PARP-2 regulates cell cycle-related genes through histone deacetylation and methylation independently of poly(ADP-ribosyl)ation

被引:16
作者
Liang, Ya-Chen [1 ]
Hsu, Chiao-Yu [1 ]
Yao, Ya-Li [2 ]
Yang, Wen-Ming [1 ]
机构
[1] Natl Chung Hsing Univ, Inst Mol Biol, 250 Kuo Kuang Rd, Taichung 40227, Taiwan
[2] Asia Univ, Dept Biotechnol, Taichung 41354, Taiwan
关键词
Poly(ADP-ribosyl)ation; PARP-2; HDAC5; HDAC7; G9a; YY1; c-MYC; CHROMATIN-STRUCTURE; DNA-REPAIR; TRANSCRIPTION; EXPRESSION; BINDING; DIFFERENTIATION; MODULATION; ACTIVATION; REPRESSION; ROLES;
D O I
10.1016/j.bbrc.2012.12.092
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
Poly(ADP-ribose) polymerase-2 (PARP-2) catalyzes poly(ADP-ribosyl)ation (PARylation) and regulate numerous nuclear processes, including transcription. Depletion of PARP-2 alters the activity of transcription factors and global gene expression. However, the molecular action of how PARP-2 controls the transcription of target promoters remains unclear. Here we report that PARP-2 possesses transcriptional repression activity independently of its enzymatic activity. PARP-2 interacts and recruits histone deacetylases HDAC5 and HDAC7, and histone methyltransferase G9a to the promoters of cell cycle-related genes, generating repressive chromatin signatures. Our findings propose a novel mechanism of PARP-2 in transcriptional regulation involving specific protein-protein interactions and highlight the importance of PARP-2 in the regulation of cell cycle progression. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:58 / 64
页数:7
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