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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Calcium kidney stones are associated with a haplotype of the calcium-sensing receptor gene regulatory region.
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Calcium kidney stones are associated with a haplotype of the calcium-sensing receptor gene regulatory region.

机译:钙肾结石与钙敏感受体基因调控区的单倍型有关。

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BACKGROUND: Calcium-sensing receptor gene (CaSR) is a candidate to explain susceptibility to calcium kidney stones. Thus, we studied CaSR gene single-nucleotide polymorphisms (SNPs) and haplotypes associated with stones. METHODS: Four hundred and sixty-three calcium stone formers and 213 healthy controls were genotyped for 21 SNPs mapping the whole CaSR gene. CaSR gene structure was studied. SNPs and haplotypes were analysed for association with stones. RESULTS: Three haplotype blocks were identified in the CaSR gene. The first block was characterized by six SNPs and included gene promoters. The rs7652589 and rs1501899 SNPs and the CATTCA haplotype of the first block were significantly more frequent in normocitraturic calcium kidney stone formers than controls. The risk of stones was increased in normocitraturic homozygous patients and heterozygotes for the CATTCA haplotype. The rate of stones was higher in stone formers with the CATTCA haplotype. In a three-generation family, calcium stones were associated with the CATTCA haplotype. The bioinformatic analysis identified a new site for the octamer-binding transcription factor 1 in the presence of the variant alleles at the rs7652589 and rs1501899 SNPs. This transcription factor may downregulate the transcription of vitamin D-dependent genes and the CaSR expression. Conclusion. SNPs and CATTCA haplotype of the CaSR gene first block is associated with kidney stones in normocitraturic patients.
机译:背景:钙敏感受体基因(CaSR)是解释钙肾结石敏感性的候选药物。因此,我们研究了CaSR基因单核苷酸多态性(SNPs)和与结石相关的单倍型。方法:对463个钙结石形成者和213名健康对照者进行基因分型,确定21个SNP位点,并绘制完整的CaSR基因。研究了CaSR基因的结构。分析了SNP和单倍型与结石的关系。结果:在CaSR基因中鉴定出三个单倍型区。第一个区块的特征是六个SNP,并包括基因启动子。在正常尿道钙化肾结石形成者中,rs7652589和rs1501899的SNP和CATTCA单元格的第一个区域明显比对照组更为频繁。 CATTCA单倍型的正常尿道纯合患者和杂合子患结石的风险增加。具有CATTCA单倍型的结石形成者的结石发生率更高。在三代家庭中,钙结石与CATTCA单倍型有关。生物信息学分析在rs7652589和rs1501899 SNP处存在变异等位基因时,确定了八聚体结合转录因子1的新位点。该转录因子可能下调维生素D依赖基因的转录和CaSR表达。结论。 CaSR基因第一个阻滞的SNP和CATTCA单倍型与正常尿道患者的肾结石有关。

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