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Effect of genetic polymorphisms in ca6 gene on the expression and catalytic activity of human salivary carbonic anhydrase VI

机译:ca6基因多态性对人唾液碳酸酐酶VI表达和催化活性的影响

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Carbonic anhydrase isoenzyme VI (CA VI) plays an important role in the homeostasis of oral tissues participating in the processes of taste, protection of dental tissues against the loss of minerals, caries, and possibly in the formation of dental calculus in periodontal disease. This study aimed to verify the correlation between changes in the expression and activity of human salivary carbonic anhydrase VI and genetic polymorphisms in its gene (CA6). The study population consisted of 182 healthy volunteers (female and male, aged 18-22). Samples of total saliva were assayed for CA VI concentrations using a specific time-resolved immunofluorometric assay. CA VI catalytic activity was detected by a modified protocol of Kotwica et al. [J Physiol Pharmacol 2006;57(suppl 8):107-123], adapted to CA VI in saliva. Samples of genomic DNA were genotyped for polymorphisms rs2274327 (C/T), rs2274328 (A/C) and rs2274333 (A/G) by TaqMan? SNP Genotyping Assays. The concentration and catalytic activity of the salivary CA VI obtained for the different genotypes were analyzed using the Kruskal-Wallis nonparametric test and the Dunn test. The results showed that individuals with TT genotype (rs2274327) had significantly lower CA VI concentrations than the individuals with genotypes CT or CC (p < 0.05). There was also an association between polymorphism rs2274333 and salivary CA VI concentrations. There were no associations between the three polymorphisms analyzed and variations in CA VI activity. Our results suggest that polymorphisms in the CA6 gene are associated with the concentrations of secreted CA VI.
机译:碳酸酐酶同工酶VI(CA VI)在参与味觉过程的口腔组织的稳态,保护牙齿组织免受矿物质,龋齿的损失以及可能在牙周疾病中形成牙结石方面起着重要作用。这项研究旨在验证人类唾液碳酸酐酶VI表达和活性的变化与其基因(CA6)的遗传多态性之间的相关性。研究人群包括182名健康志愿者(男女,年龄在18-22岁之间)。使用特定的时间分辨免疫荧光测定法分析总唾液样本中的CA VI浓度。通过Kotwica等人的改进方案检测CA VI催化活性。 [J Physiol Pharmacol 2006; 57(suppl 8):107-123],适用于唾液中的CA VI。通过TaqMan?对基因组DNA样本进行rs2274327(C / T),rs2274328(A / C)和rs2274333(A / G)多态性的基因分型。 SNP基因分型分析。使用Kruskal-Wallis非参数检验和Dunn检验分析了不同基因型获得的唾液CA VI的浓度和催化活性。结果表明,TT基因型个体(rs2274327)的CA VI浓度明显低于CT或CC基因型个体(p <0.05)。 rs2274333多态性与唾液CA VI浓度之间也存在关联。分析的三种多态性与CA VI活性的变化之间没有关联。我们的结果表明,CA6基因的多态性与分泌的CA VI的浓度有关。

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