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Role of TRAV locus in low caries experience

机译:TRAV基因座在低龋经验中的作用

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Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27. In the present study, we fine mapped the 14q11.2 locus to identify genetic contributors to caries susceptibility. Four hundred seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. An additional 387 DNA samples from unrelated individuals were used to determine allele frequencies. For replication purposes, a total of 1,446 independent subjects from four different populations were analyzed based on their caries experience (low versus high). Forty-eight markers in 14q11.2 were genotyped using TaqMan chemistry. Transmission disequilibrium test was used to detect over transmission of alleles in the Filipino families, and Chi-square, Fisher's exact and logistic regression were used to test for association between low caries experience and variant alleles in the replication data sets. We finally assessed the mRNA expression of TRAV4 in the saliva of 143 study subjects. In the Filipino families, statistically significant associations were found between low caries experience and markers in TRAV4. We were able to replicate these results in the populations studied that were characteristically from underserved areas. Direct sequencing of 22 subjects carrying the associated alleles detects one missense mutation (Y30R) that is predicted to be probably damaging. Finally, we observed higher expression in children and teenagers with low caries experience, correlating with specific alleles in TRAV4. Our results suggest that TRAV4 may have a role in protecting against caries.
机译:龋病是当今世界上最常见的慢性多因素疾病。影响遗传易感性的遗传因素还知之甚少。我们之前的全基因组连锁扫描已确定了与龋齿易感性相关的五个基因座:5q13.3、13q31.1、14q11.2、14q 24.3和Xq27。在本研究中,我们对14q11.2基因座进行了精细定位,以鉴定导致龋齿易感性的遗传因素。研究了来自72个家谱的477名受试者,他们具有相似的文化和行为习惯,并且在菲律宾居住的牙齿保健服务有限。来自无关个体的另外387个DNA样品被用于确定等位基因频率。为了复制的目的,根据龋病经验(低与高)对来自四个不同人群的总共1,446位独立受试者进行了分析。使用TaqMan化学对14q11.2中的48个标记进行基因分型。传播不平衡测试用于检测菲律宾家庭中等位基因的过度传播,卡方检验,Fisher精确和逻辑回归用于检验低龋病经验与复制数据集中的变异等位基因之间的关联。我们最终评估了143位研究对象唾液中TRAV4的mRNA表达。在菲律宾家庭中,低龋经验与TRAV4中的标记物之间存在统计学上的显着关联。我们能够在服务不足地区特有的人口研究中复制这些结果。对携带相关等位基因的22位受试者进行直接测序可检测到一种可能会造成破坏的错义突变(Y30R)。最后,我们观察到在龋病少的儿童和青少年中有较高的表达,与TRAV4中的特定等位基因相关。我们的结果表明,TRAV4可能在预防龋齿中起作用。

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