Nuclear integration of JAK/STAT and Ras/AP-1 signaling by CBP and p300

被引:374
作者
Horvai, AE
Xu, L
Korzus, E
Brard, G
Kalafus, D
Mullen, TM
Rose, DW
Rosenfeld, MG
Glass, CK
机构
[1] UNIV CALIF SAN DIEGO, DEPT MED, DIV CELLULAR & MOL MED, LA JOLLA, CA 92093 USA
[2] UNIV CALIF SAN DIEGO, DIV ENDOCRINOL & METAB, LA JOLLA, CA 92093 USA
[3] UNIV CALIF SAN DIEGO, HOWARD HUGHES MED INST, LA JOLLA, CA 92093 USA
[4] UNIV CALIF SAN DIEGO, WHITTIER INST, LA JOLLA, CA 92093 USA
关键词
D O I
10.1073/pnas.94.4.1074
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
We report that interferon gamma (IFN-gamma) inhibits transcription of the macrophage scavenger receptor gene by antagonizing the Ras-dependent activities of AP-1 and cooperating ets domain transcription factors, apparently as a result of competition between AP-1/ets factors and activated STAT1 for limiting amounts of CBP and p300. Consistent with this model, STAT1 alpha interacts directly with CBP in cells, and microinjection of anti-CBP and anti-p300 antibodies blocks transcriptional responses to IFN-gamma, Cells lacking STAT1 fail to inhibit AP-1/ets activity, and overexpression of CBP both potentiates IFN-gamma-dependent transcription and relieves AP-1/ets repression, Thus, CBP and p300 integrate both positive and negative effects of IFN-gamma on gene expression by serving as essential coactivators of STAT1 alpha, modulating gene-specific responses to simultaneous activation of two or more signal transduction pathways.
引用
收藏
页码:1074 / 1079
页数:6
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