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在人类细胞中,两个等位基因上免疫球蛋白κ基因的重排并非免疫球蛋白λ基因表达的必要前提条件。

Re-organization of the immunoglobulin kappa gene on both alleles is not an obligatory prerequisite for Ig lambda gene expression in human cells.

作者信息

Abken H, Bützler C

机构信息

Institut für Genetik, Abt. Molekulargenetik, Universität Bonn, Germany.

出版信息

Immunology. 1991 Dec;74(4):709-13.

Abstract

Re-arrangement and expression of the immunoglobulin (Ig) genes in B cells occurs under an ordered developmental control. The sequential model of Ig light chain exclusion predicts that only after non-productive re-organization or deletion of both Ig kappa alleles would re-arrangement of Ig lambda gene segments occur. To prove this model, we asked whether expression of Ig lambda light chains is always associated with rearrangement and/or deletion of both Ig kappa alleles in human cells. Therefore, we established human diploid B-cell clones in vitro that produce Ig lambda light chains. Southern blot analysis of the Ig kappa alleles revealed that three Ig lambda expressing cell lines (out of six Ig lambda+ cell lines tested) harbour one Ig kappa allele in germline configuration. Furthermore, a 1.5 kb RNA derived from the germline Ig kappa locus was detected by Northern blot hybridizations. The results implicate that the mechanism of Ig light chain exclusion is not precisely sequential and that it does not necessarily need re-arrangement or deletion of both Ig kappa alleles as a prerequisite for Ig lambda light chain expression in human cells.

摘要

B细胞中免疫球蛋白(Ig)基因的重排和表达是在有序的发育控制下发生的。Ig轻链排除的顺序模型预测,只有在两个Igκ等位基因发生非生产性重排或缺失后,Igλ基因片段才会发生重排。为了验证这一模型,我们研究了在人类细胞中,Igλ轻链的表达是否总是与两个Igκ等位基因的重排和/或缺失相关。因此,我们在体外建立了产生Igλ轻链的人类二倍体B细胞克隆。对Igκ等位基因的Southern印迹分析显示,在所检测的6个Igλ+细胞系中有3个表达Igλ的细胞系含有一个处于种系构型的Igκ等位基因。此外,通过Northern印迹杂交检测到了来自种系Igκ基因座的1.5 kb RNA。这些结果表明,Ig轻链排除机制并非精确的顺序性,而且在人类细胞中,Igλ轻链表达并不一定需要两个Igκ等位基因的重排或缺失作为前提条件。

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