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

被引:17
作者
Aoyama, Tomoki [1 ]
Okamoto, Takeshi
Kohno, Yoshiki
Fukiage, Kenichi
Otsuka, Seiji
Furu, Moritoshi
Ito, Kinya
Jin, Yonghui
Nagayama, Satoshi
Nakayama, Tomitaka
Nakamura, Takashi
Toguchida, Junya
机构
[1] Kyoto Univ, Inst Frontier Med Sci, Kyoto, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Orthopaed Surg, Kyoto, Japan
[3] Nagoya City Univ, Grad Sch Med Sci, Dept Musculoskeletal Med, Nagoya, Aichi, Japan
[4] Grad Sch Med, Dept Surg & Surg Basic Sci, Kyoto, Japan
基金
日本学术振兴会;
关键词
chondromodulin-I; histone modification; acetylation; differentiation; epigenetic; chondrogenic; methylation; H3-K9; HDAC2;
D O I
10.1016/j.bbrc.2007.10.135
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:124 / 130
页数:7
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