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G1B和G3A干扰素γ突变体的分子分析表明,CIITA或RFX的缺陷会导致II类主要组织相容性复合体和Ii基因诱导缺陷。

Molecular analysis of G1B and G3A IFN gamma mutants reveals that defects in CIITA or RFX result in defective class II MHC and Ii gene induction.

作者信息

Chin K C, Mao C, Skinner C, Riley J L, Wright K L, Moreno C S, Stark G R, Boss J M, Ting J P

机构信息

Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill 27599-7260, USA.

出版信息

Immunity. 1994 Nov;1(8):687-97. doi: 10.1016/1074-7613(94)90039-6.

Abstract

Class II major histocompatibility complex (MHC) genes and the invariant (Ii) gene are inducible by interferon-gamma (IFN gamma) but not by interferon-alpha and interferon-beta. The promoter regions of these genes contain three regulatory elements that mediate constitutive and IFN gamma-induced expressions; however, none of the DNA-binding proteins that interact with these elements are regulated by IFN gamma. Recently, a gene coding for a transactivator (CIITA) of class II MHC genes that complements a HLA-DR-negative immunodeficiency has been isolated. Using one IFN gamma mutant cell line (G3A) that is selectively defective in HLA-DR and Ii induction, four lines of evidence are presented to show that CIITA mediates the IFN gamma induction of HLA-DR and Ii genes. Analysis of another mutant line, G1B, indicates that the lack of DRA and Ii gene induction by IFN gamma is correlated with the lack of RFX DNA binding activity, thus providing the link between RFX and an IFN gamma response.

摘要

II类主要组织相容性复合体(MHC)基因和恒定链(Ii)基因可被γ干扰素(IFNγ)诱导,但不能被α干扰素和β干扰素诱导。这些基因的启动子区域包含三个调节元件,介导组成型和IFNγ诱导的表达;然而,与这些元件相互作用的DNA结合蛋白均不受IFNγ调节。最近,已分离出一种编码II类MHC基因反式激活因子(CIITA)的基因,该基因可弥补HLA-DR阴性免疫缺陷。利用一种在HLA-DR和Ii诱导方面存在选择性缺陷的IFNγ突变细胞系(G3A),提供了四条证据表明CIITA介导IFNγ对HLA-DR和Ii基因的诱导。对另一个突变系G1B的分析表明,IFNγ缺乏对DRA和Ii基因的诱导与缺乏RFX DNA结合活性相关,从而在RFX与IFNγ反应之间建立了联系。

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