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YB-1 DNA结合蛋白抑制II类主要组织相容性复合体基因的γ干扰素激活。

YB-1 DNA-binding protein represses interferon gamma activation of class II major histocompatibility complex genes.

作者信息

Ting J P, Painter A, Zeleznik-Le N J, MacDonald G, Moore T M, Brown A, Schwartz B D

机构信息

Department of Microbiology-Immunology, University of North Carolina at Chapel Hill 27599-7295.

出版信息

J Exp Med. 1994 May 1;179(5):1605-11. doi: 10.1084/jem.179.5.1605.

Abstract

Interferon gamma (IFN-gamma) is the most potent inducer of class II major histocompatibility complex (MHC) genes. This induction is uniquely mediated by three DNA elements in the promoter region of class II MHC genes. One of these DNA elements, Y, contains an inverted CCAAT box. Previously, we have screened a lambda gt11 library for Y-binding proteins and identified the YB-1 gene. Here we provide evidence that YB-1 can repress the IFN-gamma induction of class II MHC promoter as well as the Invariant chain (Ii) gene which also contains a Y element in its promoter. This was demonstrated by cotransfecting a YB-1 expression vector with promoter-reporter gene constructs. As an alternate approach, an efficient transient transfection system was developed which resulted in a > 70% transfection efficiency. Transfection of YB-1 by this procedure resulted in the near abrogation of IFN-gamma induced HLA-DR antigen and mRNA expression. These findings show the functional suppression of class II MHC gene induction by the YB-1 protein.

摘要

γ干扰素(IFN-γ)是II类主要组织相容性复合体(MHC)基因最有效的诱导剂。这种诱导作用由II类MHC基因启动子区域的三个DNA元件独特介导。其中一个DNA元件Y含有一个反向CCAAT框。此前,我们已针对与Y结合的蛋白筛选了λgt11文库,并鉴定出YB-1基因。在此我们提供证据表明,YB-1可抑制II类MHC启动子以及恒定链(Ii)基因的IFN-γ诱导,Ii基因启动子中也含有一个Y元件。这是通过将YB-1表达载体与启动子-报告基因构建体共转染来证明的。作为另一种方法,开发了一种高效的瞬时转染系统,其转染效率>70%。通过该程序转染YB-1导致IFN-γ诱导的HLA-DR抗原和mRNA表达几乎完全消除。这些发现表明YB-1蛋白对II类MHC基因诱导具有功能抑制作用。

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