SAP30, a component of the mSin3 corepressor complex involved in N-CoR-mediated repression by specific transcription factors

被引:184
作者
Laherty, CD
Billin, AN
Lavinsky, RM
Yochum, GS
Bush, AC
Sun, JM
Mullen, TM
Davie, JR
Rose, DW
Glass, CK
Rosenfeld, MG
Ayer, DE
Eisenman, RN
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
[2] Univ Utah, Huntsman Canc Inst, Dept Oncol Sci, Div Mol Biol & Genet, Salt Lake City, UT 84112 USA
[3] Univ Calif San Diego, Dept Med, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Med, Whittier Diabet Program, La Jolla, CA 92093 USA
[5] Univ Manitoba, Dept Biochem & Mol Biol, Winnipeg, MB R3E 0W3, Canada
关键词
D O I
10.1016/S1097-2765(00)80111-2
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
The transcriptional corepressor mSin3 is found in a large multiprotein complex containing the histone deacetylases HDAC1 and HDAC2, in addition to at least five tightly associated polypeptides. We have cloned and characterized a novel component of the mSin3 complex, SAP30. SAP30 binds to mSin3 and is capable of mediating transcriptional repression via histone deacetylases. SAP30 also binds the N-CoR corepressor and is required for N-CoR-mediated repression by antagonist-bound estrogen receptor and the homeodomain protein Rpx, as well as N-CoR suppression of transactivation by the POU domain protein Pit-1. However, SAP30 is not required for N-CoR-mediated repression by unliganded retinoic acid receptor or thyroid hormone receptor, suggesting that SAP30 is involved in the functional recruitment of the mSin3-histone deacetylase complex to a specific subset of N-CoR corepressor complexes.
引用
收藏
页码:33 / 42
页数:10
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