{"title":"The transcription factor DAL1 links age to reproductive development via regulation of LEAFY homologs in conifers","authors":"Yi-Tong Song, Shuang-Wei Liu, Jing-Jing Ma, Xi Chen, Feng-Yi Li, Pei-Yi Wang, Fang-Xu Han, Shi-Hui Niu","doi":"10.1093/plphys/kiaf139","DOIUrl":null,"url":null,"abstract":"Age-dependent reproductive development is pivotal for plant adaptability and for species perpetuation. While substantial progress has been made in elucidating age-related regulatory mechanisms in angiosperms, the molecular basis of how aging pathway interacts with reproductive development in gymnosperms, particularly conifers, remains elusive. Here, we demonstrate that DEFICIENS-AGAMOUS-LIKE 1 (DAL1), an age marker protein in conifers, binds to and activates two LEAFY (LFY) homologs, PtLEAFY (PtLFY) and PtNEEDLY (PtNLY), in Pinus tabuliformis. Furthermore, PtLFY and PtNLY directly regulate class B and C MADS-box genes, which are essential for specifying reproductive organ identity. Notably, PtLFY exerts a stronger regulatory effect on downstream class B and C genes compared to PtNLY, suggesting potential functional divergence between these two paralogous genes. This study reveals a PtDAL1-mediated regulatory cascade that links aging to reproductive development in conifers. These findings provide insights into the evolutionary conservation and divergence of the reproduction-associated regulatory networks across plant lineages, broadening our understanding of the genetic and molecular mechanisms underlying the reproductive development of gymnosperms.","PeriodicalId":20101,"journal":{"name":"Plant Physiology","volume":"21 1","pages":""},"PeriodicalIF":6.9000,"publicationDate":"2025-04-10","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/kiaf139","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
Age-dependent reproductive development is pivotal for plant adaptability and for species perpetuation. While substantial progress has been made in elucidating age-related regulatory mechanisms in angiosperms, the molecular basis of how aging pathway interacts with reproductive development in gymnosperms, particularly conifers, remains elusive. Here, we demonstrate that DEFICIENS-AGAMOUS-LIKE 1 (DAL1), an age marker protein in conifers, binds to and activates two LEAFY (LFY) homologs, PtLEAFY (PtLFY) and PtNEEDLY (PtNLY), in Pinus tabuliformis. Furthermore, PtLFY and PtNLY directly regulate class B and C MADS-box genes, which are essential for specifying reproductive organ identity. Notably, PtLFY exerts a stronger regulatory effect on downstream class B and C genes compared to PtNLY, suggesting potential functional divergence between these two paralogous genes. This study reveals a PtDAL1-mediated regulatory cascade that links aging to reproductive development in conifers. These findings provide insights into the evolutionary conservation and divergence of the reproduction-associated regulatory networks across plant lineages, broadening our understanding of the genetic and molecular mechanisms underlying the reproductive development of gymnosperms.
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.