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[核糖核酸酶L,先天性免疫及其他细胞功能的关键介质]

[RNase L, a crucial mediator of innate immunity and other cell functions].

作者信息

Bisbal Catherine, Salehzada Tamim

机构信息

Inserm ERI25-EA 4202, Muscle et Pathologies, Bâtiment Crastes de Paulet, CHU Arnaud de Villeneuve, 371, avenue du Doyen Gaston Giraud, 34295 Montpellier Cedex 5, France.

出版信息

Med Sci (Paris). 2008 Oct;24(10):859-64. doi: 10.1051/medsci/20082410859.

Abstract

The 2-5A/RNase L pathway is one of the first cellular defences against viruses. RNase L is an unusual endoribonuclease which activity is strictly regulated by its binding to a small oligonucleotide, 2-5A. 2-5A itself is very unusual, consisting of a series of 5'- triphosphorylated oligoadenylates with 2'-5' bonds. But RNase L activity is not limited to viral RNA cleavage. RNase L plays a central role in innate immunity, apoptosis, cell growth and differentiation by regulating cellular RNA stability and expression. Default in its activity leads to increased susceptibility to virus infections and to tumor development. RNase L gene has been identified as HPC1 (Hereditary Prostate Cancer 1) gene. Study of RNase L variant R462Q in etiology of prostate cancer has led to the identification of the novel human retrovirus closely related to xenotropic murine leukemia viruses (MuLVs) and named XMRV.

摘要

2-5A/RNase L途径是细胞对病毒的首批防御机制之一。RNase L是一种特殊的内切核糖核酸酶,其活性通过与小寡核苷酸2-5A结合而受到严格调控。2-5A本身也非常特殊,由一系列具有2'-5'键的5'-三磷酸化寡腺苷酸组成。但RNase L的活性并不局限于切割病毒RNA。RNase L通过调节细胞RNA的稳定性和表达,在先天免疫、细胞凋亡、细胞生长和分化中发挥核心作用。其活性缺陷会导致对病毒感染的易感性增加以及肿瘤发展。RNase L基因已被鉴定为HPC1(遗传性前列腺癌1)基因。对前列腺癌病因中RNase L变体R462Q的研究,导致了与嗜异性鼠白血病病毒(MuLVs)密切相关的新型人类逆转录病毒的鉴定,并将其命名为XMRV。

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