The transcriptional co-activator p/CIP binds CBP and mediates nuclear-receptor function

被引:1090
作者
Torchia, J
Rose, DW
Inostroza, J
Kamei, Y
Westin, S
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, DEPT MED, 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 SCH, LA JOLLA, CA 92093 USA
关键词
D O I
10.1038/42652
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
The functionally conserved proteins CBP and p300 act in conjunction with other factors to activate transcription of DNA. A new factor, p/CIP, has been discovered that is present in the cell as a complex with CEP and is required for transcriptional activity of nuclear receptors and other CBP/p300-dependent transcription factors. The highly related nuclear-receptor co-activator protein NCoA-1 is also specifically required for ligand-dependent activation of genes by nuclear receptors, p/CIP, NCoA-1 and CBP all contain related leucine-rich charged helical interaction motifs that ape required for receptor-specific mechanisms of gene activation, and allow the selective inhibition of distinct signal-transduction pathways.
引用
收藏
页码:677 / 684
页数:8
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