MIRA-seq for DNA methylation analysis of CpG islands

被引:24
|
作者
Jung, Marc [1 ]
Kadam, Swati [1 ]
Xiong, Wenying [1 ]
Rauch, Tibor A. [2 ]
Jin, Seung-Gi [1 ,3 ]
Pfeifer, Gerd P. [1 ,3 ]
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Duarte, CA 91010 USA
[2] Rush Univ, Med Ctr, Dept Orthoped Surg, Chicago, IL 60612 USA
[3] Van Andel Res Inst, Grand Rapids, MI 49503 USA
关键词
CpG islands; DNA methylation; high-throughput sequencing; methyl-CpG-binding protein; methylated-CpG island recovery assay; LUNG-CANCER; TRANSCRIPTIONAL REPRESSOR; BINDING-PROTEINS; RECOVERY ASSAY; GENOME; IDENTIFICATION; CELLS; WIDE; RESOLUTION; METHYLOME;
D O I
10.2217/epi.15.33
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To develop a reliable method for whole genome analysis of DNA methylation. Materials & methods: Genome-scale analysis of DNA methylation includes affinity-based approaches such as enrichment using methyl-CpG-binding proteins. One of these methods, the methylated-CpG island recovery assay (MIRA), is based on the high affinity of the MBD2b-MBD3L1 complex for CpG-methylated DNA. Here we provide a detailed description of MIRA and combine it with next generation sequencing platforms (MIRA-seq). Results: We assessed the performance of MIRA-seq and compared the data with whole genome bisulfite sequencing. Conclusion: MIRA-seq is a reliable, genome-scale DNA methylation analysis platform for scoring DNA methylation differences at CpG-rich genomic regions. The method is not limited by primer or probe design and is cost effective.
引用
收藏
页码:695 / 706
页数:12
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