The emerging role of class II histone deacetylases

被引:160
作者
Fischle, W [1 ]
Kiermer, V [1 ]
Dequiedt, F [1 ]
Verdin, E [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94141 USA
关键词
transcriptional regulation; histone deacetylases; class IIHDACs; nucleocytoplasmic shuttling; MEF2;
D O I
10.1139/bcb-79-3-337
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Histone acetylation and deacetylation play essential roles in modifying chromatin structure and regulating gene expression in all eukaryotes. Several histone acetyltransferases have been identified that act as transcriptional coactivators. In contrast, histone deacetylases (HDACs) are part of transcriptional corepressor complexes. Based on their similarity to known yeast factors, the human HDACs are grouped into three classes. Class I HDACs are similar to the yeast transcriptional repressor yRPD3, while class II HDACs are related 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 in cell differentiation and development, and many molecular details are emerging that shed light on class II HDAC function and regulation. We discuss the biological role of these factors in the context of physiological processes.
引用
收藏
页码:337 / 348
页数:12
相关论文
共 122 条
[11]
Acetylation and chromosomal functions [J].
Cheung, WL ;
Briggs, SD ;
Allis, CD .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (03) :326-333
[12]
Calmodulin: a prototypical calcium sensor [J].
Chin, D ;
Means, AR .
TRENDS IN CELL BIOLOGY, 2000, 10 (08) :322-328
[13]
14-3-3-PROTEINS ASSOCIATE WITH CDC25-PHOSPHATASES [J].
CONKLIN, DS ;
GALAKTIONOV, K ;
BEACH, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7892-7896
[14]
Cress WD, 2000, J CELL PHYSIOL, V184, P1, DOI 10.1002/(SICI)1097-4652(200007)184:1<1::AID-JCP1>3.0.CO
[15]
2-7
[16]
Differential display cloning of a novel human histone deacetylase (HDAC3) cDNA from PHA-activated immune cells [J].
Dangond, F ;
Hafler, DA ;
Tong, JK ;
Randall, J ;
Kojima, R ;
Utku, N ;
Gullans, SR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 242 (03) :648-652
[17]
Davie JR, 1999, J CELL BIOCHEM, P141
[18]
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
[19]
Characterization of a human RPD3 ortholog, HDAC3 [J].
Emiliani, S ;
Fischle, W ;
Van Lint, C ;
Al-Abed, Y ;
Verdin, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2795-2800
[20]
A new family of human histone deacetylases related to Saccharomyces cerevisiae HDA1p [J].
Fischle, W ;
Emiliani, S ;
Hendzel, MJ ;
Nagase, T ;
Nomura, N ;
Voelter, W ;
Verdin, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :11713-11720