Previous Article | Next Article ![]()
Journal of Virology, August 2000, p. 7171-7178, Vol. 74, No. 15
Department of
Biochemistry1 and Department of
Microbiology and Immunology,3 West Virginia
University, Morgantown, West Virginia 26506, and HIV Drug
Resistance Program, National Cancer Institute, Frederick Cancer
Research and Development Center, Frederick, Maryland
217022
Received 24 February 2000/Accepted 8 May 2000
Retroviral reverse transcriptases (RTs) frequently switch templates
within the same RNA or between copackaged viral RNAs to generate
mutations and recombination. To identify structural elements of murine
leukemia virus RT important for template switching, we developed an in
vivo assay in which RT template switching within direct repeats
functionally reconstituted the green fluorescent protein gene. We
quantified the effect of mutations in the YXDD motif, the
deoxynucleoside triphosphate binding site, the thumb domain, and the
RNase H domain of RT and hydroxyurea treatment on the frequencies of
template switching. Hydroxyurea treatment and some mutations in RT
increased the frequency of RT template switching up to fivefold, while
all of the mutations tested in the RNase H domain decreased the
frequency of template switching by twofold. Based on these results, we
propose a dynamic copy choice model in which both the rate of DNA
polymerization and the rate of RNA degradation influence the frequency
of RT template switching.
0022-538X/00/$04.00+0
Structural Determinants of Murine Leukemia Virus
Reverse Transcriptase That Affect the Frequency of Template
Switching
*
Corresponding author. Mailing address: HIV Drug
Resistance Program, National Cancer Institute, FCRDC, Bldg. 535, Rm.
334, Frederick, MD 21702. Phone: (301) 846-1710. Fax: (301) 846-6013. E-mail: VPATHAK{at}mail.ncifcrf.gov.
This article has been cited by other articles:
| J. Bacteriol. | Mol. Cell. Biol. | Microbiol. Mol. Biol. Rev. |
|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|