Kretsovali A, Agalioti T, Spilianakis C, Tzortzakaki E, Merika M, Papamatheakis J
Department of Biology, University of Crete, Heraklion, Crete, Greece.
Mol Cell Biol. 1998 Nov;18(11):6777-83. doi: 10.1128/MCB.18.11.6777.
The class II transactivator (CIITA) is a key regulatory factor that controls expression of the major histocompatibility complex (MHC) class II genes that are essential components for antigen presentation and thus regulation of the immune response. We show here that the adenovirus E1A protein interferes with the action of CIITA and inhibits both B-cell-specific and gamma interferon (IFN-gamma)-induced expression of MHC class II promoters. Transfection studies provide evidence for the functional role of the CREB-binding protein (CBP) in IFN-gamma and CIITA-mediated MHC class II promoter activation. We demonstrate that the N-terminally located transcription activation domain of CIITA physically interacts with both the N-terminal and the E1A-binding (C/H3) regions of CBP. These results suggest the involvement of a multisubunit complex, which contains the gene-specific coactivator CIITA and the versatile coactivator CBP, in MHC class II gene regulation, which may be responsible for both high-level expression and modulation by different signaling pathways.
II类反式激活因子(CIITA)是一种关键调控因子,可控制主要组织相容性复合体(MHC)II类基因的表达,这些基因是抗原呈递以及免疫反应调控的重要组成部分。我们在此表明,腺病毒E1A蛋白干扰CIITA的作用,并抑制B细胞特异性和γ干扰素(IFN-γ)诱导的MHC II类启动子的表达。转染研究为CREB结合蛋白(CBP)在IFN-γ和CIITA介导的MHC II类启动子激活中的功能作用提供了证据。我们证明,CIITA位于N端的转录激活结构域与CBP的N端和E1A结合(C/H3)区域发生物理相互作用。这些结果表明,一种多亚基复合物参与了MHC II类基因调控过程,该复合物包含基因特异性辅激活因子CIITA和通用辅激活因子CBP,这可能是不同信号通路实现高水平表达和调节的原因。