Differential distribution of compound microsatellites in various Human Immunodeficiency Virus Type 1 complete genomes

► We have surveyed HIV-1 genomes and identified an appreciable number of compound microsatellites. ► The compound microsatellite distribution appears unrelated to geographical locations and subtypes of HIV-1. ► Most compound microsatellites in each HIV-1 genome were found in genic regions. Compound...

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Veröffentlicht in:Infection, genetics and evolution genetics and evolution, 2012-10, Vol.12 (7), p.1452-1457
Hauptverfasser: Chen, Ming, Tan, Zhongyang, Zeng, Guangming, Zeng, Zhuotong
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Sprache:eng
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Zusammenfassung:► We have surveyed HIV-1 genomes and identified an appreciable number of compound microsatellites. ► The compound microsatellite distribution appears unrelated to geographical locations and subtypes of HIV-1. ► Most compound microsatellites in each HIV-1 genome were found in genic regions. Compound microsatellites consist of two or more individual microsatellites, and may originate from dynamic mutations or imperfection of microsatellites. Previous studies have found microsatellites were present in 81 completed Human Immunodeficiency Virus Type 1 (HIV-1) genomes, suggesting compound microsatellites may exist in viral genomes. However, up to now, compound microsatellites have not been analyzed in any viral genomes. We identified and characterized 238 compound microsatellites in 81 completed HIV-1 genomes. About 0–24.24% of all microsatellites could be categorized as compound microsatellites. Compound microsatellite distribution is very different in two aspects between diverse HIV-1 genomes. First, the number and motifs of compound microsatellites are variable between surveyed genomes. Second, the relative abundance and relative density of compound microsatellites exhibit very significant differences between these surveyed genomes, respectively. The relative abundance and relative density of compound microsatellites were weakly correlated with genome size and microsatellite density. We observed a more dynamic picture of compound microsatellites than previously reported in eukaryotes. This might be attributed to the lack of proofreading in HIV-1 genomes, as it has been demonstrated that the loss of polymerase proofreading activity can greatly enhance the mutation rate of microsatellites.
ISSN:1567-1348
1567-7257
DOI:10.1016/j.meegid.2012.05.006