Sin3: a flexible regulator of global gene expression and genome stability

被引:258
作者
Silverstein, RA [1 ]
Ekwall, K [1 ]
机构
[1] Univ Coll Sodertorn, Karolinska Inst, Dept Biosci, S-14189 Huddinge, Sweden
关键词
SIN3; histone acetylation; chromatin; gene regulation; corepressor;
D O I
10.1007/s00294-004-0541-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
SIN3 was first identified genetically as a global regulator of transcription. Sin3 is a large protein composed mainly of protein-interaction domains, whose function is to provide structural support for a heterogeneous Sin3/histone deacetylase (HDAC) complex. The core Sin3/HDAC complex is conserved from yeast to man and consists of eight proteins. In addition to HDACs, Sin3 can sequester other enzymatic functions, including nucleosome remodeling, DNA methylation, N-acetylglucoseamine transferase activity, and histone methylation. Since the Sin3/HDAC complex lacks any DNA-binding activity, it must be targeted to gene promoters by interacting with DNA-binding proteins. Although most research on Sin3 has focused on its role as a corepressor, mounting evidence suggests that Sin3 can also positively regulate transcription. Furthermore, Sin3 is key to the propagation of epigenetically silenced domains and is required for centromere function. Thus, Sin3 provides a platform to deliver multiple combinations modifications to the chromatin, using both sequence-specific and sequence-independent mechanisms.
引用
收藏
页码:1 / 17
页数:17
相关论文
共 120 条
[1]   Identification of mammalian Sds3 as an integral component of the Sin3/histone deacetylase corepressor complex [J].
Alland, L ;
David, G ;
Hong, SL ;
Potes, J ;
Muhle, R ;
Lee, HC ;
Hou, H ;
Chen, K ;
DePinho, RA .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (08) :2743-2750
[2]   Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression [J].
Alland, L ;
Muhle, R ;
Hou, H ;
Potes, J ;
Chin, L ;
SchreiberAgus, N ;
DePinho, RA .
NATURE, 1997, 387 (6628) :49-55
[3]   The Rpd3-Sin3 histone deacetylase regulates replication timing and enables intra-S origin control in Saccharomyces cerevisiae [J].
Aparicio, JG ;
Viggiani, CJ ;
Gibson, DG ;
Aparicio, OM .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (11) :4769-4780
[4]   MAD-MAX TRANSCRIPTIONAL REPRESSION IS MEDIATED BY TERNARY COMPLEX-FORMATION WITH MAMMALIAN HOMOLOGS OF YEAST REPRESSOR SIN3 [J].
AYER, DE ;
LAWRENCE, QA ;
EISENMAN, RN .
CELL, 1995, 80 (05) :767-776
[5]   The Max network gone mad [J].
Baudino, TA ;
Cleveland, JL .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (03) :691-702
[6]   Genomewide studies of histone deacetylase function in yeast [J].
Bernstein, BE ;
Tong, JK ;
Schreiber, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13708-13713
[7]   BIPARTITE STRUCTURE OF AN EARLY MEIOTIC UPSTREAM ACTIVATION SEQUENCE FROM SACCHAROMYCES-CEREVISIAE [J].
BOWDISH, KS ;
MITCHELL, AP .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2172-2181
[8]   SMRT isoforms mediate repression and anti-repression of nuclear receptor heterodimers [J].
Chen, JD ;
Umesono, K ;
Evans, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (15) :7567-7571
[9]   Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle- and developmentally regulated promoter (Publication with Expression of Concern) [J].
Cosma, MP ;
Tanaka, TU ;
Nasmyth, K .
CELL, 1999, 97 (03) :299-311
[10]  
Dang VD, 1999, MOL CELL BIOL, V19, P2351