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Initiation of in vitro reverse transcription from tRNALys3 on HIV-1 HIV-2 RNAs by both type 1 and 2 reverse transcriptases
被引:9
作者:
Boulmé, F
[1
]
Freund, F
[1
]
Litvak, S
[1
]
机构:
[1] Univ Bordeaux 2, CNRS, EP 630, IFR Pathol Infect 66, F-33077 Bordeaux, France
关键词:
human immunodeficiency virus type 1;
human immunodeficiency virus type 2;
tRNA(Lys3);
reverse transcription;
initiation;
D O I:
10.1016/S0014-5793(98)00649-8
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 reverse transcription is initiated from a cellular tRNA partially associated,vith the retroviral genome. Here we studied homologous HIV-2 cDNa synthesis using natural or synthetic primers, With natural tRNA(Lys3), synthesis of early products comprising nucleotides +5 to +7 preceded the elongation step leading to synthesis of (-) strong-stop cDNA, In the presence of a poly(A)-oligo(dT) trap, no full-length product was observed while early products were still present, showing a transition between initiation and elongation. With DNA primers only an unspecific elongation was found. Our data show a similar mechanism of reverse transcription initiation by HIV-1 and HIV-2 reverse transcriptases. Furthermore, using a heterologous system we found that HIV-I RNA, in contrast to data reported in the literature, was an excellent template for HIV-2 reverse transcriptase. (C) 1998 Federation of European Biochemical Societies.
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页码:165 / 170
页数:6
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