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首页> 外文期刊>Clinical epigenetics. >Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects
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Mendelian inheritance of trimodal CpG methylation sites suggests distal cis-acting genetic effects

机译:孟德尔遗传的三峰CpG甲基化位点提示远端顺式作用遗传效应

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class="Heading">Background id="Par1" class="Para">Environmentally influenced phenotypes, such as obesity and insulin resistance, can be transmitted over multiple generations. Epigenetic modifications, such as methylation of DNA cytosine-guanine (CpG) pairs, may be carriers of inherited information. At the population level, the methylation state of such a€?heritablea€? CpG sites is expected to follow a trimodal distribution, and their mode of inheritance should be Mendelian. class="Heading">Methods id="Par2" class="Para">Using the Illumina Infinium 450??K DNA methylation array, we determined DNA CpG-methylation in blood cells from a family cohort 123 individuals of Arab ethnicity, including 18 elementary father-mother-child trios, we asked whether Mendelian inheritance of CpG methylation is observed, and most importantly, whether it is independent of any genetic signals. Using 40?— whole genome sequencing, we therefore excluded all CpG sites with possibly confounding genetic variants (SNP) within the binding regions of the Illumina probes. class="Heading">Results id="Par3" class="Para">We identified a total of 955 CpG sites that displayed a trimodal distribution and confirmed trimodality in a study of 1805 unrelated Caucasians. Of 955 CpG sites, 99.9% observed a strict Mendelian pattern of inheritance and had no SNP within +/a?’110 nucleotides of the CpG site by design. However, in 97% of these cases a distal cis-acting SNP within a +/a?’1??Mbp window was found that explained the observed CpG distribution, excluding the hypothesis of epigenetic inheritance for these clear-cut trimodal sites. Using power analysis, we showed that in 46% of all cases, the closest CpG-associated SNP was located more than 1000??bp from the CpG site. class="Heading">Conclusions id="Par4" class="Para">Our findings suggest that CpG methylation is maintained over larger genomic distances. Furthermore, nearly half of the SNPs associated with these trimodal sites were also associated with the expression of nearby genes (Pa€‰=a€‰4.08a€‰?—a€‰10a?’6), implying a regulatory effect of these trimodal CpG sites.
机译:class =“ Heading”>背景 id =“ Par1” class =“ Para”>受环境影响的表型(例如肥胖症和胰岛素抵抗)可以多代传播。表观遗传修饰,例如DNA胞嘧啶-鸟嘌呤(CpG)对的甲基化,可能是遗传信息的载体。在人口一级,这种“可遗传性”的甲基化状态。 CpG网站应遵循三峰分布,其继承方式应为孟德尔式。 class =“ Heading”>方法 id =“ Par2” class =“ Para”>使用在Illumina Infinium 450 ?? K DNA甲基化阵列中,我们确定了来自123个阿拉伯族的一个家庭队列(包括18个基本的父子三重奏)的血细胞中的DNA CpG-甲基化,我们询问是否观察到孟德尔遗传的CpG甲基化,最重要的是,它是否独立于任何遗传信号。因此,使用40个全基因组测序,我们排除了Illumina探针结合区内所有可能具有混淆性遗传变异(SNP)的CpG位点。 class =“ Heading”>结果 id =“ Par3” class =“ Para”>在对1805位无关的高加索人的研究中,我们确定了总共955个CpG站点,这些站点显示了三峰分布并确认了三峰分布。根据设计,在955个CpG位点中,有99.9%的人观察到严格的孟德尔遗传模式,并且在CpG位点的+/- 110个核苷酸内没有SNP。然而,在这些病例的97%中,发现在+ / a?1?Mbp窗口内有一个远端顺式作用SNP,解释了观察到的CpG分布,但排除了这些明确的三峰位点表观遗传的假设。使用功效分析,我们发现在所有病例中,有46%的患者与CpG相关的SNP距离CpG位点均超过1000?bp。 class =“ Heading”>结论 id =“ Par4” class =“ Para”>我们的发现表明CpG甲基化在较大的基因组距离内得以维持。此外,与这些三峰位点相关的SNP几乎有一半也与附近基因的表达相关( P a = 4.08a ?? ‰10 a?'6 ),暗示了这些三峰CpG位点的调节作用。

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