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干扰素JAK-STAT途径中STAT1和STAT2的转录调控。

Transcriptional regulation by STAT1 and STAT2 in the interferon JAK-STAT pathway.

作者信息

Au-Yeung Nancy, Mandhana Roli, Horvath Curt M

机构信息

Department of Molecular Biosciences; Northwestern University; Evanston, IL USA.

出版信息

JAKSTAT. 2013 Jul 1;2(3):e23931. doi: 10.4161/jkst.23931. Epub 2013 Jun 18.

Abstract

STAT1 and STAT2 proteins are key mediators of type I and type III interferon (IFN) signaling, and are essential components of the cellular antiviral response and adaptive immunity. They associate with IFN regulatory factor 9 (IRF9) to form a heterotrimeric transcription factor complex known as ISGF3. The regulation of IFN-stimulated gene (ISG) expression has served as a model of JAK-STAT signaling and mammalian transcriptional regulation, but to date has primarily been analyzed at the single gene level. While many aspects of ISGF3-mediated gene regulation are thought to be common features applicable to several ISGs, there are also many reports of distinct cases of non-canonical STAT1 or STAT2 signaling events and distinct patterns of co-regulators that contribute to gene-specific transcription. Recent genome-wide studies have begun to uncover a more complete profile of ISG regulation, moving toward a genome-wide understanding of general mechanisms that underlie gene-specific behaviors.

摘要

信号转导和转录激活因子1(STAT1)和信号转导和转录激活因子2(STAT2)蛋白是I型和III型干扰素(IFN)信号传导的关键介质,是细胞抗病毒反应和适应性免疫的重要组成部分。它们与干扰素调节因子9(IRF9)结合,形成一种称为ISGF3的异源三聚体转录因子复合物。干扰素刺激基因(ISG)表达的调控已成为JAK-STAT信号传导和哺乳动物转录调控的模型,但迄今为止主要是在单基因水平上进行分析。虽然ISGF3介导的基因调控的许多方面被认为是适用于多个ISG的共同特征,但也有许多关于非经典STAT1或STAT2信号事件的不同案例以及有助于基因特异性转录的共调节因子的不同模式的报道。最近的全基因组研究已经开始揭示ISG调控的更完整概况,朝着对基因特异性行为背后的一般机制的全基因组理解迈进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77bf/3772101/ddc821d13820/jkst-2-e23931-g1.jpg

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