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Journal of Virology, May 2001, p. 4902-4906, Vol. 75, No. 10
Departments of
Microbiology1 and Cell
Biology,2 University of Alabama at
Birmingham, Birmingham, Alabama 35294
Received 14 November 2000/Accepted 19 February 2001
A mutant human immunodeficiency virus type 1 (HIV-1) with a primer
binding site (PBS) complementary to yeast tRNAPhe
(psHIV-Phe), which relies on exogenous yeast tRNAPhe as
reverse transcription primer, was used to investigate elements in the
tRNA acceptor stem and T
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.10.4902-4906.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Identification of Critical Elements in the tRNA
Acceptor Stem and T
C Loop Necessary for Human Immunodeficiency
Virus Type 1 Infectivity
C stem-loop required for the tRNA primer
selection and use in HIV-1 replication. tRNAPhe mutants
with two- or four-nucleotide deletions in the 3' end retained the
capacity to complement replication of psHIV-Phe. tRNAPhe
mutants with an extended 5' end had reduced capacity for
complementation, which could be restored by extension of the 3' end of
these tRNAPhe mutants with sequences complementary to the
HIV-1 U5 region. Further analysis of mutations in the acceptor stem of
tRNAPhe suggested that an intact acceptor stem RNA
structure is important for complementation. Analysis of
single-nucleotide changes in the T
C stem-loop of tRNAPhe
revealed an unexpected, essential role of this region for rescue of
psHIV-Phe.
*
Corresponding author. Mailing address: Departments of
Microbiology and Cell Biology, University of Alabama at Birmingham, Birmingham, AL 35294. Phone: (205) 934-5705. Fax: (205) 934-1580. E-mail: casey_morrow{at}uab.edu.
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