The frequencies of three mutations conferring resistance to HIV/AIDS were determined in a population sample of native Kuwaitis. The CCR2-64I, SDF1-3ЈA, and CCR5-m303 mutations were detected by polymerase chain reactionrestriction fragment length polymorphism (PCR-RFLP) tests using restriction endonu
A survey for 32 nucleotide deletion in the CCR-5 chemokine receptor gene (Δccr-5) conferring resistance to human immunodeficiency virus type 1 in different ethnic groups and in chimpanzees
✍ Scribed by Voevodin, Alexander; Samilchuk, Elena; Dashti, Suhaila
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 162 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
The 32 nucleotide deletion in the CCR-5 chemokine receptor gene referred to as ⌬ccr-5 has been shown to confer resistance to HIV-1. Using PCR, 1,105 human subjects and 33 common chimpanzees were genotyped attributing them to one of the three possible genotypes: wild-type homozygote (w/w); ⌬ccr-5 homozygote (⌬ccr-5/⌬ccr-5) and ⌬ccr-5/wild-type heterozygotes (⌬ccr-5/w). The ethnic groups investigated included different Middle Eastern nationalities (mainly Arab) and Russians. Carriers of the ⌬ccr-5 mutation were found among Arabs, Iranians and Russians. The highest frequency of the mutation was seen in Russians (24.4% of the ⌬ccr-5 heterozygotes, allele frequency-0.1221). Surprisingly, the only ⌬ccr-5 homozygote identified in our study was an Egyptian. The origin of the ⌬ccr-5 mutation in the Middle Eastern populations, both Arab and non-Arab, is most probably due to a gene flow from the Europeans. The frequency of the ⌬ccr-5 mutation in Russians is one of the highest known. It might be one of the factors contributing to a relatively slow pace of increase in the incidence of sexually acquired HIV infection in Russia. None of the chimpanzees tested was positive for ⌬ccr-5. Interestingly, the DNA sequence of the chimpanzee CCR-5 gene in the region including the site of the ⌬ccr-5 mutation, and flanking areas, was virtually identical to the homologous human sequence, only two mismatches (silent substitutions) were found.
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