TY - JOUR
T1 - The effect of increased processivity on overall fidelity of human immunodeficiency virus type 1 reverse transcriptase
AU - Rezende, L. F.
AU - Kew, Y.
AU - Prasad, V. R.
N1 - Funding Information:
This work was supported by Public Health Service grant AI40375 (to VRP). The authors wish to thank William Drosopoulos, Tim Fisher, Scott Garforth and William Franklin for reading the manuscript and the Oligonucleotide Synthesis Facility of the Albert Einstein College of Medicine's Cancer Center for DNA oligonucleotides.
PY - 2001
Y1 - 2001
N2 - We previously reported that two insertions of 15 amino acids in the β3-β4 hairpin loop of fingers subdomain of HIV-1NL4-3 RT confer an increased polymerase processivity. The processivity of human immunodeficiency virus (HIV) reverse transcriptase (RT) is thought to influence the fidelity of HIV-1 RT, which tends to create errors at template sites with high termination probability. Employing the two insertion variants of HIV-1 RT (FE20 and FE103), we examined the relationship between processivity, overall fidelity and error specificity. Although the overall mutation rate was unaffected by increased processivity, one of the mutants, FE103, generated significantly fewer frameshift errors. The other mutant, FE20, generated errors at hotspots not previously observed for HIV-1 RT. Our results indicate that an increase in the polymerase processivity of HIV-1 RT does not necessarily result in a decreased mutation rate and confirm that changes in processivity alter the sequence context in which the errors are made. Furthermore, our results also reveal that the mutation frequency obtained via in vitro gap-filling reactions with wild-type HIV-1NL4-3 RT is only 2-fold higher than that obtained via a single cycle infection assay using the same, wild-type HIV-1NL4-3 RT sequence as part of the helper pol function [Mansky and Temin: J Virol 69:5087-5094;1995].
AB - We previously reported that two insertions of 15 amino acids in the β3-β4 hairpin loop of fingers subdomain of HIV-1NL4-3 RT confer an increased polymerase processivity. The processivity of human immunodeficiency virus (HIV) reverse transcriptase (RT) is thought to influence the fidelity of HIV-1 RT, which tends to create errors at template sites with high termination probability. Employing the two insertion variants of HIV-1 RT (FE20 and FE103), we examined the relationship between processivity, overall fidelity and error specificity. Although the overall mutation rate was unaffected by increased processivity, one of the mutants, FE103, generated significantly fewer frameshift errors. The other mutant, FE20, generated errors at hotspots not previously observed for HIV-1 RT. Our results indicate that an increase in the polymerase processivity of HIV-1 RT does not necessarily result in a decreased mutation rate and confirm that changes in processivity alter the sequence context in which the errors are made. Furthermore, our results also reveal that the mutation frequency obtained via in vitro gap-filling reactions with wild-type HIV-1NL4-3 RT is only 2-fold higher than that obtained via a single cycle infection assay using the same, wild-type HIV-1NL4-3 RT sequence as part of the helper pol function [Mansky and Temin: J Virol 69:5087-5094;1995].
KW - Forward mutation rate
KW - HIV-1 reverse transcriptase
KW - Polymerase processivity
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U2 - 10.1159/000054033
DO - 10.1159/000054033
M3 - Article
C2 - 11287751
AN - SCOPUS:0035073263
SN - 1021-7770
VL - 8
SP - 197
EP - 205
JO - Journal of Biomedical Science
JF - Journal of Biomedical Science
IS - 2
ER -