Jinfang Wang, Yi Zhu, Maoying Li, Haiying Zhang, Xilong Zhang, Shouwei Tian, Yi Ren, Yongtao Yu, Shengjin Liao, Guoyi Gong, Nikolay Velkov, Yong Xu, Jie Zhang
{"title":"NAC转录因子ClNAC100正调控西瓜株高和果实大小","authors":"Jinfang Wang, Yi Zhu, Maoying Li, Haiying Zhang, Xilong Zhang, Shouwei Tian, Yi Ren, Yongtao Yu, Shengjin Liao, Guoyi Gong, Nikolay Velkov, Yong Xu, Jie Zhang","doi":"10.1111/tpj.70292","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Fruit size correlates with yield potential and serves as a vital agronomic trait. However, the key regulatory genes controlling fruit size in watermelon (<i>Citrullus lanatus</i>) remain poorly understood. In this study, we identified a NAC transcription factor gene <i>ClNAC100</i> localized to selective sweep regions that positively regulated plant height and fruit size. CRISPR-Cas9-mediated knockout of <i>ClNAC100</i> caused dramatic reductions in both plant height and fruit size, concomitant with decreased gibberellin (GA) levels in mutants. Exogenous GA<sub>4</sub> application partially rescued the plant height and fruit size of the <i>clnac100</i> mutant, while it could not restore these traits to wild-type levels. ClNAC100 directly upregulated expansin gene <i>ClEXPA1</i> and GA biosynthetic genes <i>ClGA3ox</i>s, though DELLA protein interactions attenuated this transcriptional activation. A natural variant (−1087, T/C) of <i>ClNAC100</i> enabled the Dof transcription factor ClDof4.6 to bind and activate <i>ClNAC100</i> expression during watermelon domestication. Together, our results demonstrate that <i>ClNAC100</i> mainly modulates the GA pathway to regulate fruit size and plant height, advancing mechanistic understanding of these agriculturally critical traits.</p>\n </div>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"123 1","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2025-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The NAC transcription factor ClNAC100 positively regulates plant height and fruit size in watermelon\",\"authors\":\"Jinfang Wang, Yi Zhu, Maoying Li, Haiying Zhang, Xilong Zhang, Shouwei Tian, Yi Ren, Yongtao Yu, Shengjin Liao, Guoyi Gong, Nikolay Velkov, Yong Xu, Jie Zhang\",\"doi\":\"10.1111/tpj.70292\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Fruit size correlates with yield potential and serves as a vital agronomic trait. However, the key regulatory genes controlling fruit size in watermelon (<i>Citrullus lanatus</i>) remain poorly understood. In this study, we identified a NAC transcription factor gene <i>ClNAC100</i> localized to selective sweep regions that positively regulated plant height and fruit size. CRISPR-Cas9-mediated knockout of <i>ClNAC100</i> caused dramatic reductions in both plant height and fruit size, concomitant with decreased gibberellin (GA) levels in mutants. Exogenous GA<sub>4</sub> application partially rescued the plant height and fruit size of the <i>clnac100</i> mutant, while it could not restore these traits to wild-type levels. ClNAC100 directly upregulated expansin gene <i>ClEXPA1</i> and GA biosynthetic genes <i>ClGA3ox</i>s, though DELLA protein interactions attenuated this transcriptional activation. A natural variant (−1087, T/C) of <i>ClNAC100</i> enabled the Dof transcription factor ClDof4.6 to bind and activate <i>ClNAC100</i> expression during watermelon domestication. Together, our results demonstrate that <i>ClNAC100</i> mainly modulates the GA pathway to regulate fruit size and plant height, advancing mechanistic understanding of these agriculturally critical traits.</p>\\n </div>\",\"PeriodicalId\":233,\"journal\":{\"name\":\"The Plant Journal\",\"volume\":\"123 1\",\"pages\":\"\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2025-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Plant Journal\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/tpj.70292\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.70292","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
The NAC transcription factor ClNAC100 positively regulates plant height and fruit size in watermelon
Fruit size correlates with yield potential and serves as a vital agronomic trait. However, the key regulatory genes controlling fruit size in watermelon (Citrullus lanatus) remain poorly understood. In this study, we identified a NAC transcription factor gene ClNAC100 localized to selective sweep regions that positively regulated plant height and fruit size. CRISPR-Cas9-mediated knockout of ClNAC100 caused dramatic reductions in both plant height and fruit size, concomitant with decreased gibberellin (GA) levels in mutants. Exogenous GA4 application partially rescued the plant height and fruit size of the clnac100 mutant, while it could not restore these traits to wild-type levels. ClNAC100 directly upregulated expansin gene ClEXPA1 and GA biosynthetic genes ClGA3oxs, though DELLA protein interactions attenuated this transcriptional activation. A natural variant (−1087, T/C) of ClNAC100 enabled the Dof transcription factor ClDof4.6 to bind and activate ClNAC100 expression during watermelon domestication. Together, our results demonstrate that ClNAC100 mainly modulates the GA pathway to regulate fruit size and plant height, advancing mechanistic understanding of these agriculturally critical traits.
期刊介绍:
Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community.
Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.