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在小鼠正常B细胞发育过程中,免疫球蛋白轻链基因的重排和表达可先于重链表达。

Rearrangement and expression of immunoglobulin light chain genes can precede heavy chain expression during normal B cell development in mice.

作者信息

Novobrantseva T I, Martin V M, Pelanda R, Müller W, Rajewsky K, Ehlich A

机构信息

Institute for Genetics, University of Cologne,Weyertal 121, 50931 Cologne, Germany.

出版信息

J Exp Med. 1999 Jan 4;189(1):75-88. doi: 10.1084/jem.189.1.75.

Abstract

In mouse mutants incapable of expressing mu chains, VkappaJkappa joints are detected in the CD43(+) B cell progenitors. In agreement with these earlier results, we show by a molecular single cell analysis that 4-7% of CD43(+) B cell progenitors in wild-type mice rearrange immunoglobulin (Ig)kappa genes before the assembly of a productive VHDHJH joint. Thus, mu chain expression is not a prerequisite to Igkappa light chain gene rearrangements in normal development. Overall, approximately 15% of the total CD43(+) B cell progenitor population carry Igkappa gene rearrangements in wild-type mice. Together with the results obtained in the mouse mutants, these data fit a model in which CD43(+) progenitors rearrange IgH and Igkappa loci independently, with a seven times higher frequency in the former. In addition, we show that in B cell progenitors VkappaJkappa joining rapidly initiates kappa chain expression, irrespective of the presence of a mu chain.

摘要

在无法表达μ链的小鼠突变体中,在CD43(+) B细胞祖细胞中检测到VκJκ连接。与这些早期结果一致,我们通过分子单细胞分析表明,野生型小鼠中4-7%的CD43(+) B细胞祖细胞在产生有功能的VHDHJH连接之前重排免疫球蛋白(Ig)κ基因。因此,在正常发育过程中,μ链表达不是Igκ轻链基因重排的先决条件。总体而言,野生型小鼠中约15%的总CD43(+) B细胞祖细胞群体携带Igκ基因重排。结合在小鼠突变体中获得的结果,这些数据符合一个模型,即CD43(+)祖细胞独立重排IgH和Igκ基因座,前者的频率高七倍。此外,我们表明,在B细胞祖细胞中,无论μ链是否存在,VκJκ连接都会迅速启动κ链表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5128/1887695/16ebee6b7b92/JEM981510.f1.jpg

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