Document 0163 DOCN M9650163 TI Strand displacement synthesis of the long terminal repeats by HIV reverse transcriptase. DT 9605 AU Fuentes GM; Rodriguez-Rodriguez L; Palaniappan C; Fay PJ; Bambara RA; Department of Microbiology & Immunology, University of Rochester,; School of Medicine and Dentistry, New York 14642, USA. SO J Biol Chem. 1996 Jan 26;271(4):1966-71. Unique Identifier : AIDSLINE MED/96147167 AB According to the current model for retroviral replication, strand displacement of the long terminal repeat (LTR) is a necessary step during plus strand DNA synthesis in vivo. We have investigated the ability of human immunodeficiency virus reverse transcriptase (HIV-RT) to synthesize in vitro over a 634-nucleotide HIV LTR DNA template, having or lacking a single full-length DNA downstream primer. The presence of the downstream primer resulted in an approximately 12-fold reduction in the rate of upstream primer elongation. Addition of Escherichia coli single-stranded binding protein (SSB) or human replication protein A (RP-A) enhanced strand displacement synthesis; however, addition of HIV nucleocapsid protein (NC) did not. The presence of excess single-stranded DNA complementary to the downstream primer did not stimulate displacement synthesis. Interestingly, we observed that the elongating upstream primer could readily transfer to this DNA. This observation suggests that recombination is favored during strand displacement synthesis in vivo. DE Base Sequence DNA Primers/CHEMISTRY DNA-Binding Proteins/METABOLISM DNA, Single-Stranded/METABOLISM DNA, Viral/*BIOSYNTHESIS Human HIV Long Terminal Repeat/*GENETICS HIV-1/*ENZYMOLOGY/GENETICS Molecular Sequence Data RNA-Directed DNA Polymerase/*METABOLISM Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. Templates Virus Replication JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).