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HLA 连锁补体基因及 RCA 连锁群的分子定位

Molecular mapping of the HLA-linked complement genes and the RCA linkage group.

作者信息

Campbell R D, Dunham I, Sargent C A

机构信息

MRC Immunochemistry Unit, Department of Biochemistry, University of Oxford, UK.

出版信息

Exp Clin Immunogenet. 1988;5(2-3):81-98.

PMID:3155403
Abstract

Phenotypic genetics have established linkage of the genes encoding proteins involved in the activation of the complement component C3. C2, factor B and C4, three of the structural components of the classical and alternative pathway C3 convertases, are encoded by genes which have been mapped to the class III region of the major histocompatibility complex (MHC) on human chromosome 6. The regulatory proteins factor H, C4BP, CR1, CR2 and DAF, which are involved in the control of C3 convertase activity, are encoded by closely linked genes, termed the regulators of complement activation (RCA) linkage group, that have been mapped to human chromosome 1. cDNA clones for all these proteins have been isolated, and this has made it possible to investigate the organization and structure of the MHC class III genes and the genes in the RCA linkage group. This short review summarizes some of the main features which have emerged from recent cloning work.

摘要

表型遗传学已证实,编码参与补体成分C3激活的蛋白质的基因之间存在连锁关系。C2、B因子和C4是经典途径和替代途径C3转化酶的三个结构成分,它们由已定位到人类6号染色体主要组织相容性复合体(MHC)Ⅲ类区域的基因编码。参与C3转化酶活性控制的调节蛋白H因子、C4结合蛋白(C4BP)、补体受体1(CR1)、补体受体2(CR2)和衰变加速因子(DAF),由紧密连锁的基因编码,这些基因被称为补体激活调节因子(RCA)连锁群,已定位到人类1号染色体。所有这些蛋白质的cDNA克隆均已分离出来,这使得研究MHCⅢ类基因以及RCA连锁群中的基因的组织和结构成为可能。这篇简短的综述总结了近期克隆工作中出现的一些主要特征。

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