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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.2023.1222818</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: Genomics in plant sciences: understanding and development of stress-tolerant plants</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Dar</surname>
<given-names>Ayaz Mahmood</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1890905"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Touseef</surname>
<given-names>Hussain</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/940727"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nawaz</surname>
<given-names>Kashif</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1997336"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Khan</surname>
<given-names>Yusuf</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/90244"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Sahu</surname>
<given-names>Pranav Pankaj</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/424951"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Organic and Biomolecular Research, Department of Higher Education (GDC Sogam), University of Kashmir</institution>, <addr-line>Srinagar, Jammu and Kashmir</addr-line>, <country>India</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Sevama AgriClinic and Laboratory, MatI Mate Agromart Pvt. Ltd.</institution>, <addr-line>Bhavnagar, Gujarat</addr-line>, <country>India</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Plant Breeding and Genetics, Max Planck Institute for Plant Breeding Research</institution>, <addr-line>K&#xf6;ln</addr-line>, <country>Germany</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Biological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology</institution>, <addr-line>Thuwal</addr-line>, <country>Saudi Arabia</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Newborn Screening Department, University Hospital</institution>, <addr-line>Oslo</addr-line>, <country>Norway</country>
</aff>
<aff id="aff6">
<sup>6</sup>
<institution>Laboratory of Ecological Plant Physiology, Global Change Research Institute of the Czech Academy of Sciences</institution>, <addr-line>Brno</addr-line>, <country>Czechia</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Yi-Hong Wang, University of Louisiana at Lafayette, United States</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Rahul Singh Jasrotia, Indian Council of Agricultural Research, India</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Pranav Pankaj Sahu, <email xlink:href="mailto:sahu.p@czechglobe.cz">sahu.p@czechglobe.cz</email>; Yusuf Khan, <email xlink:href="mailto:yusuf.zhc@gmail.com">yusuf.zhc@gmail.com</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>07</day>
<month>06</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>14</volume>
<elocation-id>1222818</elocation-id>
<history>
<date date-type="received">
<day>15</day>
<month>05</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>26</day>
<month>05</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Dar, Touseef, Nawaz, Khan and Sahu</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Dar, Touseef, Nawaz, Khan and Sahu</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/research-topics/43258" ext-link-type="uri">Editorial on the Research Topic <article-title>Genomics in plant sciences: understanding and development of stress-tolerant plants</article-title>
</related-article>
<kwd-group>
<kwd>genomics</kwd>
<kwd>crop genetics</kwd>
<kwd>breeding</kwd>
<kwd>genome-wide studies</kwd>
<kwd>multi-omics</kwd>
<kwd>abiotic</kwd>
<kwd>biotic</kwd>
<kwd>stress-tolerance</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="5"/>
<page-count count="3"/>
<word-count count="1093"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Functional and Applied Plant Genomics</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>Environmental stresses have a profound impact on the growth and productivity of plants (<xref ref-type="bibr" rid="B2">Boyer, 1982</xref>). The predicted growth of the human population and impending changes in climate could further threaten food availability around the World. Hence, it is of prime importance for researchers across the world to fast-track the development the high-yield stress-tolerant plants. The process requires a deeper understanding of genome structure, and biochemical, physiological, and molecular mechanisms underlying abiotic and biotic stress tolerance in plants. Plants have evolved complex molecular mechanisms to respond to both these stimuli (<xref ref-type="bibr" rid="B1">Bechtold and Field, 2018</xref>). It comprises the recognition of stress factors, activation of the stress signaling cascade, and synthesis of stress-related genes, proteins, or other molecules (<xref ref-type="bibr" rid="B5">Zhang et&#xa0;al., 2020</xref>). Moreover, genomics approaches like genetic diversity analysis, allelic variations identification, phylogenies, and understanding the adaptive evolution of genomes could also serve as vital tools to develop plant varieties mitigating food security issues (<xref ref-type="bibr" rid="B3">Cushman and Bohnert, 2000</xref>). Hence, an extensive effort is needed to utilize the plant genomics resources generated and to identify the key genes and regulators, which can withstand the diverse agroecological conditions/climates. This Research Topic represented the collection of nine original research articles and two reviews signifying the role of genomics, functional genomics, and multi-omics approaches in the development of stress-tolerant plants.</p>
<p>The identification of hotspots in the genomic architecture of plant species by chromosome-scale genome assembly, comparative genomics, and multi-omics approach could assist in mapping stress-associated genes and quantitative trait loci (QTLs). The captured QTLs and SNPs markers in the genome not only provide information about the genomic architecture but could impart stress resilience in plants by marker-assisted selection and breeding. A study done by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2023.1124619">Sarkar et&#xa0;al.</ext-link> on maize successfully mapped the QTLs for the growth- and yield-related traits under water availability scenarios. The genes underlying these QTLs have specific functions in maintaining the growth and senescence, and hormone signaling under water deficit conditions. The nucleotide polymorphism in the promoter elements in rice has been shown to modulate the salt-responsive attributes by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1089109">Haque et&#xa0;al</ext-link>. The comparative sequence analysis of K<sup>+</sup> salt-responsive transporters (<italic>OsTPKa</italic> and <italic>OsHAK</italic>) among two contrasting rice genotypes differed in salt-responsiveness revealing that both have unique TF-binding motifs. These modifications in the elements, played a key role in the coordinated expression of both transports, leading to an effective acclimation response in rice.</p>
<p>The candidate genes and proteins belonging to the flavonoid, phenylpropanoid, and &#x3b1;-linolenic acid metabolism were mapped on the tea (<italic>Camellia sinensis</italic>) genome by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1004387">Wang et&#xa0;al</ext-link>. These potential targets in the tea genome could play an imperative role in the development of tea plants resistant to green leafhopper infestation. A similar approach was also applied to understand the genetic basis of cold adaptation in Asparagus beans by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1059804">Liang et&#xa0;al</ext-link>. In the comparative genomics approach between contrasting bean accessions, a set of variable genes in two individual genomes was retrieved. A detailed analysis of these genes identified that in the genome of cold tolerant accession, Ningjiang 3 the presence of ABCC-type transports (a sub-gene family of ABC transporters) was linked with enhanced abiotic stress resilience.</p>
<p>A massive structural variation in the sesame pan-genome due to evolutionary adaptations was reported by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1076229">Parakkunnel et&#xa0;al</ext-link>. These genetic novelties in APETALA2/Ethylene Responsive Factor (AP2/ERF) and WRKY transcription factors were due to alterations in the copy numbers, shifts in their location, and structural changes in the <italic>cis</italic>-element and exon-intron structure. These transcription factors (TFs) have a very specific role in the regulation of plants&#x2019; defense against environmental stress, hence suggesting the adaptive selection pressure leading to structural variation in the sesame genome. Similarly, the comparative analysis of the chloroplast genome of black pepper (<italic>Piper nigrum L</italic>.) with related piper species was studied by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1095781">Gaikwad et&#xa0;al</ext-link>. The study provided key insights into the chloroplast genome evolution, which will assist in the development of molecular markers and accelerate ongoing black pepper improvement programs.</p>
<p>Moreover, <italic>in-silico</italic> genome-wide analysis of key gene families and their comparative analysis could decipher the biotic and abiotic stress adaptations in plant species. A similar strategy was further exploited by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1043261">Nie et&#xa0;al.</ext-link>, to explore the role of leucine-rich repeat receptor-like kinases (LRR-RLKs) during <italic>Bursaphelenchus xylophilus</italic> infestation in <italic>Pinus massoniana</italic>. The candidate RLK genes retrieved from the transcriptome datasets were subjected to structural and molecular characterization. The study revealed that an LRR XII subfamily gene <italic>PmRLKs32</italic>, having ROS-producing properties played an important role in providing nematode resistance in pine trees. An extensive structural, functional, molecular, and evolutionary study on the Caffeoyl-CoA O-methyltransferase (CCoAOMT) gene family was carried out in two jute species by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1035383">Akhter et&#xa0;al</ext-link>. Despite both species showing high syntenic conservation among <italic>CCoAOMTs</italic>, the gene expression level was modulated among them under various abiotic stresses and hormonal treatment. Hence, the key gene from the CCoAOMT gene family could be used to genetically engineered jute plants that can withstand a wide range of environmental stresses. Though, it is also important to functionally characterize the candidate genes for the required traits. For example, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1013445">Zhang et&#xa0;al.</ext-link>, showed how an MYC TF plays a major role in regulating growth and fruit quality in tomato. Through molecular study, they reported that the interplay between MYC2 and jasmonic acid (JA) and TOR signaling pathways regulates the growth and development of tomato seedlings.</p>
<p>This Research Topic contains two important review articles focused on genetic (structural changes) and epigenetic (reversible changes) modifications in the genome leading to stress adaptations in plants. The retrotransposons are varied in copy number and activated by various biotic and abiotic stresses due to retrotransposition bursts. The review by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1064847">Papolu et&#xa0;al.</ext-link>, focused on the dynamics of LTR retrotransposons and the associated mechanism of genome expression and adaptive evolution during high-temperature stress. The epigenetic changes are transgenerational and important for the stress memories in plants (<xref ref-type="bibr" rid="B4">Sahu et&#xa0;al., 2013</xref>). The review by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fpls.2022.1075279">Ramakrishnan et&#xa0;al.</ext-link>, summarized the regulatory mechanism of memory establishment in plants under cold and heat stress, through histone modification and DNA methylation process.</p>
<p>Overall, the present research studies highlight the importance of genetic and genomic tools in the identification and development of stress-tolerant plants. The progress made towards understanding how structural changes in plant genomes could shape the unique response to environmental stresses will be critical for the improvement of crop plants.</p>
<sec id="s1" sec-type="author-contributions">
<title>Author contributions</title>
<p>All authors have contributed in writing, editing, reading and agreed to the final version of the manuscript.</p>
</sec>
</body>
<back>
<sec id="s2" sec-type="funding-information">
<title>Funding</title>
<p>PPS thanks the Czech Science Foundation, for providing the grant support (Grant no. 20-25845Y).</p>
</sec>
<sec id="s3" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>Author HT was employed by MatI Mate Agromart Pvt. Ltd.</p>
<p>The remaining 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="s4" 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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