期刊
NATURE
卷 480, 期 7378, 页码 490-495出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nature10716
关键词
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资金
- EMBO
- Marie Curie International Incoming fellowship
- Novartis Research Foundation
- European Union (NoE) [FP7-HEALTH-2010-257082]
- European Research Council (ERC EpiGePlas)
- SNF
- Swiss initiative in Systems Biology
Methylation of cytosines is an essential epigenetic modification in mammalian genomes, yet the rules that govern methylation patterns remain largely elusive. To gain insights into this process, we generated base-pair-resolution mouse methylomes in stem cells and neuronal progenitors. Advanced quantitative analysis identified low-methylated regions (LMRs) with an average methylation of 30%. These represent CpG-poor distal regulatory regions as evidenced by location, DNase I hypersensitivity, presence of enhancer chromatin marks and enhancer activity in reporter assays. LMRs are occupied by DNA-binding factors and their binding is necessary and sufficient to create LMRs. A comparison of neuronal and stem-cell methylomes confirms this dependency, as cell-type-specific LMRs are occupied by cell-type-specific transcription factors. This study provides methylome references for the mouse and shows that DNA-binding factors locally influence DNA methylation, enabling the identification of active regulatory regions.
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