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一种替代的15 kDa JC κ蛋白由人类B细胞前体与μ重链结合表达。

A surrogate 15 kDa JC kappa protein is expressed in combination with mu heavy chain by human B cell precursors.

作者信息

Francés V, Pandrau-Garcia D, Guret C, Ho S, Wang Z, Duvert V, Saeland S, Martinez-Valdez H

机构信息

Schering-Plough, Laboratory for Immunology Research, Dardilly, France.

出版信息

EMBO J. 1994 Dec 15;13(24):5937-43. doi: 10.1002/j.1460-2075.1994.tb06939.x.

DOI:10.1002/j.1460-2075.1994.tb06939.x
PMID:7813432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC395569/
Abstract

A novel kappa protein, encoded by a germline JC kappa transcript, is expressed by normal and leukemic human B cell precursors. The transcript displays an open reading frame initiated by a non-AUG codon, and predicts a 15 kDa molecule which could be readily confirmed by in vitro translation. Cellular expression was demonstrated by immunofluorescence, precipitation and Western blotting. Furthermore, 2-D gel electrophoresis revealed that germline JC kappa can covalently associate with mu heavy chain at the surface of pre-B cells. We therefore propose that during B cell lymphopoiesis, two alternative pathways could be operative in which mu heavy chain can either associate with lambda 5 or germ-line JC kappa.

摘要

一种由种系JC κ转录本编码的新型κ蛋白,由正常和白血病人类B细胞前体表达。该转录本显示出由非AUG密码子起始的开放阅读框,并预测出一个15 kDa的分子,这可以通过体外翻译很容易地得到证实。通过免疫荧光、沉淀和蛋白质印迹法证实了细胞表达。此外,二维凝胶电泳显示种系JC κ可以在pre-B细胞表面与μ重链共价结合。因此,我们提出在B细胞淋巴细胞生成过程中,可能存在两种替代途径,其中μ重链可以与λ5或种系JC κ结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/7719dc20f4cc/emboj00072-0157-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/7ca9ac38913c/emboj00072-0153-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/9739a8824a5b/emboj00072-0154-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/3b2d24cc3644/emboj00072-0154-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/f31e2264ed10/emboj00072-0156-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/769e86b08abf/emboj00072-0157-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/7719dc20f4cc/emboj00072-0157-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/7ca9ac38913c/emboj00072-0153-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/9739a8824a5b/emboj00072-0154-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/3b2d24cc3644/emboj00072-0154-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/f31e2264ed10/emboj00072-0156-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/769e86b08abf/emboj00072-0157-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f67/395569/7719dc20f4cc/emboj00072-0157-b.jpg

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本文引用的文献

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近端Jκ种系转录本启动子通过控制有序重组促进受体编辑。
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