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人类B细胞个体发育过程中假轻链基因的组织与表达

Organization and expression of the pseudo-light chain genes in human B-cell ontogeny.

作者信息

Schiff C, Milili M, Bossy D, Fougereau M

机构信息

Centre d'immunologie INSERM-CNRS de Marseille-Luminy, Marseille, France.

出版信息

Int Rev Immunol. 1992;8(2-3):135-45. doi: 10.3109/08830189209055569.

Abstract

In pre-B cells, the mu chain is expressed at the cell surface in association with a "light chain surrogate" encoded by the V pre-B and the lambda-like genes. This mu-psi-L complex presumably triggers early steps of the B cell differentiation, possibly by controlling the Ig gene rearrangements. In the humans, the lambda-like complex contains 3 genes, located in the 22q11.2-q12.3 band, telomeric to the IGCL locus, with which they share a similar organization, pointing to a common genetic origin. Only one lambda-like gene, 14.1, is functional and specifically expressed with V pre-B in pre-B cells. This expression starts in cells which still have the IGH locus in germline configuration (pro-B stage) and ceases as soon as the IGL loci rearrange. These pre-B specific transcripts provide useful markers of cells of the B lineage in both physiological and pathological situations.

摘要

在前B细胞中,μ链与由V前B基因和类λ基因编码的“替代轻链”一起表达于细胞表面。这种μ-ψ-L复合物可能通过控制Ig基因重排来触发B细胞分化的早期步骤。在人类中,类λ复合物包含3个基因,位于22q11.2-q12.3带,在IGCL基因座的端粒位置,它们与IGCL基因座具有相似的组织结构,表明有共同的遗传起源。只有一个类λ基因,即14.1基因,具有功能并在前B细胞中与V前B基因特异性共表达。这种表达在仍具有种系构型的IGH基因座的细胞(前B细胞阶段)中开始,并在IGL基因座重排后立即停止。这些前B细胞特异性转录本在生理和病理情况下都是B系细胞的有用标志物。

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