T Winkelmolen,P Colleoni,M J Moscou,P Hoseinzadeh,K Oldach,R C Schmidt,R G H Immink,G W van Esse
{"title":"VULGARE ROW-TYPE SIX 5 binds to the promoter of tillering and floral homeotic genes to regulate their expression.","authors":"T Winkelmolen,P Colleoni,M J Moscou,P Hoseinzadeh,K Oldach,R C Schmidt,R G H Immink,G W van Esse","doi":"10.1093/plphys/kiaf309","DOIUrl":null,"url":null,"abstract":"Variation in shoot architecture, or tillering, is an important adaptive trait targeted during the domestication of crops. A well-known regulatory factor in shoot architecture is TEOSINTE BRANCHED 1 (TB1). TB1 and its orthologs have a conserved function in integrating environmental signals to regulate axillary branching or tillering in cereals. The barley (Hordeum vulgare) ortholog of TB1, VULGARE ROW-TYPE SIX 5 (VRS5), regulates tillering and is involved in regulating row-type by inhibiting lateral spikelet development. These discoveries predominantly come from genetic studies; however, how VRS5 regulates these processes on a molecular level remains largely unknown. By combining transcriptome analysis between the vrs5 mutant and the wild type at different developmental stages and DAP-sequencing to locate the genome-wide DNA binding sites of VRS5, we identified bona fide targets of VRS5. We found that VRS5 targets abscisic acid-related genes, potentially to inhibit tillering in a conserved way. Later in inflorescence development, VRS5 also targets row-type gene VRS1 and several known floral development genes, such as MIKCc-type MADS-box genes. This study identifies several genes for mutational analysis, representing a selection of bona fide targets that will contribute to a deeper understanding of the VRS5 network and its role in shaping barley development.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"17 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/plphys/kiaf309","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
Variation in shoot architecture, or tillering, is an important adaptive trait targeted during the domestication of crops. A well-known regulatory factor in shoot architecture is TEOSINTE BRANCHED 1 (TB1). TB1 and its orthologs have a conserved function in integrating environmental signals to regulate axillary branching or tillering in cereals. The barley (Hordeum vulgare) ortholog of TB1, VULGARE ROW-TYPE SIX 5 (VRS5), regulates tillering and is involved in regulating row-type by inhibiting lateral spikelet development. These discoveries predominantly come from genetic studies; however, how VRS5 regulates these processes on a molecular level remains largely unknown. By combining transcriptome analysis between the vrs5 mutant and the wild type at different developmental stages and DAP-sequencing to locate the genome-wide DNA binding sites of VRS5, we identified bona fide targets of VRS5. We found that VRS5 targets abscisic acid-related genes, potentially to inhibit tillering in a conserved way. Later in inflorescence development, VRS5 also targets row-type gene VRS1 and several known floral development genes, such as MIKCc-type MADS-box genes. This study identifies several genes for mutational analysis, representing a selection of bona fide targets that will contribute to a deeper understanding of the VRS5 network and its role in shaping barley development.
期刊介绍:
Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research.
As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.