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人类免疫球蛋白重链基因簇内的多个基因缺失。

Multiple gene deletions within the human immunoglobulin heavy-chain cluster.

作者信息

Migone N, Oliviero S, de Lange G, Delacroix D L, Boschis D, Altruda F, Silengo L, DeMarchi M, Carbonara A O

出版信息

Proc Natl Acad Sci U S A. 1984 Sep;81(18):5811-5. doi: 10.1073/pnas.81.18.5811.

Abstract

Two subjects, of 11,000 healthy individuals screened, were found to be missing three and four immunoglobulin isotypes, respectively (IgA1, IgG2, and IgG4; IgA1, IgG2, IgG4, and IgE), and have been analyzed at the DNA level by means of Southern blotting and Ig heavy-chain-specific probes. A broad deletion within the heavy-chain constant region (C) gene cluster was found on chromosome 14 of both probands. Two different haplotypes are described: the first has lost the C alpha 1, C psi gamma, C gamma 2, C gamma 4, and C epsilon genes; the second lacks the C psi epsilon, C alpha 1, C psi gamma, C gamma 2, and C gamma 4 genes. These findings confirm the reciprocal order of the Ig heavy-chain genes as derived by molecular cloning. The inclusion of the C psi gamma gene within the deleted regions confirms its location between C alpha 1 and C gamma 2. From the observed frequency of the homozygous genotype, 1%-3% of healthy subjects from our population are expected to be heterozygous for multiple heavy-chain gene deletions. Cross-over between mispaired homologous regions seems to be the favored mechanism of multiple Ig gene deletions and duplications, and, generally, in the evolution of the human Ig heavy-chain gene family.

摘要

在筛查的11000名健康个体中,有两名分别缺失三种和四种免疫球蛋白同种型(分别为IgA1、IgG2和IgG4;IgA1、IgG2、IgG4和IgE),并已通过Southern印迹法和Ig重链特异性探针在DNA水平进行了分析。在两名先证者的14号染色体上均发现了重链恒定区(C)基因簇内的广泛缺失。描述了两种不同的单倍型:第一种缺失了Cα1、Cψγ、Cγ2、Cγ4和Cε基因;第二种缺失了Cψε、Cα1、Cψγ、Cγ2和Cγ4基因。这些发现证实了通过分子克隆得出的Ig重链基因的相互顺序。缺失区域内包含Cψγ基因证实了其位于Cα1和Cγ2之间。根据观察到的纯合基因型频率,预计我们人群中1%-3%的健康受试者为多重重链基因缺失的杂合子。错配同源区域之间的交叉似乎是多重Ig基因缺失和重复以及一般人类Ig重链基因家族进化中最常见的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d580/391801/954c99efa3ad/pnas00619-0196-a.jpg

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