DNA Methylome Analysis Identifies Transcription Factor-Based Epigenomic Signatures of Multilineage Competence in Neural Stem/Progenitor Cells
Epigenomics
DNA demethylation
Epigenome
DOI:
10.1016/j.celrep.2017.08.086
Publication Date:
2017-09-19T23:16:36Z
AUTHORS (11)
ABSTRACT
Regulation of the epigenome during in vivo specification brain stem cells is still poorly understood. Here, we report DNA methylome analyses directly sampled cortical neural and progenitor (NS/PCs) at different development stages, as well those terminally differentiated neurons, astrocytes, oligodendrocytes. We found that sequential NS/PCs regulated by two successive waves demethylation early late which are responsible for establishment neuron- glia-specific low-methylated regions (LMRs), respectively. The regulatory role gliogenic genes was substantiated enrichment nuclear factor I (NFI)-binding sites. provide evidence de novo methylation neuron-specific LMRs establishes epigenotypes, essentially silencing neuronal genes. Our data highlight implications dynamics shaping epigenomic features confer differentiation potential sequentially development.
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