Ma Li-ying, Hong Kun-xue, Lu Xiao-zhi, Qin Guang-ming, Chen Jian-ping, Chen Kang-lin, Ruan Yu-hua, Xing Hui, Zhu Jia-hong, Shao Yi-ming
National Center for AIDS/STD Control and Prevention, China CDC, Beijing 100050, China.
Zhonghua Yi Xue Za Zhi. 2005 Nov 30;85(45):3181-5.
To investigate the single nucleotide polymorphism (SNP) of HIV-1 coreceptor CCR5 gene in Chinese Yi ethnic group and the association between these SNPs and HIV/AIDS.
Peripheral blood samples of 102 HIV negative persons of Chinese Yi nationality, 87 males amd 15 females, aged 23 (12-37), and 68 HIV carriers, 61 males and 7 females, aged 27 (17-51). The regulatory and structural regions of the HIV coreceptor CCR5 gene were amplified from the genomic DNA by nested PCR, each of the two regions was divided into three gene fragments which were overlapped. High throughput DHPLC was used for screening of unknown mutations in each gene fragment. The PCR products showing different peak traces from wild types in DHPLC were sequenced by forward and reverse primers respectively. The sequences were analyzed with the help of Sequence Navigator software to search for SNP loci. Statistical analysis by SPSS and PPAP softwares were made to study the association between these SNPs and HIV infection.
Five SNPs (A77G, G316A, T532C, C921T, and G668A) and a AGA deletion of the 686-688 nucleotides were discovered in the coding region of this gene in Chinese Yi ethnic group. C921T mutation was a nonsense mutation, and the other SNPs (A77G, G316A, T532C, and G668A) are sense mutation, with the amino acid changes of K26R, G106R, C178R, and R223Q. Only the frequency of R223Q allelic gene was high (0.08) but those of the others were low (less than 0.01). There was no significant difference in the allele frequency between the HIV negative and HIV positive groups (all P > 0.05). Five SNP loci (T58934G, G59029A, T59353C, G59402A, and C59653T) were found in the regulatory region of CCR5 gene with high allelic frequencies of 0.1912-0.2941. Between the HIV negative and HIV positive groups, there were no differences in the SNP loc (all P > 0.05). Statistical analysis of the association between the linkage of mutation loci with HIV infection suggested a significant difference in the haplotype frequency of T59353C-G59402A between the HIV negative and HIV positive groups of the Yi population.
A high throughput screening method of detecting unknown genetic mutation DHPLC can effectively analyze the SNP of CCR5 regulatory and structural regions in Chinese Yi ethnic group.
研究中国彝族人群人类免疫缺陷病毒1型(HIV-1)辅助受体CCR5基因的单核苷酸多态性(SNP)及其与HIV/AIDS的相关性。
选取102例彝族HIV阴性者外周血样本,男87例,女15例,年龄23(12 - 37)岁;68例HIV感染者外周血样本,男61例,女7例,年龄27(17 - 51)岁。采用巢式PCR从基因组DNA中扩增HIV辅助受体CCR5基因的调控区和结构区,将两个区域各分为3个相互重叠的基因片段。应用高通量变性高效液相色谱(DHPLC)技术对各基因片段进行未知突变筛查。对DHPLC中出现与野生型不同峰型的PCR产物分别用正反向引物进行测序。借助Sequence Navigator软件分析序列,寻找SNP位点。应用SPSS和PPAP软件进行统计分析,研究这些SNP与HIV感染的相关性。
在中国彝族人群该基因编码区发现5个SNP(A77G、G316A、T532C、C921T和G668A)以及686 - 688核苷酸处AGA缺失。C921T突变为无义突变,其他SNP(A77G、G316A、T532C和G668A)为错义突变,氨基酸改变分别为K26R、G106R、C178R和R223Q。仅R223Q等位基因频率较高(0.08),其他等位基因频率较低(小于0.01)。HIV阴性组与HIV阳性组等位基因频率差异无统计学意义(均P > 0.05)。在CCR5基因调控区发现5个SNP位点(T58934G、G59029A、T59353C、G59402A和C59653T),等位基因频率较高,为0.1912 - 0.2941。HIV阴性组与HIV阳性组间SNP位点差异无统计学意义(均P > 0.05)。对突变位点连锁与HIV感染相关性的统计分析表明,彝族人群HIV阴性组与HIV阳性组间T59353C - G59402A单倍型频率差异有统计学意义。
应用检测未知基因突变的高通量筛查方法DHPLC能有效分析中国彝族人群CCR5基因调控区和结构区的SNP。