{"title":"Recessive epistasis of a synonymous mutation confers cucumber domestication through epitranscriptomic regulation","authors":"Tongxu Xin, Zhen Zhang, Yueying Zhang, Xutong Li, Shenhao Wang, Guanqun Wang, Haoxuan Li, Bowen Wang, Mengzhuo Zhang, Wenjing Li, Haojie Tian, Zhonghua Zhang, Yu-Lan Xiao, Weixin Tang, Chuan He, Yiliang Ding, Sanwen Huang, Xueyong Yang","doi":"10.1016/j.cell.2025.06.007","DOIUrl":null,"url":null,"abstract":"Synonymous mutations, once known as “silent” mutations, are increasingly attracting the interest of biologists. Although they may affect transcriptional or post-transcriptional processes, their impact on biological traits remains under-investigated, particularly at the organismal level. Here, we identified two closely linked, epistatically interacting genes: <em>YTH1</em>, an RNA <em>N</em><sup>6</sup>-methyladenosine (m<sup>6</sup>A) reader, and <em>ACS2</em>, an <em>aminocyclopropane-1-carboxylic acid</em> (ACC) synthase, which contribute to cucumber fruit length domestication. The causative mutation in <em>ACS2</em> is a synonymous substitution at 1287C>T. In wild cucumber, <em>ACS2</em><sup><em>1287C</em></sup> results in m<sup>6</sup>A modification on nearby adenosine residues and the formation of loose RNA structural conformations. YTH1 recognizes the m<sup>6</sup>A modification, alters the folding equilibrium toward the weakest RNA structural conformation, and increases the <em>ACS2</em> protein level, resulting in shorter fruit. In cultivated cucumber, <em>ACS2</em><sup><em>1287T</em></sup> disrupts m<sup>6</sup>A methylation and forms compact RNA structural conformations, leading to attenuated protein production and fruit elongation. This study provides genetic evidence of synonymous variation shaping a biological trait through epitranscriptomic regulations.","PeriodicalId":9656,"journal":{"name":"Cell","volume":"27 1","pages":""},"PeriodicalIF":42.5000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cell.2025.06.007","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Synonymous mutations, once known as “silent” mutations, are increasingly attracting the interest of biologists. Although they may affect transcriptional or post-transcriptional processes, their impact on biological traits remains under-investigated, particularly at the organismal level. Here, we identified two closely linked, epistatically interacting genes: YTH1, an RNA N6-methyladenosine (m6A) reader, and ACS2, an aminocyclopropane-1-carboxylic acid (ACC) synthase, which contribute to cucumber fruit length domestication. The causative mutation in ACS2 is a synonymous substitution at 1287C>T. In wild cucumber, ACS21287C results in m6A modification on nearby adenosine residues and the formation of loose RNA structural conformations. YTH1 recognizes the m6A modification, alters the folding equilibrium toward the weakest RNA structural conformation, and increases the ACS2 protein level, resulting in shorter fruit. In cultivated cucumber, ACS21287T disrupts m6A methylation and forms compact RNA structural conformations, leading to attenuated protein production and fruit elongation. This study provides genetic evidence of synonymous variation shaping a biological trait through epitranscriptomic regulations.
期刊介绍:
Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO).
The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries.
In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.