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Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males.

机译:从人类全血中选择的基因座处,DNA甲基化水平的性别特异性差异:男性中甲基化水平较高的趋势。

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Abnormal patterns of DNA methylation are observed in many diseases such as tumors and imprinting disorders. Little is known about inter-individual and gender specific variations. Here, we report on accurate and sensitive quantitative measurements of methylation in DNA from total blood in 96 healthy human males and 96 healthy human females. Global methylation was estimated by studying two repetitive DNA elements, namely Line-1 and Alu repeats, while single loci were investigated for three differentially methylated regions (DMRs) at PEG3, NESP55 and H19 imprinted genes and two additional loci at Xq28 (F8 gene) and at 19q13.4 (locus between PEG3 and ubiquitin specific protease 29). We observed inter-individual correlations in the degree of methylation between Alu and Line-1 repeats. Moreover, all studied CpGs showed slightly higher methylation in males (P < 0.0003-0.0381), with the exception of DMRs at imprinted genes (P = 0.0342-0.9616) which were almost equally methylated in both sexes with only a smalltendency towards higher methylation in males. This observed difference could be due to the process of X chromosome inactivation or merely to the presence of an additional X chromosome in female cells or could be a result of downstream effects of sex determination.
机译:在许多疾病(例如肿瘤和印迹疾病)中观察到DNA甲基化的异常模式。关于个体之间和性别的差异知之甚少。在这里,我们报告了96位健康的男性和96位健康的女性的全血中DNA甲基化的准确和灵敏的定量测量。通过研究两个重复的DNA元素(即Line-1和Alu重复序列)来估算总体甲基化,同时研究了单个基因座的PEG3,NESP55和H19印迹基因的三个差异甲基化区域(DMR)和Xq28(F8基因)的两个附加基因座。并且在19q13.4处(PEG3和泛素特异性蛋白酶29之间的位置)。我们观察到Alu和Line-1重复序列之间甲基化程度的个体间相关性。此外,所有研究的CpGs均显示出男性的甲基化程度略高(P <0.0003-0.0381),但印记基因的DMRs(P = 0.0342-0.9616)除外,这两个性别的甲基化程度几乎相同,而在较高的甲基化水平下则偏小。男性。这种观察到的差异可能是由于X染色体失活的过程,或者仅仅是女性细胞中存在额外的X染色体,或者是性别决定的下游效应的结果。

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