{"title":"Phylostratigraphic analysis revealed that ancient ohnologue PtoWRKY53 innovated a vascular transcription regulatory network in Populus.","authors":"Weixiong Huang,Mingyang Quan,Weina Qi,Liang Xiao,Yuanyuan Fang,Jiaxuan Zhou,Tailin Ren,Peng Li,Yongming Chen,Yousry A El-Kassaby,Fang Du,Deqiang Zhang","doi":"10.1111/nph.70403","DOIUrl":null,"url":null,"abstract":"The secondary vascular system represents a hallmark innovation in woody plant evolution. While contemporary studies have decoded key molecular networks governing its development, the evolutionary trajectory of these regulatory systems remains elusive. We performed integrated phylostratigraphic and transcriptomic profiling across six Populus species spanning five phylogenetic clades to decipher the evolutionary dynamics of regulatory genes in the secondary vascular system. This analysis revealed that over 51% of regulatory genes originated from the most ancient phylostratum (PS1). The observed 65% gene expansion in the PS1 was driven by whole-genome duplication (WGD). Through phylotranscriptomic and gene co-expression network analysis, we found that dosage-unconstrained ohnologues from three PS1 families, MYB domain protein, NAC domain containing protein, and WRKY DNA-binding protein, have significant xylem-specific expression. We identified an ohnologue, PtoWRKY53, which forms a new transcription regulatory network in xylem via neofunctionalization. Transgenic analyses revealed that PtoWRKY53 transcriptionally represses PtoCESA3, thereby inhibiting xylem secondary wall biosynthesis and reducing poplar height (26.39%) and stem diameter (18.36%). Our study highlights the importance of interactions between ancient genes and WGD in generating morphological innovations of the secondary vasculature in Populus.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"26 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-07-21","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.70403","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 secondary vascular system represents a hallmark innovation in woody plant evolution. While contemporary studies have decoded key molecular networks governing its development, the evolutionary trajectory of these regulatory systems remains elusive. We performed integrated phylostratigraphic and transcriptomic profiling across six Populus species spanning five phylogenetic clades to decipher the evolutionary dynamics of regulatory genes in the secondary vascular system. This analysis revealed that over 51% of regulatory genes originated from the most ancient phylostratum (PS1). The observed 65% gene expansion in the PS1 was driven by whole-genome duplication (WGD). Through phylotranscriptomic and gene co-expression network analysis, we found that dosage-unconstrained ohnologues from three PS1 families, MYB domain protein, NAC domain containing protein, and WRKY DNA-binding protein, have significant xylem-specific expression. We identified an ohnologue, PtoWRKY53, which forms a new transcription regulatory network in xylem via neofunctionalization. Transgenic analyses revealed that PtoWRKY53 transcriptionally represses PtoCESA3, thereby inhibiting xylem secondary wall biosynthesis and reducing poplar height (26.39%) and stem diameter (18.36%). Our study highlights the importance of interactions between ancient genes and WGD in generating morphological innovations of the secondary vasculature in Populus.
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.