A translocation between chromosome 6 and 8 influences lncRNA_MYB114 and PpRPP13 expression and underpins red leaf trait and powdery mildew resistance in peach
{"title":"A translocation between chromosome 6 and 8 influences lncRNA_MYB114 and PpRPP13 expression and underpins red leaf trait and powdery mildew resistance in peach","authors":"Shihang Sun, Junren Meng, Wenjun Zhang, Ang Li, Liang Niu, Lei Pan, Wenyi Duan, Jia-Long Yao, Guochao Cui, Zhiqiang Wang, Wenfang Zeng","doi":"10.1111/nph.70028","DOIUrl":null,"url":null,"abstract":"<p>\n</p><ul>\n<li>Red leaf peach has important ornamental value owing to its characteristic leaf coloration. However, this species is highly susceptible to powdery mildew, and the mechanisms of red leaf formation, resistance to powdery mildew, and their relationship remain unclear.</li>\n<li>We performed population genetic analyses of red leaf peach, revealing that the translocation of chromosomes 6 and 8 is genetically linked to both the red leaf trait and powdery mildew resistance. Bulk segregant analysis-sequencing, genome resequencing, and expression analysis indicated that the <i>PpMYB114</i> and the resistance gene <i>PpRPP13</i> are responsible for the red leaf phenotype and powdery mildew resistance, respectively.</li>\n<li>The chromosomal translocation causes a promoter fragment of <i>PpRPP13</i> on chromosome 8 to integrate into the antisense chain of <i>PpMYB114</i> on chromosome 6, thereby enhancing the expression of <i>PpMYB114</i> and inhibiting the expression of <i>PpRPP13</i>. Further, lncRNA-seq identified a new antisense lncRNA, <i>lncRNA_MYB114</i>, which is generated by the translocation and can activate <i>PpMYB114</i> expression to synthesize anthocyanin. Moreover, the overexpression of <i>PpRPP13</i> resulted in enhanced resistance to powdery mildew.</li>\n<li>In summary, these results revealed the molecular mechanism of a chromosomal translocation altering the expression of <i>PpMYB114</i> and <i>PpRPP13</i> to form the red leaf phenotype that is linked to powdery mildew susceptibility.</li>\n</ul><p></p>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"2 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70028","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Red leaf peach has important ornamental value owing to its characteristic leaf coloration. However, this species is highly susceptible to powdery mildew, and the mechanisms of red leaf formation, resistance to powdery mildew, and their relationship remain unclear.
We performed population genetic analyses of red leaf peach, revealing that the translocation of chromosomes 6 and 8 is genetically linked to both the red leaf trait and powdery mildew resistance. Bulk segregant analysis-sequencing, genome resequencing, and expression analysis indicated that the PpMYB114 and the resistance gene PpRPP13 are responsible for the red leaf phenotype and powdery mildew resistance, respectively.
The chromosomal translocation causes a promoter fragment of PpRPP13 on chromosome 8 to integrate into the antisense chain of PpMYB114 on chromosome 6, thereby enhancing the expression of PpMYB114 and inhibiting the expression of PpRPP13. Further, lncRNA-seq identified a new antisense lncRNA, lncRNA_MYB114, which is generated by the translocation and can activate PpMYB114 expression to synthesize anthocyanin. Moreover, the overexpression of PpRPP13 resulted in enhanced resistance to powdery mildew.
In summary, these results revealed the molecular mechanism of a chromosomal translocation altering the expression of PpMYB114 and PpRPP13 to form the red leaf phenotype that is linked to powdery mildew susceptibility.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.