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巴西利厄兔缺乏K1b9轻链可能是由于mRNA剪接受体位点的突变。

Lack of K1b9 light chains in Basilea rabbits is probably due to a mutation in an acceptor site for mRNA splicing.

作者信息

Lamoyi E, Mage R G

出版信息

J Exp Med. 1985 Oct 1;162(4):1149-60. doi: 10.1084/jem.162.4.1149.

Abstract

Rabbits of the Basilea strain do not produce normal K1b9 light chains but continue to produce immunoglobulins with light chains of the rare K2 isotype and of lambda type. To understand the molecular basis for this unusual expression of kappa light chains in Basilea rabbits, we undertook an analysis of their kappa genes. We isolated and sequenced the mutant kappa 1b9 gene and found a substitution of A for G in the highly conserved AG dinucleotide of the 3' acceptor splice site. Although we cannot rule out additional alterations of portions of the gene we did not sequence, this spontaneous change of the G found in the normal gene provides a likely molecular explanation for the loss of K1 light chain expression in Basilea rabbits.

摘要

巴西利厄斯品系的兔子不产生正常的K1b9轻链,而是继续产生具有罕见K2同种型轻链和λ型轻链的免疫球蛋白。为了了解巴西利厄斯兔子中κ轻链这种异常表达的分子基础,我们对它们的κ基因进行了分析。我们分离并测序了突变的κ1b9基因,发现在3' 剪接受体位点高度保守的AG二核苷酸中,A取代了G。尽管我们不能排除未测序基因部分的其他改变,但正常基因中发现的G的这种自发变化为巴西利厄斯兔子中K1轻链表达缺失提供了一个可能的分子解释。

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