Combinatorial roles of the nuclear receptor corepressor in transcription and development

被引:421
作者
Jepsen, K
Hermanson, O
Onami, TM
Gleiberman, AS
Lunyak, V
McEvilly, RJ
Kurokawa, R
Kumar, V
Liu, F
Seto, E
Hedrick, SM
Mandel, G
Glass, CK
Rose, DW
Rosenfeld, MG [1 ]
机构
[1] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[4] Univ S Florida, H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[5] SUNY Stony Brook, Howard Hughes Med Inst, Stony Brook, NY 11794 USA
[6] Univ Calif San Diego, Div Endocrinol & Metab, La Jolla, CA 92093 USA
关键词
D O I
10.1016/S0092-8674(00)00064-7
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 repression plays crucial roles in diverse aspects of metazoan development, implying critical regulatory roles for corepressors such as N-CoR and SMRT. Altered patterns of transcription in tissues and cells derived from N-CoR gene-deleted mice and the resulting block at specific points in CNS, erythrocyte, and thymocyte development indicated that N-CoR was a required component of short-term active repression by nuclear receptors and MAD and of a subset of long-term repression events mediated by REST/NRSF. Unexpectedly, N-CoR and a specific deacetylase were also required for transcriptional activation of one class of retinoic acid response element. Together, these findings suggest that specific combinations of corepressors and histone deacetylases mediate the gene-specific actions of DNA-bound repressors in development of multiple organ systems.
引用
收藏
页码:753 / 763
页数:11
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