Suppr超能文献

一种新型调节性肌球蛋白轻链基因可区分前B细胞亚群,且受白细胞介素-7诱导。

A novel regulatory myosin light chain gene distinguishes pre-B cell subsets and is IL-7 inducible.

作者信息

Oltz E M, Yancopoulos G D, Morrow M A, Rolink A, Lee G, Wong F, Kaplan K, Gillis S, Melchers F, Alt F W

机构信息

Howard Hughes Medical Institute, Boston, MA.

出版信息

EMBO J. 1992 Jul;11(7):2759-67. doi: 10.1002/j.1460-2075.1992.tb05341.x.

Abstract

We describe a novel regulatory myosin light chain gene (termed precursor lymphocyte-specific regulatory light chain or PLRLC) that is expressed specifically in precursor B and T lymphocytes. PLRLC is the first example of a regulatory myosin light chain gene which displays specific expression in non-muscle cells. PLRLC is expressed in adult bone marrow derived normal and transformed pre-B cells; in the former, PLRLC expression levels are induced by the pre-B cell specific growth factor interleukin-7 (IL-7). PLRLC is not expressed in either transformed pre-B cells derived from fetal liver or in normal fetal liver pre-B clones grown in the presence of IL-7. Therefore this gene provides the first marker that clearly distinguishes these two pre-B subsets. Finally, several of the different PLRLC transcripts potentially encode regulatory myosin light chains with unique structural features. The unique distribution, regulation and structural features of the PLRLC gene products suggest an important role for PLRLC during lymphocyte development.

摘要

我们描述了一种新的调节性肌球蛋白轻链基因(称为前体淋巴细胞特异性调节轻链或PLRLC),它在前体B淋巴细胞和T淋巴细胞中特异性表达。PLRLC是调节性肌球蛋白轻链基因中首个在非肌肉细胞中呈现特异性表达的例子。PLRLC在成年骨髓来源的正常和转化前B细胞中表达;在前者中,PLRLC的表达水平由前B细胞特异性生长因子白细胞介素-7(IL-7)诱导。PLRLC在源自胎儿肝脏的转化前B细胞中均不表达,在存在IL-7的情况下生长的正常胎儿肝脏前B克隆中也不表达。因此,该基因提供了第一个能明确区分这两个前B细胞亚群的标志物。最后,几种不同的PLRLC转录本可能编码具有独特结构特征的调节性肌球蛋白轻链。PLRLC基因产物独特的分布、调控和结构特征表明PLRLC在淋巴细胞发育过程中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4021/556751/86364d330e62/emboj00092-0383-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验