Posttranscriptional Regulation in Herpes Simplex Virus

Anne Phelan , J.Barklie Clements
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引用次数: 29

Abstract

The essential herpes simplex virus type 1 (HSV-1) immediate-early protein IE63 (ICP27) is an RNA binding protein which, at the posttranscriptional level, interacts with cellular splicing small nuclear ribonucleoprotein particles (snRNPs) and inhibits RNA splicing, promotes RNA 3′ processing, and prevents the nucleocytoplasmic transport of intron-containing mRNAs. IE63 is the only HSV IE protein with homologs not only among other α herpesviruses, but also throughout the herpesviridae family. Recent evidence shows that IE63 is a nucleocytoplasmic shuttle protein able to travel from snRNP- and RNA-rich nuclear foci to the cytoplasm. This property suggests that IE63 may facilitate the nuclear export of virus mRNAs, perhaps selectively, of HSV-1 transcripts, from virus genes which lack introns. Posttranscriptional effects of other HSV-1 functions are discussed.

单纯疱疹病毒的转录后调控
原发性单纯疱疹病毒1型(HSV-1)即时早期蛋白IE63 (ICP27)是一种RNA结合蛋白,在转录后水平上与细胞剪接小核核糖核蛋白颗粒(snRNPs)相互作用,抑制RNA剪接,促进RNA 3 '加工,并阻止内含子mrna的核胞质转运。IE63是唯一的HSV IE蛋白,不仅在其他α疱疹病毒中有同源物,而且在整个疱疹病毒科中都有同源物。最近的证据表明,IE63是一种核细胞质穿梭蛋白,能够从富含snRNP和rna的核灶到细胞质。这一特性表明,IE63可能有助于从缺乏内含子的病毒基因中选择性地输出HSV-1转录本的病毒mrna。讨论了其他HSV-1功能的转录后效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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