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Measurements of DNA Methylation at Seven Loci in Various Tissues of CD1 Mice

机译:在CD1小鼠的各种组织DNa甲基化测量在七位点

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摘要

In humans, considerable variation in methylation at single loci and repetitive elements in various cells and tissues is observed. Recently, several inter- and intra-tissue correlations for DNA methylation have been reported. To investigate the extent and reproducibility of such correlations, we investigated inter- and intra-tissue methylation correlations among seven different loci in 9 different tissues in a population of 100 healthy seven-week-old CD1 outbred mice. We used a highly quantitative approach to measure methylation levels to high accuracy at two single loci in the alpha-actin and myosine light chain promoters, at three differentially methylated regions of the Peg3, Snrpn and Lit1 genes associated with imprinted loci, and at two repetitive elements in the Line-1 and IAP-LTR genes in the various tissues. In this population of mice, methylation at several loci was sex-associated and intra-tissue correlations among the studied loci were observed for brain and spleen. Inter-tissue correlations were rarely observed. To investigate method-dependent experimental variability, we re-analyzed the same spleen and tongue samples using SIRPH and pyrosequencing methods and reconfirmed intra-tissue correlations for spleen and sex-associated correlations for DNA methylation for tongue. When we repeated DNA methylation measurements for a second mouse population raised under similar conditions three months later, we did not detect sex-associated or intra-tissues correlations. Additional studies that examine large numbers of loci may be required to further understand the factors that influence stability of DNA methylation.
机译:在人类中,在各种细胞和组织中的单个位点处的甲基化和重复元件的甲基化变化都很大。最近,已经报道了几种组织间和组织内DNA甲基化的相关性。为了研究此类相关性的程度和可重复性,我们研究了100只健康的7周龄CD1近交小鼠群体中9个不同组织中七个不同基因座之间的组织间和组织内甲基化相关性。我们使用高度定量的方法在α-肌动蛋白和肌苷轻链启动子中的两个单个基因座,与印迹基因座相关的Peg3,Snrpn和Lit1基因的三个差异甲基化区域以及两个重复的基因组中,高精度地测量甲基化水平。各种组织中Line-1和IAP-LTR基因中的元素。在这群小鼠中,几个基因座处的甲基化与性别相关,并且在研究的基因座之间的组织内相关性被观察到为大脑和脾脏。很少观察到组织间的相关性。为了研究依赖方法的实验变异性,我们使用SIRPH和焦磷酸测序方法重新分析了相同的脾脏和舌头样本,并确认了脾脏的组织内相关性和舌头DNA甲基化的性别相关性。三个月后,当我们对在相似条件下饲养的第二只小鼠群体重复进行DNA甲基化测量时,我们没有检测到性别相关或组织内相关性。可能需要进行其他研究,检查大量基因座,以进一步了解影响DNA甲基化稳定性的因素。

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