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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
来源:
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.
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页码:695 / 706
页数:12
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