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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:人类全血中所选基因座上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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摘要

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 small tendency 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。关于个体间和性别特定的变异知之甚少。在这里,我们报告了96位健康的男性和96位健康的女性的总血中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,同时研究了单个位点的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。和在19q13.4(在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,两者的甲基化程度几乎相同,而甲基化程度较高的趋势很小在男性中。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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  • 来源
    《Human Genetics》 |2007年第5期|505-514|共10页
  • 作者单位

    Institute of Experimental Hematology and Transfusion Medicine University of Bonn Sigmund-Freud-Str. 25 53127 Bonn Germany;

    Institute of Experimental Hematology and Transfusion Medicine University of Bonn Sigmund-Freud-Str. 25 53127 Bonn Germany;

    Institute of Experimental Hematology and Transfusion Medicine University of Bonn Sigmund-Freud-Str. 25 53127 Bonn Germany;

    Institute of Experimental Hematology and Transfusion Medicine University of Bonn Sigmund-Freud-Str. 25 53127 Bonn Germany;

    Institute of Experimental Hematology and Transfusion Medicine University of Bonn Sigmund-Freud-Str. 25 53127 Bonn Germany;

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