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MBD-isolated Genome Sequencing provides a high-throughput and comprehensive survey of DNA methylation in the human genome

机译:MBD分离的基因组测序可对人类基因组中的DNA甲基化进行高通量全面的研究

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DNA methylation is an epigenetic modification involved in both normal developmental processes and disease states through the modulation of gene expression and the maintenance of genomic organization. Conventional methods of DNA methylation analysis, such as bisulfite sequencing, methylation sensitive restriction enzyme digestion and array-based detection techniques, have major limitations that impede high-throughput genome-wide analysis. We describe a novel technique, MBD-isolated Genome Sequencing (MiGS), which combines precipitation of methylated DNA by recombinant methyl-CpG binding domain of MBD2 protein and sequencing of the isolated DNA by a massively parallel sequencer. We utilized MiGS to study three isogenic cancer cell lines with varying degrees of DNA methylation. We successfully detected previously known methylated regions in these cells and identified hundreds of novel methylated regions. This technique is highly specific and sensitive and can be applied to any biological settings to identify differentially methylated regions at the genomic scale.
机译:DNA甲基化是一种通过调节基因表达和维持基因组组织而参与正常发育过程和疾病状态的表观遗传修饰。常规的DNA甲基化分析方法,如亚硫酸氢盐测序,甲基化敏感的限制性酶切消化和基于阵列的检测技术,具有主要的局限性,阻碍了高通量全基因组分析。我们描述了一种新技术,MBD分离的基因组测序(MiGS),它结合了MBD2蛋白的重组甲基CpG结合域对甲基化DNA的沉淀,并通过大规模平行测序仪对分离的DNA进行了测序。我们利用MiGS研究了三种具有不同DNA甲基化程度的同基因癌细胞系。我们成功地检测了这些细胞中以前已知的甲基化区域,并鉴定了数百个新的甲基化区域。该技术是高度特异性和灵敏的,可应用于任何生物学环境,以鉴定基因组规模上的差异甲基化区域。

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