PARAMETERS THAT INFLUENCE PROCESSIVE SYNTHESIS AND SITE-SPECIFIC TERMINATION BY HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE ON RNA AND DNA TEMPLATES

被引:56
作者
DESTEFANO, JJ
BUISER, RG
MALLABER, LM
FAY, PJ
BAMBARA, RA
机构
[1] UNIV ROCHESTER, MED CTR, DEPT BIOCHEM, POB 607, 601 ELMWOOD AVE, ROCHESTER, NY 14642 USA
[2] UNIV ROCHESTER, DEPT MED, ROCHESTER, NY 14627 USA
[3] UNIV ROCHESTER, CTR CANC, ROCHESTER, NY 14627 USA
关键词
HIV; PROCESSIVE SYNTHESIS; REVERSE TRANSCRIPTASE; VIRAL REPLICATION; RETROVIRUS; AIDS;
D O I
10.1016/0167-4781(92)90025-U
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
We have examined the parameters that determine the length and distribution of products synthesized processively by the human immunodeficiency virus reverse transcriptase (HIV-RT). On native or homopolymer templates, the overall length distribution of processively synthesized products is increased by increased temperature or deoxynucleoside triphosphate concentration, or decreased ionic strength. Specific terminations of processive synthesis on either native DNA or RNA templates occur most frequently at positions where the reverse transcriptase (RT) pauses during synthesis. These sites correlate with the template sequence 3'-(A/U)(A/U)(G/C)-5', particularly when this sequence is predicted to be base paired with another region of the template in a secondary structure. Many positions of termination are in similar positions on DNA or RNA templates. Notable exceptions are runs of A residues, which promote termination on DNA but not RNA templates. Termination intensities vary when different RTs are used demonstrating an influence of RT structure.
引用
收藏
页码:270 / 280
页数:11
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