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1型人类免疫缺陷病毒Rev蛋白通过核仁功能障碍产生的细胞毒性活性。

Cytotoxic activity of rev protein of human immunodeficiency virus type 1 by nucleolar dysfunction.

作者信息

Nosaka T, Takamatsu T, Miyazaki Y, Sano K, Sato A, Kubota S, Sakurai M, Ariumi Y, Nakai M, Fujita S

机构信息

Institute for Virus Research, Kyoto University, Japan.

出版信息

Exp Cell Res. 1993 Nov;209(1):89-102. doi: 10.1006/excr.1993.1289.

Abstract

The rev protein (Rev) of the human immunodeficiency virus type 1 (HIV-1) is known as a post-transcriptional regulator of viral gene expression. It is located in the cell nucleolus. Transiently expressed Rev caused nucleolar ballooning and deformity with aberrant accumulation of rRNAs, and de novo synthesis of rRNAs decreased dramatically in these cells. However, similarly expressed rex protein (Rex) of the human T-cell leukemia virus type I, which is a functional homologue to Rev, did not affect nucleolar structure and function. Rev expression resulted in cell death with nucleolar destruction in an inducible cell line. Analysis of Rev mutants revealed that both the nucleolar targeting signal of Rev and the multimerization domain are prerequisites to the nucleolar disintegration by Rev. Human T-cells acutely infected with HIV-1 contained nucleoli which were deformed and filled with Rev, but chronically infected cells had intact nucleoli. Involvement of Rev in cytopathic effects in HIV-1 infection is discussed.

摘要

人类免疫缺陷病毒1型(HIV-1)的调控蛋白(Rev)是一种病毒基因表达的转录后调节因子。它位于细胞核仁中。瞬时表达的Rev会导致核仁肿胀和畸形,伴有核糖体RNA(rRNA)的异常积累,并且这些细胞中rRNA的从头合成显著减少。然而,与Rev功能同源的人类T细胞白血病病毒I型的雷克斯蛋白(Rex)经类似表达后,并不会影响核仁的结构和功能。在一个可诱导的细胞系中,Rev表达会导致核仁破坏从而引起细胞死亡。对Rev突变体的分析表明,Rev的核仁靶向信号和多聚化结构域都是Rev导致核仁解体的先决条件。急性感染HIV-1的人类T细胞含有变形且充满Rev的核仁,但慢性感染的细胞具有完整的核仁。本文讨论了Rev在HIV-1感染的细胞病变效应中的作用。

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