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II类反式激活因子与CREB结合蛋白之间的相互作用增强了主要组织相容性复合体II类基因的转录。

Interactions between the class II transactivator and CREB binding protein increase transcription of major histocompatibility complex class II genes.

作者信息

Fontes J D, Kanazawa S, Jean D, Peterlin B M

机构信息

Howard Hughes Medical Institute, Departments of Medicine, Immunology, and Microbiology, University of California San Francisco, San Francisco, California 94143-0703, USA.

出版信息

Mol Cell Biol. 1999 Jan;19(1):941-7. doi: 10.1128/MCB.19.1.941.

Abstract

Class II major histocompatibility (class II) genes are regulated in a B-cell-specific and gamma interferon-inducible fashion. The master switch for the expression of these genes is the class II transactivator (CIITA). In this report, we demonstrate that one of the functions of CIITA is to recruit the CREB binding protein (CBP) to class II promoters. Not only functional but also specific binding interactions between CIITA and CBP were demonstrated. Moreover, a dominant negative form of CBP decreased the activity of class II promoters and levels of class II determinants on the surface of cells. Finally, the inhibition of class II gene expression by the glucocorticoid hormone could be attributed to the squelching of CBP by the glucocorticoid receptor. We conclude that CBP, a histone acetyltransferase, plays an important role in the transcription of class II genes.

摘要

II类主要组织相容性(II类)基因以B细胞特异性和γ干扰素诱导的方式受到调控。这些基因表达的主控开关是II类反式激活因子(CIITA)。在本报告中,我们证明CIITA的功能之一是将CREB结合蛋白(CBP)募集到II类启动子上。不仅证明了CIITA与CBP之间存在功能性且特异性的结合相互作用。此外,CBP的显性负性形式降低了II类启动子的活性以及细胞表面II类决定簇的水平。最后,糖皮质激素对II类基因表达的抑制作用可归因于糖皮质激素受体对CBP的抑制。我们得出结论,作为组蛋白乙酰转移酶的CBP在II类基因的转录中起重要作用。

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