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前B淋巴细胞克隆后代中的κ基因多样性。

kappa gene diversity among the clonal progeny of pre-B lymphocytes.

作者信息

Ziegler S F, Treiman L J, Witte O N

出版信息

Proc Natl Acad Sci U S A. 1984 Mar;81(5):1529-33. doi: 10.1073/pnas.81.5.1529.

Abstract

Some clonal pre-B cell lines, when transformed by Abelson murine leukemia virus, are able to rearrange and express kappa light chain genes. We have analyzed the light chains expressed in sets of early B-cell subclones derived from two pre-B cell clones. Each subclone makes an indistinguishable mu heavy chain, while the kappa gene rearrangements and proteins synthesized were distinct. All members of one set of subclones expressed a V kappa 21 kappa light chain. Only one of the members of the other two sets of subclones expressed V kappa 21. Thus, a single pre-B-cell clone can select a kappa variable region from more than one family. In each subclone of the set that expressed V kappa 21 light chain the same member appears to be used. The differences detected in the expressed proteins can best be explained by primary sequence alterations in the rearranged V kappa 21 segment. These sequence alterations have resulted in a restriction site polymorphism in the expressed V kappa 21 gene and charge and size differences in the expressed proteins. These data suggest that diversification of kappa light chains can occur at the pre-B- to early B-cell stage of development.

摘要

一些克隆性前B细胞系在被阿贝尔森鼠白血病病毒转化后,能够重排并表达κ轻链基因。我们分析了源自两个前B细胞克隆的早期B细胞亚克隆组中所表达的轻链。每个亚克隆产生的μ重链无法区分,而κ基因重排和合成的蛋白质却各不相同。一组亚克隆的所有成员都表达Vκ21κ轻链。另外两组亚克隆中只有一个成员表达Vκ21。因此,单个前B细胞克隆可以从多个家族中选择一个κ可变区。在表达Vκ21轻链的亚克隆组中,似乎使用的是同一个成员。所检测到的表达蛋白的差异最好用重排的Vκ21片段中的一级序列改变来解释。这些序列改变导致了表达的Vκ21基因中的限制性位点多态性以及表达蛋白的电荷和大小差异。这些数据表明,κ轻链的多样化可能发生在前B细胞到早期B细胞的发育阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67e9/344870/aeea0a7a81ce/pnas00606-0250-a.jpg

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