A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression

被引:1067
作者
Heinzel, T
Lavinsky, RM
Mullen, TM
Soderstrom, M
Laherty, CD
Torchia, J
Yang, WM
Brard, G
Ngo, SD
Davie, JR
Seto, E
Eisenman, RN
Rose, DW
Glass, CK
Rosenfeld, MG
机构
[1] UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, LA JOLLA, CA 92093 USA
[2] UNIV CALIF SAN DIEGO, GRAD PROGRAM BIOL, LA JOLLA, CA 92093 USA
[3] UNIV CALIF SAN DIEGO, WHITTIER DIABET PROGRAM, LA JOLLA, CA 92093 USA
[4] UNIV CALIF SAN DIEGO, CELLULAR & MOL MED DEPT, LA JOLLA, CA 92093 USA
[5] UNIV CALIF SAN DIEGO, SCH MED, LA JOLLA, CA 92093 USA
[6] FRED HUTCHINSON CANC RES CTR, DIV BASIC SCI, SEATTLE, WA 98104 USA
[7] UNIV S FLORIDA, DEPT MED MICROBIOL & IMMUNOL, H LEE MOFFIT CANC CTR & RES INST, TAMPA, FL 33612 USA
[8] UNIV MANITOBA, DEPT BIOCHEM & MOL BIOL, WINNIPEG, MB R3E 0W3, CANADA
关键词
D O I
10.1038/387043a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcriptional repression by nuclear receptors has been correlated to binding of the putative co-repressor, N-CoR, A complex has been identified that contains N-CoR, the Mad presumptive co-repressor mSin3, and the histone deacetylase mRPD3, and which is required for both nuclear receptor- and Mad-dependent repression, but not for repression by transcription factors of the ets-domain family, These data predict that the ligand-induced switch of heterodimeric nuclear receptors from repressor to activator functions involves the exchange of complexes containing histone deacetylases with those that have histone acetylase activity.
引用
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页码:43 / 48
页数:6
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