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SLC22A12基因第8外显子和第8内含子多态与中国汉族人原发性高尿酸血症关联研究
引用本文:孟冬梅,韩琳,苗志敏,李长贵. SLC22A12基因第8外显子和第8内含子多态与中国汉族人原发性高尿酸血症关联研究[J]. 中华医学遗传学杂志, 2010, 27(6). DOI: 10.3760/cma.j.issn.1003-9406.2010.06.012
作者姓名:孟冬梅  韩琳  苗志敏  李长贵
摘    要:目的 研究原发性高尿酸血症患者SLC22AI2基因第8内含子和第8外显子单核苷酸多态(single nucleotide polymorphism,SNP)位点与原发性高尿酸血症遗传易感性的关系.方法 选择山东沿海地区原发性高尿酸血症患者215例,正常对照人群323名.提取基因组DNA,PCR扩增SLC22A12基因第8内含子和第8外显子,对PCR扩增产物进行测序.结果 序列分析发现:(1)SLC22AI2基因第8外显子存在T1309C单核苷酸多态,第8内含子存在-103A>G单核苷酸多态,这2个多态位点完全连锁.(2)高尿酸血症组-103A>G G等位基因频率和T1309C C等位基因频率明显高于正常对照组(均为51.9%vs.42.4%,P<0.01);(3)高尿酸血症组GG+GA基因型频率和CC+CT基因型频率显著高于正常对照组(均为80.0%vs.69.0%,P<0.01).(4)-103 A>G和T1309C基因多态中,含有等位基因G的基因型GG+GA及含有等位基因C的基因型CC+CT均使高尿酸血症的发病危险性上升了1.79倍(OR=1.79,95%CI:1.19~2.70).结论 SLC22A12基因第8外显子T130gC及第8内含子-103A>G SNP与原发性高尿酸血症密切相关.

关 键 词:原发性高尿酸血症  SLC22A12基因  单核苷酸多态性

Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population
MENG Dong-mei,HAN Lin,MIAO Zhi-min,LI Chang-gui. Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population[J]. Chinese journal of medical genetics, 2010, 27(6). DOI: 10.3760/cma.j.issn.1003-9406.2010.06.012
Authors:MENG Dong-mei  HAN Lin  MIAO Zhi-min  LI Chang-gui
Abstract:Objective To investigate the association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene SLC22A12 with primary hyperuricemia (HUA) in Chinese Han population.Methods Genomic DNA from 215 individuals with HUA and 323 controls was extracted. The exon 8 and intron 8 of the SLC22A12 gene was amplified by polymerase chain reaction (PCR). PCR product was sequenced directly. Single nucleotide polymorphisms (SNPs) were detected and the association of the SNPs with primary HUA was assessed. Results (1) Two SNPs were identified, they were T1309C located in exon 8 (rs7932775) and -103A>G located in intron 8. Pairwise linkage disequilibrium analysis displayed an absolute linkage disequilibrium between the two SNPs (D'= 1). (2) The minor allele frequencies for both SNPs were 51.9 % in HUA patients, which were significantly different from that of controls (42.4 % ) (P<0.01). (3) The genotype frequencies of GG + GA and CC + CT in HUA patients were significantly higher than that in controls (80. 0% vs. 69.0%,P<0. 01). (4) Individuals of both GG+GA and CC+CT genotypes had 1.79 fold increase of HUA risk (OR = 1.794,95% CI:1.19-2.70). Conclusion These findings indicated that T1309C and -103A>G polymorphisms of the SLC22A12 gene were associated with primary HUA in Chinese Han population.
Keywords:primary hyperuricemia  SLC22A12 gene  single nucleotide polymorphism
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