Nephrology Research Group, Queens University Belfast, Belfast, Northern Ireland, UK.
J Hum Genet. 2010 Apr;55(4):248-51. doi: 10.1038/jhg.2010.15. Epub 2010 Mar 5.
Chemokine (C-C motif) ligand 5 (CCL5) and chemokine (C-C motif) receptor 5 are implicated in the pathogenesis of diabetic nephropathy (DN). We hypothesize that variants in these genes may be associated with DN. The CCL5 and chemokine receptor type 5 (CCR5) genes were resequenced, variants identified (n=58), allele frequencies determined in 46 individuals (92 chromosomes) and efficient haplotype tag single-nucleotide polymorphisms (htSNPs) selected to effectively evaluate the common variation in these genes. One reportedly functional gene variant and eight htSNPs were genotyped in a case-control association study involving Caucasian individuals with type 1 diabetes (267 cases with DN and 442 non-nephropathic diabetic controls). Genotyping was performed using MassARRAY iPLEX, TaqMan, gel electrophoresis and direct capillary sequencing. After correction for multiple testing, there were no statistically significant associations between variants in the CCL5 and CCR5 genes and DN.
趋化因子(C-C 基序)配体 5(CCL5)和趋化因子(C-C 基序)受体 5 参与糖尿病肾病(DN)的发病机制。我们假设这些基因中的变体可能与 DN 相关。对这些基因进行了重新测序,鉴定了变体(n=58),确定了 46 个人(92 条染色体)的等位基因频率,并选择了有效的单核苷酸多态性(htSNPs)来有效评估这些基因的常见变异。在一项涉及 1 型糖尿病个体的病例对照关联研究中,对一个报道的功能性基因变体和 8 个 htSNPs 进行了基因分型,该研究包括 267 例有 DN 的患者和 442 例非肾病性糖尿病对照者。使用 MassARRAY iPLEX、TaqMan、凝胶电泳和直接毛细管测序进行基因分型。在进行多次检验校正后,CCL5 和 CCR5 基因中的变体与 DN 之间没有统计学意义上的关联。