Annotation of chromatin states in 66 complete mouse epigenomes during development
dc.contributor.author | van der Velde, Arjan | |
dc.contributor.author | Fan, Kaili | |
dc.contributor.author | Tsuji, Junko | |
dc.contributor.author | Moore, Jill E. | |
dc.contributor.author | Purcaro, Michael J. | |
dc.contributor.author | Pratt, Henry E. | |
dc.contributor.author | Weng, Zhiping | |
dc.date | 2022-08-11T08:09:59.000 | |
dc.date.accessioned | 2022-08-23T16:51:05Z | |
dc.date.available | 2022-08-23T16:51:05Z | |
dc.date.issued | 2021-02-22 | |
dc.date.submitted | 2021-05-05 | |
dc.identifier.citation | <p>van der Velde A, Fan K, Tsuji J, Moore JE, Purcaro MJ, Pratt HE, Weng Z. Annotation of chromatin states in 66 complete mouse epigenomes during development. Commun Biol. 2021 Feb 22;4(1):239. doi: 10.1038/s42003-021-01756-4. PMID: 33619351; PMCID: PMC7900196. <a href="https://doi.org/10.1038/s42003-021-01756-4">Link to article on publisher's site</a></p> | |
dc.identifier.issn | 2399-3642 (Linking) | |
dc.identifier.doi | 10.1038/s42003-021-01756-4 | |
dc.identifier.pmid | 33619351 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/41791 | |
dc.description.abstract | 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. | |
dc.language.iso | en_US | |
dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=33619351&dopt=Abstract">Link to Article in PubMed</a></p> | |
dc.rights | Copyright © The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Epigenetic memory | |
dc.subject | Genome informatics | |
dc.subject | Epigenomics | |
dc.subject | Gene regulation | |
dc.subject | Cell Biology | |
dc.subject | Developmental Biology | |
dc.subject | Genomics | |
dc.subject | Integrative Biology | |
dc.title | Annotation of chromatin states in 66 complete mouse epigenomes during development | |
dc.type | Journal Article | |
dc.source.journaltitle | Communications biology | |
dc.source.volume | 4 | |
dc.source.issue | 1 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5623&context=oapubs&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/4591 | |
dc.identifier.contextkey | 22797289 | |
refterms.dateFOA | 2022-08-23T16:51:05Z | |
html.description.abstract | <p>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.</p> | |
dc.identifier.submissionpath | oapubs/4591 | |
dc.contributor.department | Graduate School of Biomedical Sciences | |
dc.contributor.department | Program in Bioinformatics and Integrative Biology | |
dc.source.pages | 239 |