Morris A C, Spangler W E, Boss J M
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Immunol. 2000 Apr 15;164(8):4143-9. doi: 10.4049/jimmunol.164.8.4143.
Inhibition of class II trans-activator (CIITA) expression prevents embryonic trophoblast cells from up-regulating MHC class II genes in response to IFN-gamma. This is thought to be one mechanism of maternal tolerance to the fetal allograft. The CIITA gene is regulated by four distinct promoters; promoter III directs constitutive (B cell) expression, and promoter IV regulates IFN-gamma-inducible expression. Using in vivo genomic footprinting, promoter-reporter analysis, Southern blot analysis, and RT-PCR, we have examined the cause of CIITA silencing in a trophoblast-derived cell line. We report here that methylation of promoter IV DNA at CpG sites in Jar cells prevents promoter occupancy and IFN-gamma-inducible transcription. The inhibition of CpG methylation in Jar cells by treatment with 5-aza-2'-deoxycytidine restores IFN-gamma inducibility to CIITA. This is the first description of an epigenetic mechanism involved in regulation of CIITA and MHC class II gene expression.
II类反式激活因子(CIITA)表达的抑制可阻止胚胎滋养层细胞响应γ干扰素而上调MHC II类基因。这被认为是母体对胎儿同种异体移植物产生耐受的一种机制。CIITA基因受四个不同启动子调控;启动子III指导组成型(B细胞)表达,启动子IV调节γ干扰素诱导的表达。我们利用体内基因组足迹法、启动子-报告基因分析、Southern印迹分析和逆转录-聚合酶链反应,研究了滋养层来源细胞系中CIITA沉默的原因。我们在此报告,Jar细胞中启动子IV DNA在CpG位点的甲基化阻止了启动子占据和γ干扰素诱导的转录。用5-氮杂-2'-脱氧胞苷处理抑制Jar细胞中的CpG甲基化,可恢复CIITA对γ干扰素的诱导性。这是首次描述参与CIITA和MHC II类基因表达调控的表观遗传机制。