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对RFX5编码基因的突变及染色体定位分析,RFX5是一种在主要组织相容性复合体II类缺陷中受影响的新型转录因子。

Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency.

作者信息

Villard J, Reith W, Barras E, Gos A, Morris M A, Antonarakis S E, Van den Elsen P J, Mach B

机构信息

Department of Genetics and Microbiology, University of Geneva Medical School, Switzerland.

出版信息

Hum Mutat. 1997;10(6):430-5. doi: 10.1002/(SICI)1098-1004(1997)10:6<430::AID-HUMU3>3.0.CO;2-H.

Abstract

MHC class II deficiency is a severe primary immunodeficiency characterised by the absence of major histocompatibility complex class II (MHC-II) gene expression. It is genetically heterogeneous and can result from defects in at least four different trans-acting regulatory genes required for transcription of MHC-II genes. One of these genes has recently been shown to encode a novel DNA binding protein called RFX5, which is one subunit of a heteromeric protein complex (RFX) that binds to the promoters of MHC-II genes. We have characterised the mutations in all four patients known to harbour a defect in the RFX5 gene and have mapped this new human disease gene to chromosome 1 band q21, a region frequently exhibiting chromosomal aberrations in a variety of preneoplastic and neoplastic diseases.

摘要

MHC II类缺陷是一种严重的原发性免疫缺陷病,其特征是主要组织相容性复合体II类(MHC-II)基因不表达。它具有遗传异质性,可能由MHC-II基因转录所需的至少四个不同反式作用调节基因的缺陷引起。最近发现其中一个基因编码一种名为RFX5的新型DNA结合蛋白,它是与MHC-II基因启动子结合的异源蛋白复合物(RFX)的一个亚基。我们已对已知携带RFX5基因缺陷的所有四名患者的突变进行了特征分析,并将这个新的人类疾病基因定位到1号染色体q21带,该区域在多种肿瘤前期和肿瘤性疾病中经常出现染色体畸变。

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