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人类免疫球蛋白重链基因座J区广泛的等位基因序列变异。

Extensive allelic sequence variation in the J region of the human immunoglobulin heavy chain gene locus.

作者信息

Mattila P S, Schugk J, Wu H, Mäkelä O

机构信息

Department of Bacteriology and Immunology, University of Helsinki, Finland.

出版信息

Eur J Immunol. 1995 Sep;25(9):2578-82. doi: 10.1002/eji.1830250926.

Abstract

During the initial stages of B lymphocyte differentiation heavy chain variable (VH), diversity (DH) and joining (JH) gene segments recombine to form a functional heavy chain variable region (VDJ) gene. Evidence for genetic polymorphism of the human JH gene segments has been obtained from mature rearranged VDJ sequences. We conducted an analysis of the published rearranged JH gene sequences and found that the JH alleles present in the two published germ-line JH region sequences were rare (approx. 2%) in the rearranged sequences. As an attempt to explain this discrepancy a 2.5-kb strech of DNA containing all the six heavy chain JH region genes and the most 3' DH gene segment, DHQ52, was amplified by the polymerase chain reaction from 39 individuals and analyzed for restriction fragment length polymorphism. Five new JH region haplotypes were found and sequenced. These new haplotypes contained the coding segment alleles that were frequent in antibody genes. Surprisingly, a high number of interallelic differencies in the non-coding sequence was found between the new and the two previously published haplotypes implying that the haplotypes had been separated early in evolution. In this respect the JH locus resembles HLA loci.

摘要

在B淋巴细胞分化的初始阶段,重链可变区(VH)、多样性区(DH)和连接区(JH)基因片段发生重排,形成功能性重链可变区(VDJ)基因。人类JH基因片段遗传多态性的证据已从成熟的重排VDJ序列中获得。我们对已发表的重排JH基因序列进行了分析,发现两个已发表的种系JH区域序列中存在的JH等位基因在重排序列中很罕见(约2%)。为了解释这种差异,我们通过聚合酶链反应从39名个体中扩增出一段包含所有六个重链JH区域基因和最3'端DH基因片段DHQ52的2.5kb DNA片段,并对其进行限制性片段长度多态性分析。发现了五种新的JH区域单倍型并进行了测序。这些新的单倍型包含在抗体基因中常见的编码区段等位基因。令人惊讶的是,在新的单倍型与之前发表的两种单倍型之间的非编码序列中发现了大量等位基因间差异,这意味着这些单倍型在进化早期就已分离。在这方面,JH基因座类似于HLA基因座。

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