PIASx is a transcriptional co-repressor of signal transducer and activator of transcription 4

被引:110
作者
Arora, T
Liu, B
He, HC
Kim, J
Murphy, TL
Murphy, KM
Modlin, RL
Shuai, K
机构
[1] Univ Calif Los Angeles, Div Hematol Oncol, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Div Dermatol, Dept Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Div Biol Chem, Los Angeles, CA 90095 USA
[4] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
D O I
10.1074/jbc.C300119200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In response to interleukin 12 ( IL- 12) stimulation, a latent cytoplasmic transcription factor, Stat4 ( signal transducer and activator of transcription 4), becomes tyrosine- phosphorylated and translocates into the nucleus where it binds to DNA to activate transcription. Cofactors that can directly bind and regulate Stat4 activity have not been described. We report here that PI-ASx, a member of the protein inhibitor of activated STAT ( PIAS) family, is a negative regulator of Stat4. PIASx becomes associated with Stat4 following IL- 12 stimulation in vivo. PIASx inhibits IL- 12- stimulated and Stat4- dependent gene activation in human T cells. PIASx does not inhibit the DNA binding activity of Stat4. Instead PIASx is present in the Stat4- DNA binding complex. Finally the inhibitory activity of PIASx on Stat4-mediated gene activation is abolished by the histone deacetylase inhibitor trichostatin A. Our results suggest that PIASx may function as a co- repressor of Stat4.
引用
收藏
页码:21327 / 21330
页数:4
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