Levin Aviad, Hayouka Zvi, Friedler Assaf, Loyter Abraham
Department of Biological Chemistry, The Alexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel.
Virus Genes. 2010 Jun;40(3):341-6. doi: 10.1007/s11262-010-0458-7. Epub 2010 Feb 12.
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.
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。