Regulation of gene-activation pathways by pias proteins in the immune system

被引:358
作者
Shuai, K
Liu, B
机构
[1] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nri1667
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The protein inhibitor of activated STAT (PIAS) family of proteins has been proposed to regulate the activity of many transcription factors, including signal transducer and activator of transcription proteins (STATs), nuclear factor-kappa B, SMA- and MAD-related proteins (SMADs), and the tumour-suppressor protein p53. PIAS proteins regulate transcription through several mechanisms, including blocking the DNA-binding activity of transcription factors, recruiting transcriptional corepressors or co-activators, and promoting protein sumoylation. Recent genetic studies support an in vivo function for PIAS proteins in the regulation of innate immune responses. In this article, we review the current understanding of the molecular basis, specificity and physiological roles of PIAS proteins in the regulation of gene-activation pathways in the immune system.
引用
收藏
页码:593 / 605
页数:13
相关论文
共 108 条
[1]   Signalling pathways of the TNF superfamily: A double-edged sword [J].
Aggarwal, BB .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :745-756
[2]   SAP - a putative DNA-binding motif involved in chromosomal organization [J].
Aravind, L ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :112-114
[3]   PIASx is a transcriptional co-repressor of signal transducer and activator of transcription 4 [J].
Arora, T ;
Liu, B ;
He, HC ;
Kim, J ;
Murphy, TL ;
Murphy, KM ;
Modlin, RL ;
Shuai, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (24) :21327-21330
[4]   Smads as transcriptional co-modulators [J].
Attisano, L ;
Wrana, JL .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) :235-243
[5]   A Drosophila PIAS homologue negatively regulates stat92E [J].
Betz, A ;
Lampen, N ;
Martinek, S ;
Young, MW ;
Darnell, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9563-9568
[6]   The two NF-κB activation pathways and their role in innate and adaptive immunity [J].
Bonizzi, G ;
Karin, M .
TRENDS IN IMMUNOLOGY, 2004, 25 (06) :280-288
[7]   Post-translational modification of Rta of Epstein-Barr virus by SUMO-1 [J].
Chang, LK ;
Lee, YH ;
Cheng, TS ;
Hong, YR ;
Lu, PJ ;
Wang, JJ ;
Wang, WH ;
Kuo, CW ;
Li, SSL ;
Liu, ST .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (37) :38803-38812
[8]   Protein partners of C/EBPε [J].
Chih, DY ;
Park, DJ ;
Gross, M ;
Idos, G ;
Vuong, PT ;
Hirama, T ;
Chumakov, AA ;
Said, J ;
Koeffler, HP .
EXPERIMENTAL HEMATOLOGY, 2004, 32 (12) :1173-1181
[9]   Modulation of mRNA expression of a novel human myeloid-selective CCAAT/Enhancer binding protein gene (C/EBP epsilon) [J].
Chih, DY ;
Chumakov, AM ;
Park, DJ ;
Silla, AG ;
Koeffler, HP .
BLOOD, 1997, 90 (08) :2987-2994
[10]   Specific inhibition of Stat3 signal transduction by PIAS3 [J].
Chung, CD ;
Liao, JY ;
Liu, B ;
Rao, XP ;
Jay, P ;
Berta, P ;
Shuai, K .
SCIENCE, 1997, 278 (5344) :1803-1805