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Genotype and allele frequency of a 32-base pair deletion mutation in the CCR5 gene in various ethnic groups: Absence of mutation among asians and pacific islanders

机译:不同种族的CCR5基因中32个碱基对的缺失突变的基因型和等位基因频率:亚洲人和太平洋岛民中没有突变

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Background: A 32-base pair (bp) deletion mutation in the betachemokine receptor CCR5 gene has been associated with resistance against human immunodeficiency virus type 1 (HIV-1) infection and disease. Large-scale studies conducted among Caucasians indicate that individuals who are homozygous for this deletion mutation (Δ32/Δ32) are protected against HIV-1 infection despite multiple high-risk exposures, whereas CCR5/Δ32 heterozygotes have a slower progression to acquired immunodeficiency syndrome (AIDS).Objective: To determine the genotype and allele frequencies of the CCR5 gene 32-bp deletion mutation among ethnically diverse non-Caucasian populations.Methods: DNA, extracted from blood collected between 1980 and 1997 from 1912 individuals belonging to various ethnic groups, including 363 Caucasians, 303 Puerto Rican Hispanics, 150 Africans, 606 Asians, and 490 Pacific Islanders, were analyzed for the CCR5 gene 32-bp deletion mutation by a polymerase chain reaction (PCR)-based assay, using an oligonucleotide primer pair designed to discriminate CCR5 alleles without restriction endonuclease analysis.Results: The comparative frequency of CCR5/Δ32 heterozygosity was 61 of 363 (16.8%) in Caucasians, 17 of 303 (5.6%) in Puerto Rican Hispanics, 9 of 490 (1.8%) in Pacific Islanders, 0 of 606 (0%) in Asians, and 0 of 150 (0%) in Africans.Conclusions: The data confirm the high frequency of CCR5/Δ32 heterozygosity among Caucasians. Intermediate and low-level Δ32 allele frequencies among Puerto Rican Hispanics and Hawaiians could be attributed to recent European Caucasian gene flow. By contrast, the inability to detect the Δ32 allele among Asians and other Pacific Islander groups suggests that other mechanisms are responsible for resistance to HIV-1 infection in these populations.
机译:背景:β趋化因子受体CCR5基因中的32个碱基对(bp)缺失突变与对人类1型免疫缺陷病毒(HIV-1)感染和疾病的抵抗力有关。在高加索人中进行的大规模研究表明,尽管有多个高风险暴露,但具有这种缺失突变纯合子(Δ32/Δ32)的个体仍可抵御HIV-1感染,而CCR5 /Δ32杂合子进展为获得性免疫缺陷综合征的速度较慢(目的:确定CCR5基因32 bp缺失突变在不同种族的非高加索人群中的基因型和等位基因频率。方法:1980年至1997年从1912个不同种族的人群中采集的血液中提取的DNA,包括363名白种人,303名波多黎各西班牙裔,150名非洲人,606名亚洲人和490名太平洋岛民,通过使用基于设计的寡核苷酸引物对,通过基于聚合酶链反应(PCR)的分析方法分析了CCR5基因32bp缺失突变结果:CCR5 /Δ32杂合子的比较频率为363个中的61个(16.8%),无限制性核酸内切酶分析。高加索人,波多黎各拉美裔裔中的303名中的17名(5.6%),太平洋岛民中490名中的9名(1.8%),亚洲人中606名中的0名(0%),非洲人中150名中的0名(0%)。证实了高加索人中CCR5 /Δ32杂合子的高频率。波多黎各西班牙裔人和夏威夷人之间的中等和低水平Δ32等位基因频率可能归因于最近的欧洲白种人基因流动。相比之下,在亚洲人和其他太平洋岛民群体中无法检测到Δ32等位基因表明,其他机制对这些人群的HIV-1感染具有抵抗力。

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