HDAC4, a human histone deacetylase related to yeast HDA1, is a transcriptional corepressor

被引:0
|
作者
Wang, AH
Bertos, NR
Vezmar, M
Pelletier, N
Crosato, M
Heng, HH
Th'ng, J
Han, JH
Yang, XJ
机构
[1] McGill Univ, Dept Med, Mol Oncol Grp, Montreal, PQ, Canada
[2] McGill Univ, Lady Davis Inst Med Res, Montreal, PQ, Canada
[3] York Univ, Dept Biol, N York, ON M3J 1P3, Canada
[4] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
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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
Histone acetylation plays an important role in regulating chromatin structure and thus gene expression. Here we describe the functional characterization of HDAC4, a human histone deacetylase whose C-terminal part displays significant sequence similarity to the deacetylase domain of yeast HDA1. HDAC4 is expressed in various adult human tissues, and its gene is located at chromosome band 2q37. HDAC4 possesses histone deacetylase activity intrinsic to its C-terminal domain. When tethered to a promoter, HDAC4 represses transcription through two independent repression domains, with repression domain 1 consisting of the N-terminal 208 residues and repression domain 2 containing the deacetylase domain. Through a small region located at its N-terminal domain, HDAC4 interacts with the MADS-box transcription factor MEF2C. Furthermore, HDAC4 and MEF2C individually upregulate but together downmodulate c-jun promoter activity. These results suggest that HDAC4 interacts with transcription factors such as MEF2C to negatively regulate gene expression.
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页码:7816 / 7827
页数:12
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