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HIV-1 Rev的过表达促进非分裂真核细胞的死亡。

Over-expression of the HIV-1 Rev promotes death of nondividing eukaryotic cells.

作者信息

Levin Aviad, Hayouka Zvi, Friedler Assaf, Loyter Abraham

机构信息

Department of Biological Chemistry, The Alexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel.

出版信息

Virus Genes. 2010 Jun;40(3):341-6. doi: 10.1007/s11262-010-0458-7. Epub 2010 Feb 12.

Abstract

Expression of the human immunodeficiency virus type 1 (HIV-1) Rev protein is essential for completion of the viral life cycle. Rev mediates nuclear export of partially spliced and unspliced viral transcripts and therefore bears a nuclear localization signal (NLS) as well as a nuclear export signal (NES), which allow its nucleocytoplasmic shuttling. Attempts to express the wild-type Rev protein in eukaryotic human cultured cells have encountered difficulties and so far have failed. Here we show that accumulation of Rev, which occurs in nondividing Rev-expressing cells or when such cells reach confluency, results in death of these cells. Cell death was also promoted by addition of a cell permeable peptide bearing the Rev-NES sequence, but not by the Rev-NLS peptide. Our results probably indicate that binding of excess amounts of the Rev protein or the NES peptide to the exportin receptor CRM1 results in cells' death.

摘要

1型人类免疫缺陷病毒(HIV-1)Rev蛋白的表达对于病毒生命周期的完成至关重要。Rev介导部分剪接和未剪接的病毒转录本的核输出,因此带有一个核定位信号(NLS)以及一个核输出信号(NES),这使得它能够在细胞核与细胞质之间穿梭。在真核人类培养细胞中表达野生型Rev蛋白的尝试遇到了困难,迄今为止均告失败。在此我们表明,Rev的积累发生在不分裂的Rev表达细胞中或此类细胞达到汇合状态时,会导致这些细胞死亡。添加带有Rev-NES序列的细胞可渗透肽也会促进细胞死亡,但Rev-NLS肽则不会。我们的结果可能表明,过量的Rev蛋白或NES肽与输出蛋白受体CRM1结合会导致细胞死亡。

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