Chang C H, Fontes J D, Peterlin M, Flavell R A
Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06510.
J Exp Med. 1994 Oct 1;180(4):1367-74. doi: 10.1084/jem.180.4.1367.
The class II transactivator (CIITA) has been shown to be required for major histocompatibility complex (MHC) class II gene expression in B cells and its deficiency is responsible for a hereditary MHC class II deficiency. Here we show that CIITA is also involved in the inducible expression of class II genes upon interferon gamma (IFN-gamma) treatment. The expression of CIITA is also inducible with IFN-gamma before the induction of MHC class II mRNA. In addition, CIITA mRNA expression does not require new protein synthesis, although new protein synthesis is necessary for the transcription of class II. This suggests that synthesis of new CIITA protein may be essential to induce class II gene expression. We also showed that the JAK1 protein tyrosine kinase activity is required to induce the expression of CIITA upon IFN-gamma stimulation. This finding indicates that CIITA is part of the signaling cascade from the IFN-gamma receptor to the activation of class II genes. In addition, the expression of CIITA is sufficient to activate class II genes in the absence of IFN-gamma stimulation suggesting that CIITA is the major regulatory factor for the inducible expression of class II genes. Together, these data suggest that CIITA is the IFN-inducible cycloheximide sensitive factor previously shown to be required for the induction of MHC class II gene expression.
II类反式激活因子(CIITA)已被证明是B细胞中主要组织相容性复合体(MHC)II类基因表达所必需的,其缺陷导致遗传性MHC II类缺陷。在此我们表明,CIITA也参与了γ干扰素(IFN-γ)处理后II类基因的诱导性表达。在MHC II类mRNA诱导之前,CIITA的表达也可被IFN-γ诱导。此外,CIITA mRNA的表达不需要新的蛋白质合成,尽管新的蛋白质合成对于II类基因的转录是必需的。这表明新CIITA蛋白的合成对于诱导II类基因表达可能至关重要。我们还表明,JAK1蛋白酪氨酸激酶活性是IFN-γ刺激后诱导CIITA表达所必需的。这一发现表明,CIITA是从IFN-γ受体到II类基因激活的信号级联反应的一部分。此外,在没有IFN-γ刺激的情况下,CIITA的表达足以激活II类基因,这表明CIITA是II类基因诱导性表达的主要调节因子。总之,这些数据表明,CIITA是先前已证明为诱导MHC II类基因表达所必需的IFN诱导的放线菌酮敏感因子。