Residues within the HFRIGC sequence of HIV-1 Vpr involved in growth arrest activities

被引:16
作者
Berglez, JM [1 ]
Castelli, LA [1 ]
Sankovich, SA [1 ]
Smith, SC [1 ]
Curtain, CC [1 ]
Macreadie, IG [1 ]
机构
[1] Biomol Res Inst, Parkville, Vic 3052, Australia
关键词
D O I
10.1006/bbrc.1999.1511
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
HIV-1 Vpr is a virion-associated protein that can cause growth arrest when produced inside the cell but when added externally it can cause cell death. Employing the yeast model system, the C-terminal domain, in particular the sequence HFRIGCRHSRIG (Vpr(71-82)), is essential for both the growth arrest and cytocidal activities. Conservation of this sequence in HIV-2 and SIV suggests that these residues may be functionally important, Using site-directed mutagenesis we show that the most highly conserved aa residues, His71 and Gly75, were important for the cell cycle inhibitory effects. In contrast, we show that the wild-type Vpr(71-82) peptide and three variants of this peptide with Gly75 changed to Ser, Ala, and ne all exhibited the same cytocidal activity suggesting that the intracellular and extracellular effects are unrelated. (C) 1999 Academic Press.
引用
收藏
页码:287 / 290
页数:4
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