論文

査読有り
2008年1月

Cell-specific epigenetic regulation of ChM-I gene expression: Crosstalk between DNA methylation and histone acetylation

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  • Tomoki Aoyama
  • Takeshi Okamoto
  • Yoshiki Kohno
  • Kenichi Fukiage
  • Seiji Otsuka
  • Moritoshi Furu
  • Kinya Ito
  • Yonghui Jin
  • Satoshi Nagayama
  • Tomitaka Nakayama
  • Takashi Nakamura
  • Junya Toguchida
  • 全て表示

365
1
開始ページ
124
終了ページ
130
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bbrc.2007.10.135
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

The expression of the chondromodulin-I (ChM-I) gene, a cartilage-specific gene, is regulated by the binding of Sp3 to the core promoter region, which is inhibited by the methylation of CpG in the target genome in the osteogenic lineage, osteosarcoma (OS) cells. The histone tails associated with the hypermethylated promoter region of the ChM-I gene were deacetylated by histone deacetylase 2 (HDAC2) in three ChM-I-negative OS cell lines. Treatment with an HDAC inhibitor induced the binding of Sp3 in one cell line, which became ChM-I-positive. This process was associated with acetylation instead of the dimethylation of historic H3 at lysine 9 (H3-K9) and, surprisingly, the demethylation of the core promoter region. The demethylation was transient, and gradually replaced by methylation after a rapid recovery of histone deacetylaion. These results represent an example of the plasticity of differentiation being regulated by the cell-specific plasticity of epigenetic regulation. (c) 2007 Elsevier Inc. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.bbrc.2007.10.135
J-GLOBAL
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=200902276209453263
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/17980151
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000251493900020&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.bbrc.2007.10.135
  • ISSN : 0006-291X
  • J-Global ID : 200902276209453263
  • PubMed ID : 17980151
  • Web of Science ID : WOS:000251493900020

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