TRANSACTIVATION OF THE MINUS-STRAND DNA TRANSFER BY NUCLEOCAPSID PROTEIN DURING REVERSE TRANSCRIPTION OF THE RETROVIRAL GENOME

被引:159
作者
ALLAIN, B [1 ]
LAPADATTAPOLSKY, M [1 ]
BERLIOZ, C [1 ]
DARLIX, JL [1 ]
机构
[1] ECOLE NORMALE SUPER LYON,INSERM,LABORETRO,F-69364 LYON,FRANCE
关键词
DNA STRAND TRANSFER; NUCLEOCAPSID PROTEIN; RETROVIRUS; REVERSE TRANSCRIPTION;
D O I
10.1002/j.1460-2075.1994.tb06342.x
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
Two DNA strand transfers are required during reverse transcription of the RNA genome of retroviruses to complete provirus synthesis. To understand more about the first strand transfer reaction, that of the minus-strand DNA from the 5' to the 3' end of the retroviral genome, we devised an in vitro system mimicking the Moloney murine leukemia virus reverse transcription process. Two RNAs corresponding to the 5' and 3' regions of the genome were used to perform reverse transcription assays. The role of the nucleocapsid protein NCp10, which is tightly bound to the genome in the virus, was investigated in this system as well as the requirement of the 5' and 3' terminal repeats (R sequences) and the poly(A) tail. The results show that NCp10 drastically enhances the strand transfer reaction and that interactions between reverse transcriptase, nucleocapsid protein and viral RNA may be important. Both R sequences are required for an efficient and accurate DNA strand transfer and the poly(A) tail facilitates this reaction. Furthermore, it is probable that both intra- and intermolecular DNA strand transfers occur when the 5' and 3' ends of the genome are present on the same molecule.
引用
收藏
页码:973 / 981
页数:9
相关论文
共 30 条
[1]   ANALYSIS OF THE INTERACTIONS OF HIV-1 REPLICATION PRIMER TRANSFER RNA(LYS,3) WITH NUCLEOCAPSID PROTEIN AND REVERSE-TRANSCRIPTASE [J].
BARAT, C ;
SCHATZ, O ;
LEGRICE, S ;
DARLIX, JL .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 231 (02) :185-190
[2]   HIV-1 REVERSE-TRANSCRIPTASE SPECIFICALLY INTERACTS WITH THE ANTICODON DOMAIN OF ITS COGNATE PRIMER TRANSFER-RNA [J].
BARAT, C ;
LULLIEN, V ;
SCHATZ, O ;
KEITH, G ;
NUGEYRE, MT ;
GRUNINGERLEITCH, F ;
BARRESINOUSSI, F ;
LEGRICE, SFJ ;
DARLIX, JL .
EMBO JOURNAL, 1989, 8 (11) :3279-3285
[3]   VIRAL-DNA SYNTHESIZED INVITRO BY AVIAN RETROVIRUS PARTICLES PERMEABILIZED WITH MELITTIN .1. KINETICS OF SYNTHESIS AND SIZE OF MINUS-STRAND AND PLUS-STRAND TRANSCRIPTS [J].
BOONE, LR ;
SKALKA, AM .
JOURNAL OF VIROLOGY, 1981, 37 (01) :109-116
[4]  
CORNILLE F, 1990, INT J PEPT PROT RES, V36, P551
[5]   NEW PROCEDURE FOR DIRECT ANALYSIS OF INVITRO REVERSE TRANSCRIPTION OF ROUS-SARCOMA VIRUS-RNA [J].
DARLIX, JL ;
BROMLEY, PA ;
SPAHR, PF .
JOURNAL OF VIROLOGY, 1977, 22 (01) :118-129
[6]  
DARLIX JL, 1993, CR ACAD SCI III-VIE, V316, P763
[7]   CIS ELEMENTS AND TRANS-ACTING FACTORS INVOLVED IN THE RNA DIMERIZATION OF THE HUMAN-IMMUNODEFICIENCY-VIRUS HIV-1 [J].
DARLIX, JL ;
GABUS, C ;
NUGEYRE, MT ;
CLAVEL, F ;
BARRESINOUSSI, F .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 216 (03) :689-699
[8]   ANALYTICAL STUDY OF AVIAN RETICULOENDOTHELIOSIS VIRUS DIMERIC RNA GENERATED INVIVO AND INVITRO [J].
DARLIX, JL ;
GABUS, C ;
ALLAIN, B .
JOURNAL OF VIROLOGY, 1992, 66 (12) :7245-7252
[9]   BINDING-SITES OF VIRAL PROTEIN-P19 ONTO ROUS-SARCOMA VIRUS-RNA AND POSSIBLE CONTROLS OF VIRAL FUNCTIONS [J].
DARLIX, JL ;
SPAHR, PF .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 160 (02) :147-161
[10]  
DEROCQUIGNY H, 1993, NUCLEIC ACIDS RES, V21, P823