A novel nuclear receptor corepressor complex, N-CoR, contains components of the mammalian SWI/SNF complex and the corepressor KAP-1

被引:242
作者
Underhill, C
Qutob, MS
Yee, SP
Torchia, J
机构
[1] Univ Western Ontario, Canc Res Labs, London Reg Canc Ctr, Dept Pharmacol & Toxicol, London, ON N6A 4L6, Canada
[2] Univ Western Ontario, Canc Res Labs, London Reg Canc Ctr, Dept Oncol, London, ON N6A 4L6, Canada
[3] Univ Western Ontario, Canc Res Labs, London Reg Canc Ctr, Dept Biochem, London, ON N6A 4L6, Canada
关键词
D O I
10.1074/jbc.M007864200
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
Transcriptional silencing by many transcription factors is mediated by the nuclear receptor corepressor (N-CoR). The mechanism by which N-CoR represses basal transcription involves the direct or indirect recruitment of histone deacetylases (HDACs). We have isolated two multiprotein N-CoR complexes, designated N-CoR-1 and N-CoR-2, which possess histone deacetylase activity that is mediated by distinct HDACs. Based on Western blotting using antibodies against known subunits, the only HDAC found in the N-CoR-1 complex was HDAC3. In contrast, N-CoR-2 contained predominantly HDAC1 and HDAC2 as well as several other subunits that are found in the Sin3A HDAC complex. Using mass spectrometry and Western blotting, we have identified several novel components of the N-CoR-1 complex including the SWI/SNF-related proteins BRG1, BAF 170, BAF 155, BAF 47/INI1, and the corepressor KAP-1 that is involved in silencing heterochromatin. Indirect immunofluorescence has revealed that both KAP-1 and N-CoR colocalize throughout the nucleus. These results suggest that N-CoR is found in distinct multiprotein complexes, which are involved in multiple pathways of transcriptional repression.
引用
收藏
页码:40463 / 40470
页数:8
相关论文
共 60 条
[1]   HDA1 and HDA3 are components of a yeast histone deacetylase (HDA) complex [J].
Carmen, AA ;
Rundlett, SE ;
Grunstein, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (26) :15837-15844
[2]   A TRANSCRIPTIONAL CO-REPRESSOR THAT INTERACTS WITH NUCLEAR HORMONE RECEPTORS [J].
CHEN, JD ;
EVANS, RM .
NATURE, 1995, 377 (6548) :454-457
[3]   Nuclear receptors: coactivators, corepressors and chromatin remodeling in the control of transcription [J].
Collingwood, TN ;
Urnov, FD ;
Wolffe, AP .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1999, 23 (03) :255-275
[4]   STIMULATION OF GAL4 DERIVATIVE BINDING TO NUCLEOSOMAL DNA BY THE YEAST SWI/SNF COMPLEX [J].
COTE, J ;
QUINN, J ;
WORKMAN, JL ;
PETERSON, CL .
SCIENCE, 1994, 265 (5168) :53-60
[5]  
Das BK, 1999, MOL CELL BIOL, V19, P6796
[6]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[7]   KAP-1, a novel corepressor for the highly conserved KRAB repression domain [J].
Friedman, JR ;
Fredericks, WJ ;
Jensen, DE ;
Speicher, DW ;
Huang, XP ;
Neilson, EG ;
Rauscher, FJ .
GENES & DEVELOPMENT, 1996, 10 (16) :2067-2078
[8]   Chromatin remodelling by the glucocorticoid receptor requires the BRG1 complex [J].
Fryer, CJ ;
Archer, TK .
NATURE, 1998, 393 (6680) :88-91
[9]  
Glass CK, 2000, GENE DEV, V14, P121
[10]   Fusion proteins of the retinoic acid receptor-α recruit histone deacetylase in promyelocytic leukaemia [J].
Grignani, F ;
De Matteis, S ;
Nervi, C ;
Tomassoni, L ;
Gelmetti, V ;
Cioce, M ;
Fanelli, M ;
Ruthardt, M ;
Ferrara, FF ;
Zamir, I ;
Seiser, C ;
Grignani, F ;
Lazar, MA ;
Minucci, S ;
Pelicci, PG .
NATURE, 1998, 391 (6669) :815-818