Laboratory of Medical Genetics, Harbin Medical University, Baojian Road 157, Nangang District, Harbin, 150081, China.
Mol Biol Rep. 2011 Jan;38(1):327-32. doi: 10.1007/s11033-010-0111-5. Epub 2010 Apr 4.
It has been reported that single nucleotide polymorphisms (SNPs) in the promoter of the CCR5 gene are associated with the risk for HIV-1 infection and AIDS progression. Using resequencing, we performed a systematic survey of 78 HIV-1 seropositive individuals and 70 population-matched healthy control individuals from northern China to investigate SNPs of the CCR5 gene promoter and evaluated their effects on HIV-1 infection and the progression of AIDS. Linkage disequilibrium (LD) plots and haplotypes were generated using Haploview software. The association analyses were statistically compared using the Chi-square test with SPSS13.0 software for Windows. Seven SNPs (58755A>G, 58791C>T, 58934G>T, 59029A>G, 59353C>T, 59402A>G and 59653C>T) in the region of the CCR5 gene promoter were evaluated in this study. Among the seven SNPs, the minor allele frequencies of 58755G and 58791T were less than 2%. The differences in frequencies of the other five SNPs were not significant between case and control cohorts (P>0.05). In the case cohort, the association between these SNPs and clinical features (CD4+ T-lymphocyte counts and clinical categories) was not significant (P>0.05); however, there was a significant association between the haplotype GGTAC and susceptibility to HIV-1 infection (P<0.05), which is not consistent with other reports studied in different populations. The results suggest that the haplotype GGTAC may have a role in the process of HIV-1 infection in the northern Chinese population.
据报道,CCR5 基因启动子中的单核苷酸多态性(SNPs)与 HIV-1 感染和 AIDS 进展的风险相关。我们使用重测序,对来自中国北方的 78 名 HIV-1 血清阳性个体和 70 名人群匹配的健康对照个体进行了系统调查,以研究 CCR5 基因启动子的 SNPs,并评估它们对 HIV-1 感染和 AIDS 进展的影响。使用 Haploview 软件生成连锁不平衡(LD)图谱和单倍型。关联分析使用 Windows 版 SPSS13.0 软件的卡方检验进行统计学比较。本研究评估了 CCR5 基因启动子区域的 7 个 SNPs(58755A>G、58791C>T、58934G>T、59029A>G、59353C>T、59402A>G 和 59653C>T)。在这 7 个 SNP 中,58755G 和 58791T 的次要等位基因频率均小于 2%。病例组和对照组之间其他 5 个 SNP 的频率差异无统计学意义(P>0.05)。在病例组中,这些 SNP 与临床特征(CD4+T 淋巴细胞计数和临床分类)之间没有关联(P>0.05);然而,GGTAC 单倍型与 HIV-1 感染易感性之间存在显著关联(P<0.05),这与在不同人群中研究的其他报告不一致。结果表明,GGTAC 单倍型可能在中国北方人群的 HIV-1 感染过程中起作用。