Mudhasani Rajini, Fontes Joseph D
Department of Biological, Geological and Environmental Sciences, Cleveland State University, 2399 Euclid Avenue, Cleveland, OH 44115, USA.
Mol Cell Biol. 2002 Jul;22(14):5019-26. doi: 10.1128/MCB.22.14.5019-5026.2002.
The class II transactivator (CIITA) is the key regulator of major histocompatibility complex (MHC) class II gene transcription. We demonstrate here that CIITA requires the ATPase subunit of an hSWI/SNF complex, brahma-related gene 1 (BRG-1), to activate transcription. When introduced into a cell line lacking BRG-1, CIITA was unable to activate cellular MHC class II genes. Reexpression of the wild-type but not an ATP-binding-deficient BRG-1 protein in this cell line restored the ability of CIITA to transactivate transcription of MHC class II genes. Interestingly, when the activity of CIITA was assayed in the BRG-1-deficient cell line by using a plasmid-based reporter assay, BRG-1 was not required for transcriptional activation, suggesting that the chromatin structure on the plasmid is such that BRG-1 is not necessary. Coimmunoprecipitation experiments were performed to determine if BRG-1 and CIITA proteins associate with each other in cells. We found that the two proteins coimmunoprecipitate and that amino acids 1 to 140 of CIITA are sufficient for binding. Taken together, these data suggest that BRG-1 and, very likely, an hSWI/SNF complex are required for transcription of MHC class II genes. The complex is likely recruited to MHC class II promoters, at least in part, by interaction with CIITA.
II类反式激活因子(CIITA)是主要组织相容性复合体(MHC)II类基因转录的关键调节因子。我们在此证明,CIITA需要hSWI/SNF复合体的ATP酶亚基,即与婆罗门相关的基因1(BRG-1)来激活转录。当导入缺乏BRG-1的细胞系时,CIITA无法激活细胞内的MHC II类基因。在此细胞系中重新表达野生型而非ATP结合缺陷型的BRG-1蛋白,可恢复CIITA反式激活MHC II类基因转录的能力。有趣的是,当通过基于质粒的报告基因检测在缺乏BRG-1的细胞系中检测CIITA的活性时,转录激活并不需要BRG-1,这表明质粒上的染色质结构使得BRG-1并非必需。进行了共免疫沉淀实验以确定BRG-1和CIITA蛋白在细胞中是否相互结合。我们发现这两种蛋白可进行共免疫沉淀,且CIITA的第1至140个氨基酸足以实现结合。综上所述,这些数据表明BRG-1以及极有可能的hSWI/SNF复合体是MHC II类基因转录所必需的。该复合体可能至少部分地通过与CIITA相互作用而被招募至MHC II类启动子。