d; OR &#x201c;genic male sterile*&#x201d; OR &#x201c;restorer&#x201d; OR &#x201c;maintainer&#x201d;) AND (&#x201c;rice&#x201d; OR &#x201c;Oryza sativa&#x201d; OR &#x201c;paddy&#x201d; OR &#x201c;hybrid rice&#x201d;) AND (&#x201c;abiotic stress&#x201d; OR &#x201c;environmental stress&#x201d; OR &#x201c;heat stress&#x201d; OR &#x201c;salinity stress&#x201d; OR &#x201c;drought stress&#x201d; OR &#x201c;salt stress&#x201d; OR &#x201c;water stress&#x201d;))*.</p>
            <p>The initial search retrieved 103 records. Additional filters were applied to include only English-language articles published between 2017 and 2026. In Scopus, the search was further restricted to the subject areas of Agricultural and Biological Sciences, Biochemistry, Genetics and Molecular Biology, and Environmental Sciences, and to original research articles published in peer-reviewed journals. After filtering, 56 articles met the preliminary eligibility criteria, comprising 49 records from Scopus and 7 from PubMed.</p>
            <p>All records were consolidated into a single database, and seven duplicate articles were removed, leaving 49 studies for screening. Title and abstract screening was conducted independently by five reviewers (NM, AM, MKN, DC, and RS). Studies unrelated to hybrid rice, male sterility systems, or abiotic stress responses were excluded. Following screening, 39 studies proceeded to full-text assessment. All full-text articles were successfully retrieved and evaluated for conceptual relevance and methodological suitability. The final selection process followed the PRISMA framework, and the overall workflow is presented in 
                <xref ref-type="fig" rid="f1">
Figure 1</xref>.</p>
            <fig fig-type="figure" id="f1" orientation="portrait" position="float">
                <label>Fig 1. </label>
                <caption>
                    <title>PRISMA 2020 flow diagram for the selection of studies on male sterility-based hybrid rice under abiotic stress.</title>
                </caption>
                <graphic id="gr1" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/202622/c3506595-9b10-4013-b9f6-1fddb53034e4_figure1.gif"/>
            </fig>
            <p>An eligibility assessment was conducted on 39 full-text articles to identify studies related to the development of abiotic stress-tolerant hybrid rice using male sterility systems. Study selection followed the PICO framework (Population, Intervention, Comparison, Outcome) proposed by 
                <xref ref-type="bibr" rid="ref12">Eldawlatly et al. (2018)</xref> with predefined inclusion and exclusion criteria summarised in 
                <xref ref-type="table" rid="T1">
Table 1</xref>. Articles were evaluated systematically based on their titles, abstracts, and full texts to ensure relevance to the objectives of the review.</p>
            <table-wrap id="T1" orientation="portrait" position="float">
                <label>
Table 1. </label>
                <caption>
                    <title>Eligibility criteria based on the PICO framework.</title>
                </caption>
                <table content-type="article-table" frame="hsides">
                    <thead>
                        <tr>
                            <th align="left" colspan="1" rowspan="1" valign="top">
Component</th>
                            <th align="left" colspan="1" rowspan="1" valign="top">Criteria</th>
                        </tr>
                    </thead>
                    <tbody>
                        <tr>
                            <td align="left" colspan="1" rowspan="1" valign="top">
                                <bold>Population (P)</bold>
</td>
                            <td align="left" colspan="1" rowspan="1" valign="top">Studies conducted on rice (Oryza sativa L.)</td>
                        </tr>
                        <tr>
                            <td align="left" colspan="1" rowspan="1" valign="top">
                                <bold>Intervention (I)</bold>
</td>
                            <td align="left" colspan="1" rowspan="1" valign="top">Studies involving male sterility systems under abiotic stress conditions</td>
                        </tr>
                        <tr>
                            <td align="left" colspan="1" rowspan="1" valign="top">
                                <bold>Comparison (C)</bold>
</td>
                            <td align="left" colspan="1" rowspan="1" valign="top">Comparisons between stressed and non-stressed conditions and among evaluated genetic materials</td>
                        </tr>
                        <tr>
                            <td align="left" colspan="1" rowspan="1" valign="top">
                                <bold>Outcome (O)</bold>
</td>
                            <td align="left" colspan="1" rowspan="1" valign="top">Improvement in abiotic stress tolerance, fertility restoration, agronomic traits, and hybrid yield performance under stress conditions</td>
                        </tr>
                    </tbody>
                </table>
            </table-wrap>
            <p>Six studies were excluded because they involved non-rice commodities (
                <xref ref-type="bibr" rid="ref51">Zhao et al., 2022</xref>), hybrid approaches unrelated to male sterility systems (
                <xref ref-type="bibr" rid="ref35">Prasanth et al., 2017</xref>; 
                <xref ref-type="bibr" rid="ref27">Mo et al., 2023</xref>; 
                <xref ref-type="bibr" rid="ref21">Li et al., 2025</xref>), or focused solely on stress-response mechanisms without evaluating abiotic stress treatments in hybrid rice systems (
                <xref ref-type="bibr" rid="ref45">Xia &amp; Luo, 2023</xref>; 
                <xref ref-type="bibr" rid="ref19">Kandpal et al., 2020</xref>). Consequently, 33 articles were included in the final analysis. Data extraction was conducted systematically using a structured spreadsheet database. Extracted information included study characteristics, male sterility systems, genetic backgrounds, abiotic stress treatments, physiological and molecular responses, agronomic performance, and breeding strategies.</p>
            <p>Due to substantial variation in experimental design, stress intensity, and evaluation parameters, data were synthesised using a narrative-qualitative approach rather than quantitative meta-analysis. The studies were grouped by abiotic stress type: drought, salinity, heat, low temperature, phosphorus deficiency, and combined stresses. Analyses focused on the effectiveness of male sterility systems and hybrid breeding strategies in improving stress tolerance, reproductive stability, and agronomic performance. The synthesis results are presented through summary tables, conceptual figures, and analytical narratives to identify current research trends and critical gaps in climate-resilient hybrid rice breeding.</p>
        </sec>
        <sec id="sec6" sec-type="results">
            <title>3. Result</title>
            <sec id="sec7">
                <title>3.1 Keyword Co-occurrence and temporal research trends</title>
                <p>All literature included in this review met the eligibility criteria presented in 
                    <xref ref-type="table" rid="T1">
Table 1</xref> and comprised studies published between 2017 and 2026 on environmental stress tolerance in hybrid rice. Bibliometric visualisation using VOSviewer identified two major thematic clusters (
                    <xref ref-type="fig" rid="f2">
Figure 2</xref>): drought-related studies associated with CRISPR/Cas9, agronomic traits, and homozygosity, and more recent heat-stress research linked to metabolic regulation, catalase activity, and hydrogen peroxide scavenging. Node size indicated keyword frequency, with genetics, phenotype, drought stress, and gene ontology emerging as the most dominant themes. At the same time, network density highlighted strong co-occurrence among genetics, phenotype, environmental stress, and genetic engineering. Temporal overlay analysis further revealed a shift in research focus from foundational topics such as hybridisation, QTL mapping, genomics, and combining ability (2018) toward drought tolerance, CRISPR/Cas9, and heat stress (2020), followed by recent emphasis (2022&#x2013;2026) on Rf3 genetics, gene expression, enzymology, antioxidant regulation, and high-temperature tolerance. Overall, these trends indicate a shift from conventional breeding toward molecular and physiological strategies to improve antioxidant defence systems and heat resilience in hybrid rice.</p>
                <fig fig-type="figure" id="f2" orientation="portrait" position="float">
                    <label>Fig 2. </label>
                    <caption>
                        <title>Distribution of articles by abiotic stress.</title>
                    </caption>
                    <graphic id="gr2" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/202622/c3506595-9b10-4013-b9f6-1fddb53034e4_figure2.gif"/>
                </fig>
            </sec>
            <sec id="sec8">
                <title>3.2 Diversity and functional architecture of male sterility systems in hybrid rice breeding</title>
                <p>Hybrid rice (Oryza sativa) performance is strongly influenced by Cytoplasmic Male Sterility (CMS) systems, particularly Wild-Abortive CMS (WA-CMS), which are regulated by mitochondrial genes that disrupt pollen development and enable efficient hybrid seed production. Beyond reproductive control, CMS systems contribute to agronomic improvement through enhanced specific combining ability (SCA), heterosis, and hybrid vigor arising from interactions among CMS, maintainer, and restorer lines. CMS-derived hybrids also exhibit superior germination, stronger root architecture, and improved seedling establishment under drought stress, reflecting the importance of nuclear&#x2013;cytoplasmic interactions and stress-responsive metabolic regulation.</p>
                <p>As summarized in 
                    <xref ref-type="table" rid="T2">
Table 2</xref>, hybrid rice breeding over the last decade has been predominantly centred on CMS-based three-line systems, with WA-CMS remaining the most widely utilized platform because of its stable sterility expression, broad fertility restoration capacity, and strong association with high yield performance (
                    <xref ref-type="bibr" rid="ref18">Hong-Bing et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref44">Widyastuti et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref22">Liao et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref25">Luo et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref11">El-mowafi et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref26">Madhusudan et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref6">Awad-allah et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref20">Li et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref14">Ghazy et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref7">Bhuyan et al., 2025</xref>). The recurrent use of elite CMS lines such as IR58025A and IR69625A further indicates the continued dependence of breeding programs on a limited number of reliable cytoplasmic donor sources. At the molecular level, CMS is associated with aberrant mitochondrial genes that induce maternally inherited male sterility, providing an efficient biological system for large-scale hybrid seed production without manual emasculation.</p>
                <table-wrap id="T2" orientation="portrait" position="float">
                    <label>
Table 2. </label>
                    <caption>
                        <title>Components, genetic aspects, and performance of male sterility-based hybrid rice (Oryza sativa).</title>
                    </caption>
                    <table content-type="article-table" frame="hsides">
                        <thead>
                            <tr>
                                <th align="left" colspan="1" rowspan="1" valign="top">Material</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">Lines</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">System component</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">Functional role in hybrid system</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">Key findings</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">Genetic aspect</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">References</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">Main findings related to hybrid performance</th>
                                <th align="left" colspan="1" rowspan="1" valign="top">Stress type</th>
                            </tr>
                        </thead>
                        <tbody>
                            <tr>
                                <td align="left" colspan="1" rowspan="3" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A line:</bold> IR58025A, APMS6A</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">WA-CMS
</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">
                                    <xref ref-type="bibr" rid="ref36">Priyadarshi et al. (2025)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Hybrids carrying Rf3/Rf4 showed higher fertility restoration, high SCA, and significant heterosis for grain yield</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Cold</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> KMR 3; IR 93376- B- B- 130; IR 96322&#x2013;34-223- B- 1-1- 1; IR 102774&#x2013;31- 21- 2- 4-7; TDK 1; IR 99734:1&#x2013;33- 69- 1- 12- LSM- 1; IR 99734:1&#x2013;33- 69- 1- 9- LSM- 1; IR 99734:1&#x2013;33- 69- 1- 39-6; IR 99734:1&#x2013;33&#x2013;69-1- 12-4; IR 102783:2&#x2013;70-91- 2- 1-2 and IR83383- B- B (RP5333-12&#x2013;2-1); KMR3</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>M-line
</bold>: R 58025B</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> IR58025A; IR80154A; IR80156A; GMJ13A; GMJ14A; GMJ15A</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref44">Widyastuti et al. (2017)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Certain hybrids maintained better germination and root vigor under drought stress</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Drought &amp; Waterlogging</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> PK90; R3; PK12; R32; BP11</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L. subsp. indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> R225</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Effective restoration of pollen fertility in CMS hybrids</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear restorer gene (Rf gene)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref42">Wang et al. (2025)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">WT plants maintained higher yield stability than ts12 mutants under high temperature</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Chenghui727</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Effective restoration of pollen fertility in CMS hybrids</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear restorer gene (Rf gene)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref30">Nabi et al. (2022)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Hybrid Deyou4727 showed superior yield and root performance under drought</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> 996 (HT 996); 343 (HS 343)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Effective restoration of pollen fertility in CMS hybrids</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear restorer gene (Rf gene)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref48">You et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Mixed nitrogen improved spikelet fertility and yield under heat stress</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> Gang46A (L1); IR69625A (L2)</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref6">Awad-allah et al. (2022)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Several hybrids exhibited positive SCA and lower yield reduction under drought</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> NRL 2; NRL 9; NRL 10; NRL 11; NRL 12; NRL 29; NRL 42; NRL 43; NRL 44; NRL 47; NRL 50; Giza178</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Wan2304S; S240; 2X5S; H03S; N95076S; N5088S.(etc)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">ESGMS</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Environment-dependent male sterility for two-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Conditional male sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear-controlled sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref50">Zhang et al. (2021)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">CMS and restorer lines showed high genetic purity suitable for hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">O. sativa ssp japonica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> oshsp60-3b male-sterile mutant</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">ESGMS</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Environment-dependent male sterility for two-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Conditional male sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear-controlled sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref23">Lin et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">High temperature caused pollen sterility and reproductive abnormalities</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L. ssp japonica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> Chinsurah Boro II</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">BT-CMS
</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Female parent in three-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Reliable cytoplasmic male sterility with effective fertility restoration by Rf genes</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Cytoplasmic&#x2013;nuclear interaction involving mitochondrial sterility genes</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref49">Zhang et al. (2017)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Fertility restoration was strongly associated with restorer gene combinations</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L. subsp. indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> R996, R4628</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Conditional male sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear-controlled sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref52">Zhou et al. (2025)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat stress reduced reproductive performance and grain filling efficiency</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L. subsp. japonica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line
</bold>: Shen 21A</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">BT-CMS
</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Reliable cytoplasmic male sterility with effective fertility restoration by Rf genes</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Cytoplasmic&#x2013;nuclear interaction involving mitochondrial sterility genes</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref32">Niu et al. (2025)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat stress disrupted reproductive tissue development</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Salinity</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> KMR-3R; IL-1; IL-2; IL-3; IL-4; IL-5; IL-6; IL-7; IL-8</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Conditional male sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear-controlled sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref31">Nagaraju et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Non-additive gene action contributed strongly to hybrid superiority</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza rufipogon Griff., Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> R974</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Conditional male sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear-controlled sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref9">Ding et al. (2022)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat stress disrupted reproductive tissue development</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> Peiai 64S; Shen 08S</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">PTGMS</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Environment-sensitive male sterility for two-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Stable sterility&#x2013;fertility transition under specific temperature and photoperiod conditions</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Photo-thermo sensitive nuclear sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref8">Chen et al. (2021)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Hybrid lines produced higher biomass and yield than parental lines</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa L. subsp. indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> APMS-6A</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">WA-CMS
</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref38">Sravanraju et al. (2024)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Several crosses showed positive heterosis and superior yield</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> RPHR-1005R, RPHR6339-4-16-14-2 (IL1); RPHR6339-4-16-14-3 (IL2); RPHR6339-4-16-14&#x2013;7 (IL3); RPHR6339-4-16-14-8 (IL4); RPHR6339-4-16-14-16 (IL5); RPHR6339-4-16-14-22 (IL6)</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa L. subsp. Indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>M-line:</bold> 733Srr22-T1447&#x2013;1</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">GMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref37">Sheng et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Heat stress reduced pollen viability and seed setting</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> HZrr22-T1349&#x2013;3</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Huhan 74S</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">PTGMS</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Environment-sensitive male sterility for two-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Stable sterility&#x2013;fertility transition under specific temperature and photoperiod conditions</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Photo-thermo sensitive nuclear sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref24">Liu et al. (2021)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Hybrids showed stronger stress-defense responses</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L. subsp. Nipponbare, Indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> ospks2&#x2013;1, ospks2&#x2013;2, ospks2&#x2013;3</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">MS-
                                    <italic toggle="yes">mutant</italic>
</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref53">Zou et al. (2018)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Hybrid rice maintained more stable productivity across environments</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L.</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>M-line:</bold> APMS6B</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref26">Madhusudan et al. (2022)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">High SCA values supported hybrid yield advantages</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Drought &amp; Salinity</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Peiai 64S, Y58S</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">PTGMS</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Environment-sensitive male sterility for two-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Stable sterility&#x2013;fertility transition under specific temperature and photoperiod conditions</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Photo-thermo sensitive nuclear sterility gene</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref47">Yang &amp; Zhang (2020)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Stress reduced grain filling, but hybrids maintained better productivity</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Padi (Oryza sativa L.).</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Guihui5501</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Effective restoration of pollen fertility in three-line hybrids</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear restorer gene (Rf gene)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref43">Wei et al. (2024)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat stress significantly affected spikelet fertility</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> M.J.5460S, Giza177, Sakha105, Sakha106, GZ7768</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">rTGMS (reverse thermo-responsive genic male sterile)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Temperature-dependent male sterility for two-line hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Reversible fertility alteration regulated by temperature changes</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear gene-mediated reverse thermo-sensitive male sterility</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref1">Abdelrahman et al. (2021)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Hybrids activated stress-responsive pathways under abiotic stress</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> IR58025A</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref11">El-mowafi et al. (2021)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Hybrid combinations showed superior agronomic performance</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> PR2, IR25571-31R, Giza-Basmati-201, PR1</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa L.</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> CRMS31A, CRMS32A</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref7">Bhuyan et al. (2025)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stress-tolerant hybrids maintained relatively stable productivity</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> IR 42266&#x2013;29-3R</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> Jiabuyu</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">DMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Facilitation of hybrid breeding through dominant male sterility</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Dominant inheritance of male sterility</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Dominant nuclear sterility gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref33">Pang et al. (2017)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS-associated genes affected pollen fertility</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line: 3</bold>3, 84, 611, 9311, CDR22, Ce253, Cheng-Hui177, Duo-Xi 1 Hao, Fu838, Guang-Hui998, Gui99, Hang 1 Hao, Lu-Hui17, Mian-Hui725, Ming-Hui63, Ming-Hui86, Min-Hui3301, Mi-Yang46, R9308, Shu-Hui527, Wan-Hui057, Yan-Hui559, Yi-Hui1577, Zhe-Hui7954, Zhong-Hui8006</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> wsl3 mutant</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref18">Hong-Bing et al. (2017)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Disruption in reproductive processes contributed to sterility</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Zhenhui 714 (R714)</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> IR69625A (Wild abortive (WA) CMSline; G46A (Gambiaca CMS line)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">WA-CMS;</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction for three-line hybrid breeding; Gambiaca Cytoplasmic male sterility for hybrid breeding</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Effective sterility expression in hybrid rice system</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial sterility-associated gene with nuclear&#x2013;cytoplasmic interaction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref17">Hamad et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Hybrid genotypes performed better under stress environments</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Heat</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Giza 178R</td>
                                <td colspan="1" rowspan="1"/>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> Zhonghui9308</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Effective restoration of pollen fertility in CMS hybrids</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Nuclear restorer gene (Rf gene)</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref3">Anis et al. (2018)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Some hybrids showed broad adaptation across environments</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">P Deficiency</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>M-line:</bold> XieqingzaoB</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> 36A; 52A</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref22">Liao et al. (2019)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS-related pathways affected fertility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">P Deficiency</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> GXU16, GXU20, GXU28 (WT); GXU16&#x2013;19, GXU20&#x2013;8, GXU28&#x2013;12</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="2" valign="top">Oryza sativa L. subsp. indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> II-32A</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">
                                    <xref ref-type="bibr" rid="ref25">Luo et al. (2019)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Fertility abnormalities were linked to disrupted pollen formation</td>
                                <td align="left" colspan="1" rowspan="2" valign="top">Salinity</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> F6; BIL627</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="3" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> IR69625A; G46</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">
                                    <xref ref-type="bibr" rid="ref14">Ghazy et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Certain hybrids maintained yield under limited water conditions</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Salinity</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> R146; R727; RH103; R8258; HZ; R938; R4923; R1391</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>M-line:</bold> Dexiang074B (074B)</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="3" valign="top">Oryza sativa</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>A-line:</bold> Dexiang074A</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">CMS</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Male sterility induction</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Stable sterility expression</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Mitochondrial gene</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">
                                    <xref ref-type="bibr" rid="ref20">Li et al. (2023)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Oxidative stress influenced reproductive stability</td>
                                <td align="left" colspan="1" rowspan="3" valign="top">Salinity</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>R-line:</bold> R146; R727; RH103; R8258; HZ, R938; R4923; R1391</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <bold>M-line:</bold> Dexiang074B (074B)</td>
                            </tr>
                            <tr>
                                <td align="left" colspan="1" rowspan="1" valign="top">Oryza sativa L. subsp. indica</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">R-line: KMR3; IL50&#x2013;13</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Restorer</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Pollen fertility restoration</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Effective restoration of pollen fertility in CMS hybrids</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Nuclear restorer gene (Rf gene)</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">
                                    <xref ref-type="bibr" rid="ref40">Thummala et al. (2022)</xref>
                                </td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Hybrid combinations expressed significant heterosis for yield-related traits</td>
                                <td align="left" colspan="1" rowspan="1" valign="top">Salinity</td>
                            </tr>
                        </tbody>
                    </table>
                </table-wrap>
                <p>Despite these advantages, several constraints continue to limit the long-term sustainability of CMS-based breeding. Narrow cytoplasmic diversity increases vulnerability to environmental and biological stresses, while sterility expression in certain CMS backgrounds remains sensitive to temperature and photoperiod fluctuations (
                    <xref ref-type="bibr" rid="ref24">Liu et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref50">Zhang et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref23">Lin et al., 2023</xref>). Another major challenge is the requirement for compatible nuclear restorer-of-fertility (Rf
) genes to achieve complete fertility recovery (
                    <xref ref-type="bibr" rid="ref30">Nabi et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref48">You et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>; 
                    <xref ref-type="bibr" rid="ref42">Wang et al., 2025</xref>). Consequently, recent research has increasingly shifted toward improving the efficiency of fertility restoration, diversifying restorer germplasm, and elucidating the genomic regulation of nucleus&#x2013;cytoplasm interactions (
                    <xref ref-type="bibr" rid="ref3">Anis et al., 2018</xref>; 
                    <xref ref-type="bibr" rid="ref17">Hamad et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref31">Nagaraju et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>; 
                    <xref ref-type="bibr" rid="ref42">Wang et al., 2025</xref>; 
                    <xref ref-type="bibr" rid="ref32">Niu et al., 2025</xref>).</p>
                <p>The strategic importance of restorer lines is evident from the repeated use of elite genotypes such as KMR, Guihui5501, Chenghui727, and Zhonghui9308, which exhibit stable fertility restoration and superior performance across multiple CMS backgrounds. However, the repeated deployment of these lines also indicates that current breeding programs still rely on a relatively narrow pool of elite donor germplasm. At the genetic level, fertility restoration is primarily regulated by nuclear-encoded Rf genes that suppress sterility-associated mitochondrial transcripts, representing a clear example of coordinated nucleus&#x2013;cytoplasm coevolution in crop breeding systems (
                    <xref ref-type="bibr" rid="ref3">Anis et al., 2018</xref>; 
                    <xref ref-type="bibr" rid="ref30">Nabi et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref31">Nagaraju et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>; 
                    <xref ref-type="bibr" rid="ref42">Wang et al., 2025</xref>).</p>
                <p>To improve breeding efficiency, recent programs increasingly integrate molecular markers, high-throughput genotyping, and genomic selection to rapidly identify and develop superior restorer lines. These advances reflect the broader transition from conventional phenotype-based selection toward genomics-assisted hybrid breeding to enhance stress resilience, fertility stability, and sustainable yield performance under changing environmental conditions.</p>
            </sec>
            <sec id="sec9">
                <title>3.3. Physiological and molecular mechanisms of stress tolerance in hybrid Rice</title>
                <p>CMS-based hybrid rice exhibits integrated physiological and molecular adaptations that enhance tolerance to major abiotic stresses, including drought, heat, salinity, nutrient deficiency, and low temperature (
                    <xref ref-type="fig" rid="f3">
Figure 3</xref>). Physiological responses mainly involve improved water-use efficiency, carbohydrate regulation, and antioxidant defense systems (
                    <xref ref-type="bibr" rid="ref53">Zou et al., 2018</xref>; 
                    <xref ref-type="bibr" rid="ref22">Liao et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref47">Yang &amp; Zhang, 2020</xref>; 
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref14">Ghazy et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref20">Li et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref42">Wang et al., 2025</xref>). Under drought stress, SRL1/SRL2 mutants reduce stomatal density, conductance, and transpiration, thereby minimizing water loss (
                    <xref ref-type="bibr" rid="ref22">Liao et al., 2019</xref>). Hormonal treatments, such as kinetin and jasmonate, further improve chlorophyll retention, osmotic adjustment, and spikelet hydration under drought and heat stress (
                    <xref ref-type="bibr" rid="ref47">Yang &amp; Zhang, 2020</xref>; 
                    <xref ref-type="bibr" rid="ref14">Ghazy et al., 2023</xref>).</p>
                <fig fig-type="figure" id="f3" orientation="portrait" position="float">
                    <label>Fig 3. </label>
                    <caption>
                        <title>Mechanisms of stress tolerance in CMS-based hybrid rice.</title>
                    </caption>
                    <graphic id="gr3" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/202622/c3506595-9b10-4013-b9f6-1fddb53034e4_figure3.gif"/>
                </fig>
                <p>Stress adaptation is also supported by maintenance of carbohydrate homeostasis and enhanced antioxidant activity. The sterile line Dexiang 074A maintained soluble sugar content and panicle dry matter allocation under drought conditions, while the restorer line R996 preserved soluble sugars and starch reserves during heat stress, supporting osmoprotection and metabolic stability (
                    <xref ref-type="bibr" rid="ref20">Li et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref52">Zhou et al., 2025</xref>). Increased activities of ascorbic acid (AsA), superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), and ascorbate peroxidase (APX) reduce ROS accumulation and oxidative damage under stress conditions (
                    <xref ref-type="bibr" rid="ref22">Liao et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref48">You et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref42">Wang et al., 2025</xref>). Application of methyl jasmonate (MeJA) further strengthens antioxidant defense by enhancing AsA and CAT activity, thereby protecting reproductive tissues from heat-induced injury (
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>).</p>
                <p>At the molecular level, stress tolerance is regulated through gene expression and QTL introgression. The DRO1 gene promotes deep root development under drought stress, while qDTY1.1, qDTY12.1, and qSDT12&#x2013;2 contribute to maintaining plant architecture and yield stability under water limitation (
                    <xref ref-type="bibr" rid="ref25">Luo et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref30">Nabi et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref31">Nagaraju et al., 2023</xref>). Heat tolerance is strongly associated with heat shock proteins (HSPs), including OsHSP1, cHsp70&#x2013;1, OsHsp17.9A, and OsHSP60-3B, which stabilize proteins and reduce oxidative damage, thereby preserving pollen viability under high temperatures (
                    <xref ref-type="bibr" rid="ref23">Lin et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref52">Zhou et al., 2025</xref>).</p>
                <p>Under salinity stress, the qDYST-1 locus and SKC1NB allele regulate transcriptional responses and Na&#x00a0;+&#x00a0;transport to reduce ion toxicity (
                    <xref ref-type="bibr" rid="ref9">Ding et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref32">Niu et al., 2025</xref>). Tolerance to phosphorus deficiency is associated with qRN5, qRDW5, qRL6, and Pup1, which improve root development and phosphorus uptake efficiency (
                    <xref ref-type="bibr" rid="ref3">Anis et al., 2018</xref>; 
                    <xref ref-type="bibr" rid="ref26">Madhusudan et al., 2022</xref>). Cold tolerance remains comparatively underexplored, although the Cold1 gene has been identified as a regulator of low-temperature sensing through Ca2&#x00a0;+&#x00a0;&#x2013;dependent signaling pathways involving RGA1 (
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>). Overall, these findings demonstrate that modern CMS-based hybrid rice breeding increasingly integrates physiological adaptation with molecular and genomic regulation to enhance stress resilience and yield stability under adverse environments.</p>
            </sec>
            <sec id="sec10">
                <title>3.4 Relationships between abiotic stress, adaptive traits, and yield performance in hybrid Rice</title>
                <p>CMS-based hybrid rice exhibits coordinated morphological, physiological, and reproductive adaptations to abiotic stress (
                    <xref ref-type="fig" rid="f4">
Figure 4</xref>), with drought and heat stress representing the most extensively studied constraints. Drought tolerance is primarily associated with enhanced root architecture, seminal root length, biomass accumulation, and seedling vigor, which collectively improve water uptake and sustain vegetative growth under limited water availability (
                    <xref ref-type="bibr" rid="ref44">Widyastuti et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref18">Hong-Bing et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref22">Liao et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref25">Luo et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref30">Nabi et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref14">Ghazy et al., 2023</xref>). In contrast, heat stress predominantly disrupts reproductive processes, including spikelet fertility, pollen viability, another development, and seed set formation, with spikelet fertility consistently identified as the principal determinant of yield stability under high-temperature conditions (
                    <xref ref-type="bibr" rid="ref49">Zhang et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref23">Lin et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref48">You et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>; 
                    <xref ref-type="bibr" rid="ref52">Zhou et al., 2025</xref>). Salinity, phosphorus deficiency, and cold stress remain comparatively less explored but are generally linked to changes in root development, biomass accumulation, seedling vigor, and reproductive performance (
                    <xref ref-type="bibr" rid="ref3">Anis et al., 2018</xref>; 
                    <xref ref-type="bibr" rid="ref40">Thummala et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref32">Niu et al., 2025</xref>).</p>
                <fig fig-type="figure" id="f4" orientation="portrait" position="float">
                    <label>Fig 4. </label>
                    <caption>
                        <title>Conceptual framework of stress-adaptive traits associated with grain yield and breeding performance in CMS-based hybrid rice.</title>
                    </caption>
                    <graphic id="gr4" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/202622/c3506595-9b10-4013-b9f6-1fddb53034e4_figure4.gif"/>
                </fig>
                <p>
Despite these adaptive responses, physiological tolerance does not always translate into superior productivity, indicating a complex relationship between stress-resilient traits and agronomic performance. Several drought-tolerant hybrids with improved germination and root traits, for example, did not consistently achieve high grain yields, while maintaining reproductive viability under heat stress was sometimes insufficient to sustain seed production (
                    <xref ref-type="bibr" rid="ref44">Widyastuti et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>). In addition, stress-responsive traits are frequently governed by non-additive gene action, reflected by high specific combining ability (SCA) and strong heterotic effects, emphasizing the importance of parental genetic interactions and optimal hybrid combinations in the development of climate-resilient hybrid rice (
                    <xref ref-type="bibr" rid="ref44">Widyastuti et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref33">Pang et al., 2017</xref>).</p>
            </sec>
            <sec id="sec11">
                <title>3.5 Breeding strategies for developing stress-tolerant hybrid rice</title>
                <p>Based on the reviewed studies, hybrid rice breeding strategies are increasingly directed toward developing abiotic stress-tolerant genotypes while maintaining high yield potential. As shown in 
                    <xref ref-type="fig" rid="f5">
Figure 5</xref>, the three-line system remains the dominant breeding approach because of its stable male sterility and well-established seed production system. However, its effectiveness is constrained by the limited availability of compatible restorer lines, leading recent breeding efforts to focus on improving both fertility restoration and stress tolerance simultaneously (
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>). Restorer lines, therefore, serve not only as fertility recoverers but also as important sources of adaptive traits under stress conditions (
                    <xref ref-type="bibr" rid="ref38">Sravanraju et al., 2024</xref>; 
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>; 
                    <xref ref-type="bibr" rid="ref7">Bhuyan et al., 2025</xref>). Drought-tolerant restorers were reported to maintain fertility and productivity under water-deficit conditions (
                    <xref ref-type="bibr" rid="ref31">Nagaraju et al., 2023</xref>), while Guihui5501 combined high yield, grain quality, and cold tolerance (
                    <xref ref-type="bibr" rid="ref43">Wei et al., 2024</xref>).</p>
                <fig fig-type="figure" id="f5" orientation="portrait" position="float">
                    <label>Fig 5. </label>
                    <caption>
                        <title>The relationship between breeding strategies and approaches to developing hybrid rice tolerant to abiotic stress.</title>
                    </caption>
                    <graphic id="gr5" orientation="portrait" position="float" xlink:href="https://f1000research-files.f1000.com/manuscripts/202622/c3506595-9b10-4013-b9f6-1fddb53034e4_figure5.gif"/>
                </fig>
                <p>The development of stress-tolerant hybrids is also strongly influenced by parental combining ability. General combining ability (GCA) and specific combining ability (SCA) analyses are widely used to identify superior hybrid combinations under stress environments. Several studies reported strong SCA effects for drought-tolerant hybrids rice (
                    <xref ref-type="bibr" rid="ref44">Widyastuti et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref11">El-mowafi et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref6">Awad-allah et al., 2022</xref>), whereas IL50&#x2013;13 was identified as a promising salinity-tolerant restorer with favorable combining ability for yield traits (
                    <xref ref-type="bibr" rid="ref40">Thummala et al., 2022</xref>). These findings indicate that non-additive genetic interactions between parental lines largely govern stress tolerance in hybrid rice.</p>
                <p>To accelerate breeding efficiency, molecular approaches are increasingly integrated into hybrid rice improvement programs. Marker-assisted selection targeting fertility restoration genes such as Rf3 and Rf4 has been widely applied for identifying stress-tolerant parental lines (
                    <xref ref-type="bibr" rid="ref36">Priyadarshi et al., 2025</xref>), while QTL introgression remains the primary strategy for improving tolerance to drought, salinity, heat, and phosphorus deficiency (
                    <xref ref-type="bibr" rid="ref3">Anis et al., 2018</xref>; 
                    <xref ref-type="bibr" rid="ref25">Luo et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref1">Abdelrahman et al., 2021</xref>; 
                    <xref ref-type="bibr" rid="ref7">Bhuyan et al., 2025</xref>; 
                    <xref ref-type="bibr" rid="ref32">Niu et al., 2025</xref>). More advanced technologies, including whole-genome sequencing and CRISPR/Cas9-based genome editing, are further enhancing the precision of stress-tolerance improvement and accelerating the development of resilient hybrid rice varieties adapted to changing environmental conditions (
                    <xref ref-type="bibr" rid="ref40">Thummala et al., 2022</xref>; 
                    <xref ref-type="bibr" rid="ref37">Sheng et al., 2023</xref>).</p>
            </sec>
            <sec id="sec12">
                <title>3.6 Challenges and future perspectives</title>
                <p>Although significant progress has been made in developing abiotic stress-tolerant hybrid rice through CMS-based systems, maintaining stable sterility expression and fertility restoration under stress conditions remains a major challenge, particularly under high-temperature stress, which severely disrupts reproductive development and spikelet fertility (
                    <xref ref-type="bibr" rid="ref44">Widyastuti et al., 2017</xref>; 
                    <xref ref-type="bibr" rid="ref8">Chen et al., 2021</xref>). Most existing studies also focus on single-stress tolerance, whereas combined-stress responses and environmental stability remain insufficiently explored. 
                    <xref ref-type="bibr" rid="ref33">Pang et al. (2017)</xref>. demonstrated the potential of DMS-assisted recurrent selection for developing drought- and salinity-tolerant lines, although evaluations were still conducted under limited environmental conditions.</p>
                <p>Another key limitation is the weak integration between molecular breeding and agronomic management. Molecular studies largely emphasise QTL mapping, introgression breeding, and candidate gene identification for stress tolerance (
                    <xref ref-type="bibr" rid="ref3">Anis et al., 2018</xref>; (
                    <xref ref-type="bibr" rid="ref40">Thummala et al., 2022</xref>), whereas agronomic approaches, such as growth regulator applications, are generally investigated separately (
                    <xref ref-type="bibr" rid="ref14">Ghazy et al., 2023</xref>; 
                    <xref ref-type="bibr" rid="ref17">Hamad et al., 2023</xref>). This indicates the need for more integrated strategies that combine molecular genetics, plant physiology, and crop management to simultaneously improve stress tolerance, yield stability, and hybrid seed production efficiency.</p>
                <p>Future progress in stress-tolerant hybrid rice breeding will likely depend on the utilisation of novel germplasm and advanced genomic technologies. Wild rice species such as Oryza rufipogon provide valuable sources of adaptive alleles for drought and salinity tolerance (
                    <xref ref-type="bibr" rid="ref25">Luo et al., 2019</xref>; 
                    <xref ref-type="bibr" rid="ref40">Thummala et al., 2022</xref>), while whole-genome sequencing and genome editing offer opportunities for precise identification and transfer of stress-responsive genes. These advances could accelerate the development of climate-resilient hybrid rice that maintains fertility, productivity, and stability under increasingly complex environmental conditions. Accordingly, future research should prioritise multi-location and multi-season evaluations, combined-stress analyses, and the development of environmentally stable sterility systems to support sustainable hybrid rice production under climate change
                    <bold>.</bold>
                </p>
            </sec>
        </sec>
        <sec id="sec13" sec-type="conclusion">
            <title>4. Conclusion</title>
            <p>The reviewed studies demonstrate that CMS-based hybrid rice breeding remains the most effective and widely adopted strategy for improving rice productivity under abiotic stress conditions. The dominance of WA-CMS and related three-line systems highlights their continued importance in ensuring stable hybrid seed production, efficient fertility restoration, and high yield performance. Advances in physiological, molecular, and genomic research have substantially improved the understanding of stress adaptation mechanisms associated with drought, heat, salinity, nutrient deficiency, and low-temperature tolerance. These mechanisms involve coordinated regulation of water-use efficiency, antioxidant defense, carbohydrate metabolism, root system architecture, and stress-responsive gene expression, collectively contributing to improved resilience and yield stability under adverse environments.</p>
            <p>The review further demonstrates that integrating elite CMS lines, superior restorer germplasm, QTL introgression, and genomics-assisted breeding approaches has accelerated the development of stress-tolerant hybrid rice. Increasing application of molecular markers, high-throughput genotyping, whole-genome sequencing, and genome-editing technologies reflects the transition from conventional phenotype-based breeding toward precision breeding frameworks with greater selection efficiency and predictive accuracy. In particular, the strategic role of restorer lines and non-additive genetic effects emphasizes the importance of parental interactions in maximizing heterosis and environmental adaptability in hybrid rice systems.</p>
            <p>Despite these advances, important limitations remain, including the narrow genetic diversity of CMS and restorer lines, instability of sterility expression under environmental fluctuations, and the limited evaluation of combined-stress responses across diverse field conditions. Therefore, future hybrid rice breeding should prioritize the development of multi-stress-tolerant genotypes, environmentally stable sterility systems, and broader germplasm utilization integrated with advanced genomic technologies. Such approaches will be essential for developing climate-resilient hybrid rice that maintains fertility, productivity, and yield stability under increasingly unpredictable environmental conditions and future climate change scenarios.</p>
        </sec>
    </body>
    <back>
        <sec id="sec16" sec-type="data-availability">
            <title>Data availability statement</title>
            <sec id="sec17">
                <title>Underlying data</title>
                <p>OSF: [
                    <italic toggle="yes">Dataset on Male Sterility Systems in Hybrid Rice for Abiotic Stress Tolerance</italic>]. 
                    <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.17605/OSF.IO/YCKQG">https://doi.org/10.17605/OSF.IO/YCKQG</ext-link> (
                    <xref ref-type="bibr" rid="ref28">Mustaina, 2026a</xref>). The repository is available under the 
                    <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/publicdomain/zero/1.0/legalcode">CC0 1.0 Universal</ext-link>. The project contains the following underlying data:
                    <list list-type="bullet">
                        <list-item>
                            <label>&#x2022;</label>
                            <p>Dataset documenting the screening process, including authors, article titles, source links, abstracts, screening decisions, and reasons for exclusion.</p>
                        </list-item>
                        <list-item>
                            <label>&#x2022;</label>
                            <p>Primary studies included in the final qualitative synthesis and used as the evidence base for the literature review.</p>
                        </list-item>
                        <list-item>
                            <label>&#x2022;</label>
                            <p>PRISMA flowchart illustrating the literature selection process, including the number of articles identified, screened, assessed for eligibility, and included in the final synthesis according to PRISMA guidelines.</p>
                        </list-item>
                    </list>
                </p>
            </sec>
            <sec id="sec18">
                <title>Extended data</title>
                <p>OSF: [
                    <italic toggle="yes">Extended Data on Male Sterility Systems in Hybrid Rice for Abiotic Stress Tolerance and Yield Performance</italic>]. 
                    <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.17605/OSF.IO/XTZ5G">https://doi.org/10.17605/OSF.IO/XTZ5G</ext-link> (
                    <xref ref-type="bibr" rid="ref29">Mustaina, 2026b</xref>). The repository is available under the 
                    <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/publicdomain/zero/1.0/legalcode">CC0 1.0 Universal</ext-link>. This project contains the following extended data:
                    <list list-type="bullet">
                        <list-item>
                            <label>&#x2022;</label>
                            <p>Completed PRISMA 2020 checklist indicating the location of each reporting item addressed in the manuscript.</p>
                        </list-item>
                        <list-item>
                            <label>&#x2022;</label>
                            <p>Evidence matrix summarizing physiological, biochemical, molecular, and agronomic mechanisms associated with abiotic stress tolerance in CMS-based hybrid rice, synthesized from the studies included in this review.</p>
                        </list-item>
                        <list-item>
                            <label>&#x2022;</label>
                            <p>Evidence matrix summarizing the relationships among abiotic stress factors, adaptive traits, and yield performance in CMS-based hybrid rice based on the synthesized evidence from the reviewed studies.</p>
                        </list-item>
                        <list-item>
                            <label>&#x2022;</label>
                            <p>Evidence matrix summarizing breeding strategies and conceptual frameworks proposed for enhancing abiotic stress tolerance and yield performance in CMS-based hybrid rice.</p>
                        </list-item>
                    </list>
                </p>
                <p>Data are available under the terms of the 
                    <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">Creative Commons Zero "No rights reserved" data waiver</ext-link> 

                    <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/publicdomain/zero/1.0/legalcode">(CC0 1.0 Public domain dedication</ext-link>).</p>
            </sec>
            <sec id="sec19">
                <title>Reporting Guidelines</title>
                <p>This systematic review was conducted and reported in accordance with the PRISMA 2020 guidelines.</p>
            </sec>
        </sec>
        <ack>
            <title>Acknowledgments</title>
            <p>The authors gratefully acknowledge the financial support provided by the Indonesia Endowment Fund for Education (Lembaga Pengelola Dana Pendidikan/LPDP), Ministry of Finance of the Republic of Indonesia, for supporting the master&#x2019;s research on which this article is based.</p>
        </ack>
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