Venkatesh L K, Chinnadurai G
Institute for Molecular Virology, St. Louis University School of Medicine, Missouri 63110.
Virology. 1990 Sep;178(1):327-30. doi: 10.1016/0042-6822(90)90414-m.
The rev protein (Rev) of human immunodeficiency virus increases the cytoplasmic expression of viral structural gene mRNAs. We had previously reported the existence of a region (residues 73-98) near the carboxy-terminus in HIV-1 Rev essential for its function. To further define the structural elements in this region, we examined the effects of substitution mutations in highly conserved residues in this region, between amino acids 75-81, on Rev function. Mutations in Pro76-77 and Arg80 retained Rev function, whereas those in Leu75 and Leu81 abolished Rev activity and exhibited trans-dominant suppression of wt Rev function. The Leu81 mutation, in particular, exhibited an efficient dominant negative phenotype. Leu75 and Leu81 thus appear to define residues essential to the Rev "effector" function.
人类免疫缺陷病毒的Rev蛋白可增加病毒结构基因mRNA的细胞质表达。我们之前曾报道,HIV-1 Rev蛋白羧基末端附近存在一个对其功能至关重要的区域(第73 - 98位氨基酸)。为进一步明确该区域的结构元件,我们研究了此区域(第75 - 81位氨基酸)高度保守残基的替代突变对Rev功能的影响。Pro76 - 77和Arg80的突变保留了Rev功能,而Leu75和Leu81的突变则消除了Rev活性,并对野生型Rev功能表现出反式显性抑制。特别是Leu81突变表现出高效的显性负性表型。因此,Leu75和Leu81似乎确定了对Rev“效应子”功能至关重要的残基。