{"title":"TIP2-UDT1-OsUPEX1/2 module regulates tapetum development and function in rice","authors":"Ruifeng Wang, Yaqian Sun, Wanlin Liu, Xiaofei Chen, Jie Xu, Zheng Yuan, Wanqi Liang, Dabing Zhang","doi":"10.1111/nph.20435","DOIUrl":null,"url":null,"abstract":"<p>\n</p><ul>\n<li>The tapetum in the anther wall is essential for plant fertility, secreting many components essential for pollen development. Development of the tapetum is controlled by multiple transcription factors and signaling pathways. UDT1, TIP2, TDR, and EAT1 constitute a sequential regulatory cascade crucial for tapetal differentiation in rice, but UDT1- and TIP2-dependent regulatory networks, particularly in early anther development, remain largely unknown.</li>\n<li>Functional analysis of knockout mutants and spatial–temporal expression analysis demonstrated overlapping expression of TIP2 and UDT1 in the middle layer and tapetum and that the <i>tip2</i> mutation was epistatic to <i>udt1</i>. Moreover, TIP2 and UDT1 were shown to heterodimerize to activate the expression of downstream genes essential for early anther development.</li>\n<li>We identified two genes activated by TIP2-UDT1, <i>OsUPEX1</i> and <i>OsUPEX2</i>, predicted to encode galactosyltransferases, that were preferentially expressed in the tapetum. Analysis of their single mutants demonstrated their functional redundancy, while the double knockout mutant revealed their critical roles in tapetum development and function, likely in enabling tapetal secretion.</li>\n<li>Overall, this study provides insights into the regulation of rice anther development by TIP2 and UDT1 and identifies downstream targets <i>OsUPEX1</i> and <i>OsUPEX2</i> essential for tapetum function and rice male fertility.</li>\n</ul><p></p>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"85 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-02-27","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.20435","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
The tapetum in the anther wall is essential for plant fertility, secreting many components essential for pollen development. Development of the tapetum is controlled by multiple transcription factors and signaling pathways. UDT1, TIP2, TDR, and EAT1 constitute a sequential regulatory cascade crucial for tapetal differentiation in rice, but UDT1- and TIP2-dependent regulatory networks, particularly in early anther development, remain largely unknown.
Functional analysis of knockout mutants and spatial–temporal expression analysis demonstrated overlapping expression of TIP2 and UDT1 in the middle layer and tapetum and that the tip2 mutation was epistatic to udt1. Moreover, TIP2 and UDT1 were shown to heterodimerize to activate the expression of downstream genes essential for early anther development.
We identified two genes activated by TIP2-UDT1, OsUPEX1 and OsUPEX2, predicted to encode galactosyltransferases, that were preferentially expressed in the tapetum. Analysis of their single mutants demonstrated their functional redundancy, while the double knockout mutant revealed their critical roles in tapetum development and function, likely in enabling tapetal secretion.
Overall, this study provides insights into the regulation of rice anther development by TIP2 and UDT1 and identifies downstream targets OsUPEX1 and OsUPEX2 essential for tapetum function and rice male fertility.
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.