Annotation of chromatin states in 66 complete mouse epigenomes during development.

Autor: van der Velde A; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA.; Bioinformatics Program, Boston University, Boston, MA, 02215, USA., Fan K; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA., Tsuji J; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA., Moore JE; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA., Purcaro MJ; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA., Pratt HE; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA., Weng Z; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, MA, USA. zhiping.weng@umassmed.edu.
Jazyk: angličtina
Zdroj: Communications biology [Commun Biol] 2021 Feb 22; Vol. 4 (1), pp. 239. Date of Electronic Publication: 2021 Feb 22.
DOI: 10.1038/s42003-021-01756-4
Abstrakt: The morphologically and functionally distinct cell types of a multicellular organism are maintained by their unique epigenomes and gene expression programs. Phase III of the ENCODE Project profiled 66 mouse epigenomes across twelve tissues at daily intervals from embryonic day 11.5 to birth. Applying the ChromHMM algorithm to these epigenomes, we annotated eighteen chromatin states with characteristics of promoters, enhancers, transcribed regions, repressed regions, and quiescent regions. Our integrative analyses delineate the tissue specificity and developmental trajectory of the loci in these chromatin states. Approximately 0.3% of each epigenome is assigned to a bivalent chromatin state, which harbors both active marks and the repressive mark H3K27me3. Highly evolutionarily conserved, these loci are enriched in silencers bound by polycomb repressive complex proteins, and the transcription start sites of their silenced target genes. This collection of chromatin state assignments provides a useful resource for studying mammalian development.
Databáze: MEDLINE
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