Class II histone deacetylases: versatile regulators

被引:531
作者
Verdin, E [1 ]
Dequiedt, F [1 ]
Kasler, HG [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94141 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0168-9525(03)00073-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Histone acetylation and deacetylation play essential roles in modifying chromatin structure and regulating gene expression in eukaryotes. Histone deacetylases (HDACs) catalyze the deacetylation of lysine residues in the histone N-terminal tails and are found in large multiprotein complexes with transcriptional co-repressors. Human HDACs are grouped into three classes based on their similarity to known yeast factors: class I HDACs are similar to the yeast transcriptional repressor yRPD3, class II HDACs to yHDA1 and class III HDACs to ySIR2. In this review, we focus on the biology of class II HDACs. These newly discovered enzymes have been implicated as global regulators of gene expression during cell differentiation and development. We discuss their emerging biological functions and the molecular mechanisms by which they are regulated.
引用
收藏
页码:286 / 293
页数:8
相关论文
共 89 条
[1]   Nuclear hormone receptors and gene expression [J].
Aranda, A ;
Pascual, A .
PHYSIOLOGICAL REVIEWS, 2001, 81 (03) :1269-1304
[2]   Ca2+-dependent gene expression mediated by MEF2 transcription factors [J].
Blaeser, F ;
Ho, N ;
Prywes, R ;
Chatila, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) :197-209
[3]  
CALNAN BJ, 1995, IMMUNITY, V3, P273
[4]   Acetylation and chromosomal functions [J].
Cheung, WL ;
Briggs, SD ;
Allis, CD .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (03) :326-333
[5]   CtBP, an unconventional transcriptional corepressor in development and oncogenesis [J].
Chinnadurai, G .
MOLECULAR CELL, 2002, 9 (02) :213-224
[6]   SUMO-1 modification of histone deacetylase 1 (HDAC1) modulates its biological activities [J].
David, G ;
Neptune, MA ;
DePinho, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (26) :23658-23663
[7]   Corepressor SMRT binds the BTB/POZ repressing domain of the LAZ3/BCL6 oncoprotein [J].
Dhordain, P ;
Albagli, O ;
Lin, RJ ;
Ansieau, S ;
Quief, S ;
Leutz, A ;
Kerckaert, JP ;
Evans, RM ;
Leprince, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10762-10767
[8]   Identification of a nuclear domain with deacetylase activity [J].
Downes, M ;
Ordentlich, P ;
Kao, HY ;
Alvarez, JGA ;
Evans, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10330-10335
[9]   A dynamic role for HDAC7 in MEF2-mediated muscle differentiation [J].
Dressel, U ;
Bailey, PJ ;
Wang, SCM ;
Downes, M ;
Evans, RM ;
Muscat, GEO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (20) :17007-17013
[10]   Deletion of calcineurin and myocyte enhancer factor 2 (MEF2) binding domain of Cabin1 results in enhanced cytokine gene expression in T cells [J].
Esau, C ;
Boes, M ;
Youn, HD ;
Tatterson, L ;
Liu, JO ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (10) :1449-1459