論文

査読有り
2016年6月

Auxin-dependent compositional change in Mediator in ARF7-and ARF19-mediated transcription

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
  • Jun Ito
  • ,
  • Hidehiro Fukaki
  • ,
  • Makoto Onoda
  • ,
  • Lin Li
  • ,
  • Chuanyou Li
  • ,
  • Masao Tasaka
  • ,
  • Masahiko Furutani

113
23
開始ページ
6562
終了ページ
6567
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1073/pnas.1600739113
出版者・発行元
NATL ACAD SCIENCES

Mediator is a multiprotein complex that integrates the signals from transcription factors binding to the promoter and transmits them to achieve gene transcription. The subunits of Mediator complex reside in four modules: the head, middle, tail, and dissociable CDK8 kinase module (CKM). The head, middle, and tail modules form the core Mediator complex, and the association of CKM can modify the function of Mediator in transcription. Here, we show genetic and biochemical evidence that CKM-associated Mediator transmits auxin-dependent transcriptional repression in lateral root (LR) formation. The AUXIN/INDOLE 3-ACETIC ACID 14 (Aux/IAA14) transcriptional repressor inhibits the transcriptional activity of its binding partners AUXIN RESPONSE FACTOR 7 (ARF7) and ARF19 by making a complex with the CKM-associated Mediator. In addition, TOPLESS (TPL), a transcriptional corepressor, forms a bridge between IAA14 and the CKM component MED13 through the physical interaction. ChIP assays show that auxin induces the dissociation of MED13 but not the tail module component MED25 from the ARF7 binding region upstream of its target gene. These findings indicate that auxin-induced degradation of IAA14 changes the module composition of Mediator interacting with ARF7 and ARF19 in the upstream region of their target genes involved in LR formation. We suggest that this regulation leads to a quick switch of signal transmission from ARFs to target gene expression in response to auxin.

リンク情報
DOI
https://doi.org/10.1073/pnas.1600739113
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/27217573
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000377155400059&DestApp=WOS_CPL
ID情報
  • DOI : 10.1073/pnas.1600739113
  • ISSN : 0027-8424
  • PubMed ID : 27217573
  • Web of Science ID : WOS:000377155400059

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