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首页> 外文期刊>BMC Medical Genomics >Comparison of DNA methylation profiles from saliva in Coeliac disease and non-coeliac disease individuals
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Comparison of DNA methylation profiles from saliva in Coeliac disease and non-coeliac disease individuals

机译:乳糜泻和非乳糜泻唾液中DNA甲基化谱的比较

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摘要

Coeliac disease (CD) is a autoimmune disease characterised by mucosal inflammation in the small intestine in response to dietary gluten. Genetic factors play a key role with CD individuals carrying either the HLA-DQ2 or HLA-DQ8 haplotype, however these haplotypes are present in half the general population making them necessary but insufficient to cause CD. Epigenetic modifications, including DNA methylation that can change in response to environmental exposure could help to explain how interactions between genes and environmental factors combine to trigger disease development. Identifying changes in DNA methylation profiles in individuals with CD could help discover novel genomic regions involved in the onset and development of CD. The Illumina InfiniumMethylation450 Beadchip array (HM450) was used to compare DNA methylation profiles in saliva, in CD and non-CD affected individuals. CD individuals who had been diagnosed at least 2?years previously; were on a GFD; and who were currently asymptomatic; were compared to age and sex-matched non-CD affected healthy controls. Bisulphite pyrosequencing was used to validate regions found to be differentially methylated. These regions were also validated in a second larger cohort of CD and non-CD affected individuals. Methylation differences within the HLA region at HLA-DQB1 were identified on HM450 but could not be confirmed with pyrosequencing. Significant methylation differences near the SLC17A3 gene were confirmed on pyrosequencing in the initial pilot cohort. Interestingly pyrosequencing sequencing of these same sites within a second cohort of CD and non-CD affected controls produced significant methylation differences in the opposite direction. Altered DNA methylation profiles appear to be present in saliva in CD individuals. Further work to confirm whether these differences are truly associated with CD is needed.
机译:乳糜泻(CD)是一种自身免疫性疾病,其特征在于小肠中的粘膜炎症,响应膳食麸质。遗传因素在携带HLA-DQ2或HLA-DQ8单倍型的CD个体发挥关键作用,但这些单倍型在一般人群中存在,使其必要但不足以引起CD。表观遗传修饰,包括可以改变环境暴露的DNA甲基化可以有助于解释基因与环境因素之间的相互作用如何结合引发疾病发展。鉴定CD中的个体中DNA甲基化谱的变化可以帮助发现参与CD发作和发育的新型基因组区域。 Illumina Infinium甲基化450珠芯片阵列(HM450)用于将DNA甲基化曲线与CD和非Cd受影响的个体进行比较。诊断为至少2年的CD个体以前诊断出来;在GFD上;谁是目前无症状的;与年龄和性匹配的非CD影响健康对照进行比较。双硫酸氢淀粉术用于验证发现差异甲基化的区域。这些区域也以第二个较大的CD和非CD受影响的个体验证。在HM450上鉴定HLA-DQB1的HLA区域内的甲基化差异,但不能用焦磷酸测序证实。在最初的先导队队列中,证实了SLC17A3基因附近的显着甲基化差异。有趣的是,在第二次CD和非Cd受影响对照中,这些相同的位点测序这些相同的位点在相反方向上产生了显着的甲基化差异。改变的DNA甲基化曲线似乎存在于CD个体中的唾液中。进一步的工作以确认这些差异是否真正与CD相关联。

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