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19S ATPase S6a(S6'/TBP1)调节 II 类转录激活因子的转录起始。

The 19S ATPase S6a (S6'/TBP1) regulates the transcription initiation of class II transactivator.

机构信息

Division of Cellular and Molecular Biology and Physiology, Department of Biology, College of Arts and Sciences, Georgia State University, Atlanta, GA 30302, USA.

出版信息

J Mol Biol. 2010 Jan 15;395(2):254-69. doi: 10.1016/j.jmb.2009.10.035. Epub 2009 Oct 21.

Abstract

Class II transactivator (CIITA) is the master regulator of the major histocompatibility class II transcription complex (MHC-II) and is critical for initiation of adaptive immune responses. We have previously demonstrated that the 19S proteasome ATPase Sug1 plays a significant role in regulating CIITA activity and MHC-II expression. We now show that an additional component of the 19S complex, the 19S ATPase S6a (S6'/Tat-binding protein 1), is crucial for regulating cytokine-inducible transcription of CIITA. Lack of S6a negatively impacts CIITA activity and CIITA expression. Decreased expression of S6a significantly diminishes the recruitment of transcription factors to the CIITA interferon-gamma-inducible promoter [CIITA promoter IV (pIV)] and significantly decreases CIITApIV histone H3 and histone H4 acetylation, with a preferential loss of acetylation at H3 lysine 18 and H4 lysine 8. In addition, we provide evidence for the involvement of the 19S AAA (ATPases associated with diverse cellular activity) ATPase hexamer as the 19S ATPase S6b binds CIITApIV in an S6a-dependent fashion and has effects similar to S6a on CIITApIV histone acetylation. These analyses demonstrate the importance of 19S ATPases in the assembly of CIITApIV transcription machinery and provide additional insight into the regulatory mechanisms of the 19S proteasome in mammalian transcription.

摘要

II 类转录激活因子(CIITA)是主要组织相容性复合体 II 转录复合物(MHC-II)的主调控因子,对启动适应性免疫反应至关重要。我们之前已经证明,19S 蛋白酶体 ATP 酶 Sug1 在调节 CIITA 活性和 MHC-II 表达方面发挥着重要作用。现在我们发现,19S 复合物的另一个组成部分,19S ATP 酶 S6a(S6'/Tat 结合蛋白 1),对于调节 CIITA 的细胞因子诱导转录至关重要。S6a 的缺乏会对 CIITA 活性和 CIITA 表达产生负面影响。S6a 表达水平的降低显著减少了转录因子向 CIITA 干扰素-γ诱导启动子 [CIITA 启动子 IV(pIV)] 的募集,并显著降低了 CIITApIV 组蛋白 H3 和组蛋白 H4 的乙酰化,其中 H3 赖氨酸 18 和 H4 赖氨酸 8 的乙酰化优先丢失。此外,我们提供的证据表明,19S AAA(与多种细胞活动相关的 ATP 酶)ATP 酶六聚体参与其中,因为 S6b 以 S6a 依赖的方式结合 CIITApIV,并对 CIITApIV 组蛋白乙酰化产生类似于 S6a 的影响。这些分析表明 19S ATP 酶在 CIITApIV 转录机器的组装中的重要性,并为哺乳动物转录中 19S 蛋白酶体的调节机制提供了更多的见解。

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