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导致等位基因排斥的免疫球蛋白κ轻链基因座的新型重组。

Novel recombinations of the IG kappa-locus that result in allelic exclusion.

作者信息

Feddersen R M, Martin D J, Van Ness B G

机构信息

Department of Biochemistry, University of Iowa City 52242.

出版信息

J Immunol. 1990 Jul 15;145(2):745-50.

PMID:2114448
Abstract

Allelic exclusion of Ig H and L chain gene loci serves to ensure that a B cell expresses a single specificity antibody. The analysis of Abelson murine leukemia virus transformed cells that rearrange the kappa-locus during growth in cell culture has provided the opportunity to characterize intermediate steps in Ig gene rearrangement. By sequential cloning of an Abelson murine leukemia virus transformed cell line we have observed a novel two-step pathway that results in a rearrangement of a V kappa gene segment into the J-C kappa intron. This type of rearrangement effectively excludes functional kappa expression from that allele. A truncated mRNA product resulting from the V kappa signal exon splicing to the C kappa exon is diagnostic of these unique rearrangements. In addition to demonstrating a novel mechanism for allelic exclusion, the two-step pathway described serves to explain how V-intron recombination products were generated in previously described cell lines.

摘要

免疫球蛋白重链和轻链基因座的等位基因排斥作用有助于确保B细胞表达单一特异性抗体。对在细胞培养生长过程中重排κ基因座的艾贝尔森鼠白血病病毒转化细胞的分析,为表征免疫球蛋白基因重排的中间步骤提供了机会。通过对艾贝尔森鼠白血病病毒转化细胞系进行连续克隆,我们观察到一种新的两步途径,该途径导致Vκ基因片段重排至J-Cκ内含子中。这种重排类型有效地从该等位基因中排除了功能性κ链的表达。由Vκ信号外显子剪接至Cκ外显子产生的截短mRNA产物是这些独特重排的诊断依据。除了证明等位基因排斥的新机制外,所描述的两步途径还用于解释在先前描述的细胞系中是如何产生V-内含子重组产物的。

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