Unselected mutations in the human immunodeficiency virus type 1 genome are mostly nonsynonymous and often deleterious

被引:58
作者
Gao, F
Chen, Y
Levy, DN
Conway, JA
Kepler, TB
Hui, HX
机构
[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Dept Biostat & Bioinformat, Durham, NC 27710 USA
[3] Duke Univ, Ctr Bioinformat & Computat Biol, Inst Genome Sci & Policy, Durham, NC 27710 USA
[4] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
关键词
D O I
10.1128/JVI.78.5.2426-2433.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mutation rates of human immunodeficiency virus type 1 (HIV-1) genomes have been estimated using purified reverse transcriptase or single-round infection system. Since small sequences were used as templates, the overall mutation rates could only be extrapolated and the biological significance of mutations is unknown. For direct estimation of HIV-1 mutation rates and understanding of the potential biological influences of mutations, we obtained 19 complete or nearly full-length proviral genomes from single-round-infected adherent cells of lymphocytes by using a lambda phage library method and a long-range PCR technique. Analysis of 160,000 lip of sequences showed that the overall mutation rate of HIV-1 genomes was 5.4 X 10(-5) per base per replication cycle. On average, 1.1 mutations (range, 0 to 3) were generated in each viral genome during one infection cycle. Inspection of the mutations in the HIV-1 genome revealed that all site mutations within protein-coding regions were nonsynonymous mutations. Among all mutations, half were deleterious (premature stop codon and deletions) and would result in defective genomes. By applying the same system to an HIV-1 genome with a G262A mutation in the thumb region of the reverse transcriptase, a significant increase was observed in deletion and insertion mutation rates but no increase in the overall mutation rate in viral genomes was found.
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页码:2426 / 2433
页数:8
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