Chenchen Wang, Yang Gao, Wen Gong, Thomas Laux, Sha Li, Feng Xiong
{"title":"A tripartite transcriptional module regulates protoderm specification during embryogenesis in Arabidopsis","authors":"Chenchen Wang, Yang Gao, Wen Gong, Thomas Laux, Sha Li, Feng Xiong","doi":"10.1111/nph.20371","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Protoderm formation is a crucial step in early embryo patterning in plants, separating the precursors of the epidermis and the inner tissues. Although key regulators such as ARABIDOPSIS THALIANA MERISTEM LAYER1 (ATML1) and PROTODERMAL FACTOR2 (PDF2) have been identified in the model plant <jats:italic>Arabidopsis thaliana</jats:italic>, the genetic pathways controlling protoderm specification remain largely unexplored.</jats:list-item> <jats:list-item>Here, we combined genetic, cytological, and molecular approaches to investigate the regulatory mechanisms of protoderm specification in <jats:italic>Arabidopsis thaliana</jats:italic>.</jats:list-item> <jats:list-item>We report a novel role of the β‐importin KETCH1 in protoderm specification. <jats:italic>KETCH1</jats:italic> loss‐of‐function leads to aberrant protoderm cell morphology and absent <jats:italic>ATML1</jats:italic> transcription in embryos. We further demonstrate that KETCH1 directly interacts with an RNA Polymerase II (Pol‐II) cofactor JANUS, mediating its nuclear accumulation. Furthermore, JANUS directly interacts with the WUS HOMEOBOX2 (WOX2) protein, which is critical for WOX2‐activated <jats:italic>ATML1</jats:italic> expression. Consequently, <jats:italic>JANUS</jats:italic>, <jats:italic>KETCH1</jats:italic>, and <jats:italic>WOX2</jats:italic> loss‐of‐function results in similar protoderm defects.</jats:list-item> <jats:list-item>Our results identify the tripartite KETCH1/JANUS/WOX2 transcriptional module as a novel regulatory axis in <jats:italic>Arabidopsis</jats:italic> protoderm specification.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"23 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-12-28","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.20371","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
SummaryProtoderm formation is a crucial step in early embryo patterning in plants, separating the precursors of the epidermis and the inner tissues. Although key regulators such as ARABIDOPSIS THALIANA MERISTEM LAYER1 (ATML1) and PROTODERMAL FACTOR2 (PDF2) have been identified in the model plant Arabidopsis thaliana, the genetic pathways controlling protoderm specification remain largely unexplored.Here, we combined genetic, cytological, and molecular approaches to investigate the regulatory mechanisms of protoderm specification in Arabidopsis thaliana.We report a novel role of the β‐importin KETCH1 in protoderm specification. KETCH1 loss‐of‐function leads to aberrant protoderm cell morphology and absent ATML1 transcription in embryos. We further demonstrate that KETCH1 directly interacts with an RNA Polymerase II (Pol‐II) cofactor JANUS, mediating its nuclear accumulation. Furthermore, JANUS directly interacts with the WUS HOMEOBOX2 (WOX2) protein, which is critical for WOX2‐activated ATML1 expression. Consequently, JANUS, KETCH1, and WOX2 loss‐of‐function results in similar protoderm defects.Our results identify the tripartite KETCH1/JANUS/WOX2 transcriptional module as a novel regulatory axis in Arabidopsis protoderm specification.
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.