{"title":"Integrative GWAS and transcriptomics reveal <i>GhAMT2</i> as a key regulator of cotton resistance to <i>Verticillium wilt</i>.","authors":"Long Wang, Yonglin Yang, Jianghong Qin, Qifeng Ma, Kaikai Qiao, Shuli Fan, Yanying Qu","doi":"10.3389/fpls.2025.1563466","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Verticillium wilt, incited by the soilborne fungus <i>Verticillium dahliae</i>, is a severe threat to global cotton (<i>Gossypium</i> spp.) production, resulting in significant yield losses and reduced fiber quality.</p><p><strong>Methods: </strong>To uncover the genetic and molecular basis of resistance to this devastating disease, we combined genome-wide association study (GWAS) and transcriptomic analyses in a natural population of 355 upland cotton accessions.</p><p><strong>Results: </strong>GWAS identified a stable major-effect quantitative trait locus (QTL), <i>qVW-A01-2</i>, on chromosome A01, which harbors the candidate gene <i>GhAMT2</i>, encoding a high-affinity ammonium transporter. Transcriptomic profiling revealed that <i>GhAMT2</i> was significantly upregulated at 12 hours post-inoculation with <i>V. dahliae</i>, coinciding with the activation of immune signaling pathways. Weighted Gene Co-expression Network Analysis (WGCNA) further linked <i>GhAMT2</i> to critical defense pathways, including lignin biosynthesis, salicylic acid signaling, and reactive oxygen species (ROS) homeostasis, suggesting its role in cell wall reinforcement and systemic immune responses. Functional validation through virus-induced gene silencing (VIGS) confirmed that silencing <i>GhAMT2</i> compromised disease resistance. In contrast, transgenic Arabidopsis plants overexpressing <i>GhAMT2</i> exhibited enhanced resistance to <i>V. dahliae</i>, demonstrating its essential role in defense regulation.</p><p><strong>Discussion: </strong>These findings establish <i>GhAMT2</i> as a key regulator of cotton resistance to Verticillium wilt and highlight its potential for marker-assisted breeding and genetic engineering to improve disease-resistant cotton varieties.</p>","PeriodicalId":12632,"journal":{"name":"Frontiers in Plant Science","volume":"16 ","pages":"1563466"},"PeriodicalIF":4.1000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12062179/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Plant Science","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fpls.2025.1563466","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Verticillium wilt, incited by the soilborne fungus Verticillium dahliae, is a severe threat to global cotton (Gossypium spp.) production, resulting in significant yield losses and reduced fiber quality.
Methods: To uncover the genetic and molecular basis of resistance to this devastating disease, we combined genome-wide association study (GWAS) and transcriptomic analyses in a natural population of 355 upland cotton accessions.
Results: GWAS identified a stable major-effect quantitative trait locus (QTL), qVW-A01-2, on chromosome A01, which harbors the candidate gene GhAMT2, encoding a high-affinity ammonium transporter. Transcriptomic profiling revealed that GhAMT2 was significantly upregulated at 12 hours post-inoculation with V. dahliae, coinciding with the activation of immune signaling pathways. Weighted Gene Co-expression Network Analysis (WGCNA) further linked GhAMT2 to critical defense pathways, including lignin biosynthesis, salicylic acid signaling, and reactive oxygen species (ROS) homeostasis, suggesting its role in cell wall reinforcement and systemic immune responses. Functional validation through virus-induced gene silencing (VIGS) confirmed that silencing GhAMT2 compromised disease resistance. In contrast, transgenic Arabidopsis plants overexpressing GhAMT2 exhibited enhanced resistance to V. dahliae, demonstrating its essential role in defense regulation.
Discussion: These findings establish GhAMT2 as a key regulator of cotton resistance to Verticillium wilt and highlight its potential for marker-assisted breeding and genetic engineering to improve disease-resistant cotton varieties.
期刊介绍:
In an ever changing world, plant science is of the utmost importance for securing the future well-being of humankind. Plants provide oxygen, food, feed, fibers, and building materials. In addition, they are a diverse source of industrial and pharmaceutical chemicals. Plants are centrally important to the health of ecosystems, and their understanding is critical for learning how to manage and maintain a sustainable biosphere. Plant science is extremely interdisciplinary, reaching from agricultural science to paleobotany, and molecular physiology to ecology. It uses the latest developments in computer science, optics, molecular biology and genomics to address challenges in model systems, agricultural crops, and ecosystems. Plant science research inquires into the form, function, development, diversity, reproduction, evolution and uses of both higher and lower plants and their interactions with other organisms throughout the biosphere. Frontiers in Plant Science welcomes outstanding contributions in any field of plant science from basic to applied research, from organismal to molecular studies, from single plant analysis to studies of populations and whole ecosystems, and from molecular to biophysical to computational approaches.
Frontiers in Plant Science publishes articles on the most outstanding discoveries across a wide research spectrum of Plant Science. The mission of Frontiers in Plant Science is to bring all relevant Plant Science areas together on a single platform.