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一种抑制人类主要组织相容性复合体II类基因DPA转录的锌指蛋白。

A zinc finger protein that represses transcription of the human MHC class II gene, DPA.

作者信息

Scholl T, Stevens M B, Mahanta S, Strominger J L

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

J Immunol. 1996 Feb 15;156(4):1448-57.

PMID:8568247
Abstract

The proximal promoters of all MHC class II genes contain a sequence element, the 19-bp X box, that is conserved in both sequence and position. Extensive analysis using a wide variety of approaches has demonstrated that the integrity of the X box is essential for transcription initiation from all class II genes studied. However, the X box is now recognized to contain two subregions, termed X1 and X2. Radiolabeled oligonucleotides corresponding to the X2 box of the MHC class II genes DPA and DQB were used to screen B cell and T cell expression libraries. A novel cDNA, termed XBR (X box repressor), encoding a putative zinc finger protein that binds specifically to the DPA X2 box was isolated from a human T cell line. The XBR gene encodes a 7-kb message that is ubiquitously transcribed, although at higher levels in tissues of the lymphocytic compartment. Southern blots indicate that this gene is single copy in primates and contains regions that are highly divergent in other species. Overexpression of XBR in a B cell line resulted in a dramatic reduction of transcription from a reporter gene construct driven by the DPA promoter, but not from similar constructs with mutations in the X2 box. Similarly, overexpression of XBR reduced induction of reporter gene activity driven from the DPA promoter in HeLa cells treated with IFN-gamma. XBR may, therefore, mediate transcriptional repression, thus preventing inappropriate MHC class II expression. XBR function may in part explain the dominant trans-acting repression of MHC class II expression reported in cell fusion experiments.

摘要

所有MHC II类基因的近端启动子都含有一个序列元件,即19bp的X盒,其序列和位置都是保守的。使用多种方法进行的广泛分析表明,X盒的完整性对于所有研究的II类基因的转录起始至关重要。然而,现在人们认识到X盒包含两个子区域,称为X1和X2。对应于MHC II类基因DPA和DQB的X2盒的放射性标记寡核苷酸被用于筛选B细胞和T细胞表达文库。从人T细胞系中分离出一种新的cDNA,称为XBR(X盒阻遏物),它编码一种假定的锌指蛋白,该蛋白特异性结合DPA X2盒。XBR基因编码一个7kb的信使RNA,它在各处都有转录,尽管在淋巴细胞区室的组织中水平较高。Southern印迹表明,该基因在灵长类动物中是单拷贝的,并且包含在其他物种中高度不同的区域。XBR在B细胞系中的过表达导致由DPA启动子驱动的报告基因构建体的转录显著减少,但由X2盒突变的类似构建体则没有。同样,XBR的过表达降低了用IFN-γ处理的HeLa细胞中由DPA启动子驱动的报告基因活性的诱导。因此,XBR可能介导转录抑制,从而防止不适当的MHC II类表达。XBR的功能可能部分解释了细胞融合实验中报道的MHC II类表达的显性反式作用抑制。

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