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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Plant Sci.</journal-id>
<journal-title>Frontiers in Plant Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Plant Sci.</abbrev-journal-title>
<issn pub-type="epub">1664-462X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpls.2024.1369070</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Plant Science</subject>
<subj-group>
<subject>Editorial</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Editorial: Plant reproduction under environmental stress</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Begcy</surname>
<given-names>Kevin</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/614412"/>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
<xref ref-type="author-notes" rid="fn003">
<sup>&#x2020;</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mendes</surname>
<given-names>Marta A.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/555812"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>De Storme</surname>
<given-names>Nico</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/91829"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Environmental Horticulture Department, University of Florida</institution>, <addr-line>Gainesville, FL</addr-line>, <country>United States</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Plant Molecular and Cellular Biology Graduate Program, University of Florida</institution>, <addr-line>Gainesville, FL</addr-line>, <country>United States</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Dipartimento di Bioscienze, Universit&#xe0; degli Studi di Milano</institution>, <addr-line>Milan</addr-line>, <country>Italy</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Laboratory for Plant Genetics and Crop Improvement, Division of Crop Biotechnics, Department of Biosystems</institution>, <addr-line>Heverlee, KU Leuven</addr-line>, <country>Belgium</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Manuel Nieves-Cordones, Spanish National Research Council (CSIC), Spain</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Kevin Begcy, <email xlink:href="mailto:kbegcy.padilla@ufl.edu">kbegcy.padilla@ufl.edu</email>
</p>
</fn>
<fn fn-type="other" id="fn003">
<p>&#x2020;ORCID: Kevin Begcy, <uri xlink:href="https://orcid.org/0000-0002-5046-8029">orcid.org/0000-0002-5046-8029</uri>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>26</day>
<month>02</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1369070</elocation-id>
<history>
<date date-type="received">
<day>11</day>
<month>01</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>07</day>
<month>02</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Begcy, Mendes and De Storme</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Begcy, Mendes and De Storme</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>    <related-article id="RA1" related-article-type="commentary-article" xlink:href="https://www.frontiersin.org/researchtopic/20093" ext-link-type="uri">Editorial on the Research Topic <article-title>Plant reproduction under environmental stress</article-title>
</related-article>
<kwd-group>
<kwd>flowering transition</kwd>
<kwd>ovule</kwd>
<kwd>pollen</kwd>
<kwd>seeds</kwd>
<kwd>stress responses</kwd>
<kwd>heat</kwd>
<kwd>cold</kwd>
<kwd>epigenetics</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="8"/>
<page-count count="3"/>
<word-count count="1610"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Plant Abiotic Stress</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>Reproductive development is an essential phase during the life cycle of flowering plants. It ensures preservation of karyotypic configuration and genomic stability, and additionally creates novel genetic variation in the offspring. In the current context of global warming and climate change, with plants being more intensively challenged by extreme environmental conditions, insights into the sensitivity of the molecular and physiological responses of the reproductive pathway to external stresses are highly relevant for both plant evolution and crop productivity. In this Research Topic, we present the impact of low and high temperatures as well as low light conditions on plant reproduction.</p>
<sec id="s1">
<title>Impact of low temperatures on plant reproduction</title>
<p>For some crops, low temperatures are a serious threat that results in drastic yield decline. Using tomato (<italic>Solanum lycopersicum</italic>) as model plant, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2021.687826">Yang et&#xa0;al.</ext-link> explored whether N6-methyladenosine (m<sup>6</sup>A) regulates pollen development under low temperature stress and found that this condition affects pollen development at the tetrad stage, causing pollen sterility, characterized by changes in tapetum development and exine deposition. m<sup>6</sup>A levels in anthers were decreased at both the tetrad and the uninucleate stages under low temperature stress compared to control conditions. Further transcriptome-wide detection of m<sup>6</sup>A methylation levels in anthers at the tetrad stage under low temperature conditions showed that cold conditions affect m<sup>6</sup>A levels in many predominantly downregulated mRNA transcripts. These differentially m<sup>6</sup>A enriched transcripts under low temperature conditions were mainly related to ATP-binding pathways, adenosine triphosphatase activity, and lipid metabolism. Interestingly, <italic>SlABCG31</italic>, an ATP-binding transcript predominantly expressed in anthers, was proposed to participate in the regulation of abscisic acid (ABA), as its significant m<sup>6</sup>A upregulation was correlated with higher ABA levels in anthers. These interesting findings suggest that the decrease in m<sup>6</sup>A levels in response to low temperatures results in the altered transcription of many pollen development-related genes impacting anther ABA levels, leading to pollen sterility.</p>
<p>Another exciting story comes from a study in which the authors explored the impact of low temperatures on the transition from the vegetative to the reproductive phase (<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.817356">Nasim et&#xa0;al.</ext-link>). This critical developmental transition is primarily regulated by the expression of <italic>FLOWERING LOCUS C</italic> (<italic>FLC</italic>) and other clade-related genes controlled by Polymerase II-Associated Factor 1 Complex (PAF1C - <italic>CELL DIVISION CYCLE73/PLANT HOMOLOGOUS TO PARAFIBROMIN</italic>, <italic>VERNALIZATION INDEPENDENCE2</italic> (<italic>VIP2</italic>)/<italic>EARLY FLOWERING7</italic> (<italic>ELF7</italic>), <italic>VIP3</italic>, <italic>VIP4</italic>, <italic>VIP5</italic>, and <italic>VIP6/ELF8</italic>). In <italic>Arabidopsis thaliana</italic> T-DNA PAF1C-deficient mutant lines, strong early flowering was observed as temperature was decreased. Since changes in epigenetic status have been shown to be critical for the stress response during reproductive development (<xref ref-type="bibr" rid="B1">Begcy and Dresselhaus, 2018</xref>), <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.817356">Nasim et&#xa0;al.</ext-link> analyzed the levels of H3K27me3 and H3K4me3/H3K36me3 marks on <italic>FLC</italic> and the <italic>FLC</italic>-clade genes. Under low temperature stress, <italic>FLC</italic> and <italic>FLC</italic>-clade genes showed significantly increased enrichment of H3K27me3 and significantly reduced enrichment of H3K4me3 marks in PAF1C mutants, which is consistent with their transcriptional downregulation. These results show that PAF1C is required to maintain active histone H3K4me3 marks while preventing the deposition of H3K27me3 repressive marks at the <italic>FLC</italic> and <italic>FLC</italic>-clade genes, thereby maintaining their active transcription.</p>
<p>Another aspect covered in this Research Topic is the effect of low temperatures during the bloom period in grapes and their impact on fruit set. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.864892">Keller et&#xa0;al.</ext-link> manipulated the inflorescence temperature of field-grown Cabernet Sauvignon grapevines during the bloom period. Low temperatures resulted in decreased fruit set, as indicated mainly by the lowest berry number per cluster, as well as seed and berry weight at harvest. At the biochemical level, low temperatures slightly decreased fruit soluble solids and pH, and increased titratable acidity, but did not affect color density. In summary, these results suggest that low temperatures not only decrease the proportion of flowers that set fruit but also limit the sink strength of the berries that do develop after fruit set.</p>
</sec>
<sec id="s2">
<title>Impact of heat stress on plant reproduction</title>
<p>High temperatures caused by climate change are negatively impacting reproductive success in many plant species (<xref ref-type="bibr" rid="B4">De Storme and Geelen, 2014</xref>; <xref ref-type="bibr" rid="B3">Chen et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B2">Begcy et&#xa0;al., 2019</xref>). An understanding of how plants try to overcome heat stress during their reproductive phase is fundamental to the effective design of strategies to improve agricultural productivity. In a well-considered review paper, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2023.1271644">Resentini et&#xa0;al.</ext-link> provided a general overview of the molecular mechanisms underlying heat stress resilience during reproductive development through comparison of a dicotyledonous and a monocotyledonous model system, <italic>Arabidopsis</italic> and <italic>Oryza sativa.</italic> The pollen and the ovule are two reproductive organs whose development is highly susceptible to heat stress. The authors describe four main strands of impact when temperatures are increased during normal development in these two organs: (1) morphological alteration of these tissues, including the anthers and pistils, impacting reproductive success; (2) inhibition of male and female gametophyte development; (3) inhibition of pollen development; and (4) limitation of pollen tube growth. These aspects highlight some of the weakest developmental organs during plant reproduction. Two important additional aspects, summarized by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2023.1271644">Resentini et&#xa0;al.</ext-link>, are recent advances in understanding of the cellular responses to heat stress, represented by the induction of heat shock proteins and calcium signaling. A solid amount of data indicates that heat stress affects plant Ca<sup>2+</sup> channels, inducing a transient increase in cytosolic Ca<sup>2+</sup> concentration. Cytosolic Ca<sup>2+</sup> ion acts as a second messenger that triggers specific cellular responses, including heat shock factors and heat shock proteins. These large groups of transcription factors and chaperones have been used to develop heat resilient crops (<xref ref-type="bibr" rid="B8">ul Haq et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B5">Kim et&#xa0;al., 2021</xref>).</p>
<p>In cucumber (<italic>Cucumis sativus</italic> L.), high temperature stress always results in sterility at the reproductive stage (<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2021.758976">Chen et&#xa0;al.</ext-link>). To elucidate the nature of this susceptibility, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2021.758976">Chen et&#xa0;al.</ext-link> performed cross-section analysis of anther development in cucumber at high temperatures. The authors observed tapetum abnormality, abnormal microspore, and microspore degeneration in stressed anthers. A high rate of pollen grain abortion and a significant reduction in pollen fertility were also demonstrated. When antioxidant enzymatic activity was measured, including peroxidase, malondialdehyde, catalase, and superoxide dismutase, extremely high levels were found in heat-stressed anthers, which indicates a stressed physiological status. Interestingly, transcriptional analysis showed that carbohydrates and many saccharides and starch synthase-related genes, such as invertase, sucrose synthase, and starch-branching enzymes, were misregulated under exposure to increased temperatures, which represents a common stress response in many plant species, as shown in maize, cotton, and Arabidopsis (<xref ref-type="bibr" rid="B2">Begcy et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B6">Masoomi-Aladizgeh et&#xa0;al., 2021</xref>; <xref ref-type="bibr" rid="B7">Seydel et&#xa0;al., 2022</xref>).</p>
<p>Using a combination of invasive and non-invasive techniques to investigate floret development in barley (<italic>Hordeum vulgare</italic>), <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.918730">Callens et&#xa0;al.</ext-link> showed that while female reproductive organs are less susceptible to heat stress, male reproductive organs are severely impacted. A practical conclusion of this study was that the timing of stress relative to reproductive development has a significant impact on fertility in a cultivar-dependent manner. Immunolabelling of cell wall components in anthers and ovules of heat-stressed barley plants showed that anther cell wall components collapsed (including 1,3;1,4-&#x3b2;-glucan, de-esterified homogalacturonan, and cellulose). The immunolabelling of ovule sections showed that the embryo sac was present in all cases, but there seemed to be fewer cell layers between the embryo sac and the integument. However, no obvious irregularities in the morphology of the embryo sac were identified.</p>
<p>In tomato, the meiosis to early microspore stage of pollen development was found to be the most sensitive to heat stress, and only three days of heat exposure during this developmental window was sufficient to significantly reduce pollen viability at the flower anthesis stage. Cytological analysis showed that abnormalities in pollen development could first be observed after pollen mitosis I, while no deviations in tapetum development were observed. At the transcriptional and biochemical level, pollen development suffered from tapetal endoplasmic reticulum stress (<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.925754">Xu et&#xa0;al.</ext-link>).</p>
<p>Heat stress during seed development is a significant factor in reducing seed size and yield. Using <italic>Camelina sativa</italic>, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2023.1284573">Nadakuduti et&#xa0;al.</ext-link> explored the impact of high temperatures on fatty acids. Striking differences in the qualitative and quantitative levels of fatty acids were detected. A decrease in percentage polyunsaturated fatty acids and an increase in percentage monounsaturated accumulation of fatty acids was measured under heat stress conditions. The authors suggested that fatty acid biosynthesis shifted to monounsaturated fatty acid synthesis to protect cell function and embryo development by maintaining membrane stability and preventing fatty acid oxidation.</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.828743">Jansma et&#xa0;al.</ext-link> used a <italic>35S:nahG</italic> tomato line, which has low levels of the stress response-associated hormone salicylic acid, to investigate whether this hormone improves pollen thermotolerance to high temperatures or negatively reduces the investment of resources in reproductive development. Low levels of salicylic acid were found to increase pollen viability under heat stress conditions by enhancing jasmonic acid signaling in developing anthers. These results open the door for alternative pathways within the current biotechnological and breeding strategies that are implemented to ameliorate stress responses.</p>
</sec>
<sec id="s3">
<title>Impact of low light on plant reproduction</title>
<p>Aiming to understand alfalfa (<italic>Medicago sativa</italic> L.) development during reproduction under shading conditions, Quin et&#xa0;al. studied flowering phenology, pollen viability, stigma receptivity, and seed quality. In general, low light conditions delayed flowering phenology, shortened the flowering stage, and significantly reduced pollen viability, stigma receptivity, number of flowers, and quantity and quality of seeds. Interestingly, since alfalfa is a forage crop used in intercropping or rotation ecosystems, low light conditions were beneficial in maintaining a high aboveground biomass (<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.835380">Qin et&#xa0;al.</ext-link>). This is likely due to the regulation of the accumulation and distribution of assimilates between the vegetative and reproductive organs.</p>
</sec>
<sec id="s4" sec-type="author-contributions">
<title>Author contributions</title>
<p>KB: Conceptualization, Writing &#x2013; original draft, Writing &#x2013; review &amp; editing. MM: Writing &#x2013; review &amp; editing. NS: Writing &#x2013; review &amp; editing.</p>
</sec>
</body>
<back>
<sec id="s5" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Experimental work on plant reproduction under environmental stresses in the laboratory of KB is funded by the USDA National Institute of Food and Agriculture NIFA-AFRI program (Grant 2023-67013-39412) and the Global Food Systems Institute.</p>
</sec>
<sec id="s6" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s7" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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