Zhen Gao, Yifan Su, Yaru Wang, Yeqi Li, Yue Wu, Xinru Sun, Yuxin Yao, Chao Ma, Jing Li, Yuanpeng Du
{"title":"The antisense CircRNA VvcircABH controls salt tolerance and the brassinosteroid signaling response by suppressing cognate mRNA splicing in grape","authors":"Zhen Gao, Yifan Su, Yaru Wang, Yeqi Li, Yue Wu, Xinru Sun, Yuxin Yao, Chao Ma, Jing Li, Yuanpeng Du","doi":"10.1111/nph.20306","DOIUrl":null,"url":null,"abstract":"<p>\n</p><ul>\n<li>Soil salinization is a major factor limiting the sustainable development of the grape industry. Circular RNAs (circRNAs) are more stable than linear mRNAs and are involved in stress responses. However, the biological functions and molecular mechanisms underlying antisense circRNAs in plants remain unclear.</li>\n<li>We identified the antisense circRNA <i>VvcircABH</i> through high-throughput sequencing. Using genetic transformation methods and molecular biological techniques, we analyzed the effects of <i>VvcircABH</i> on the response to salt stress and the mechanisms underlying its effects.</li>\n<li><i>VvcircABH</i> was located in the nucleus and upregulated by salt stress, while the expression level of its cognate gene <i>VvABH</i> (alpha/beta-hydrolase) was downregulated. <i>VvcircABH</i> overexpression or <i>VvABH</i> silencing greatly enhanced grape salt tolerance. <i>VvcircABH</i> could bind to the overlapping region and inhibits <i>VvABH</i> pre-mRNA splicing, thereby decreasing the expression level of <i>VvABH</i>. Additionally, <i>VvcircABH</i> repressed the additive effect of VvABH on the interaction between VvBRI1 (brassinosteroid-insensitive 1) and VvBKI1 (BRI1 kinase inhibitor 1), thus influencing the plant's response to BR, which plays important roles in plant salt tolerance.</li>\n<li>We conclude that <i>VvcircABH</i> and <i>VvABH</i> play distinct roles in the salt tolerance and brassinosteroid signaling response, and <i>VvcircABH</i> could govern the expression of <i>VvABH</i> by inhibiting its splicing.</li>\n</ul><p></p>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"59 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-12-03","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.20306","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
Soil salinization is a major factor limiting the sustainable development of the grape industry. Circular RNAs (circRNAs) are more stable than linear mRNAs and are involved in stress responses. However, the biological functions and molecular mechanisms underlying antisense circRNAs in plants remain unclear.
We identified the antisense circRNA VvcircABH through high-throughput sequencing. Using genetic transformation methods and molecular biological techniques, we analyzed the effects of VvcircABH on the response to salt stress and the mechanisms underlying its effects.
VvcircABH was located in the nucleus and upregulated by salt stress, while the expression level of its cognate gene VvABH (alpha/beta-hydrolase) was downregulated. VvcircABH overexpression or VvABH silencing greatly enhanced grape salt tolerance. VvcircABH could bind to the overlapping region and inhibits VvABH pre-mRNA splicing, thereby decreasing the expression level of VvABH. Additionally, VvcircABH repressed the additive effect of VvABH on the interaction between VvBRI1 (brassinosteroid-insensitive 1) and VvBKI1 (BRI1 kinase inhibitor 1), thus influencing the plant's response to BR, which plays important roles in plant salt tolerance.
We conclude that VvcircABH and VvABH play distinct roles in the salt tolerance and brassinosteroid signaling response, and VvcircABH could govern the expression of VvABH by inhibiting its splicing.
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.