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Occupancy maps of 208 chromatin-associated proteins in one human cell type
Transcription factors are DNA-binding proteins that have key roles in gene regulation(1,2). Genome-wide occupancy maps of transcriptional regulators are important for understanding gene regulation and its effects on diverse biological processes(3–6). However, only a minority of the more than 1,600 t...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398277/ https://www.ncbi.nlm.nih.gov/pubmed/32728244 http://dx.doi.org/10.1038/s41586-020-2023-4 |
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author | Partridge, E. Christopher Chhetri, Surya B. Prokop, Jeremy W. Ramaker, Ryne C. Jansen, Camden S. Goh, Say-Tar Mackiewicz, Mark Newberry, Kimberly M. Brandsmeier, Laurel A. Meadows, Sarah K. Messer, C. Luke Hardigan, Andrew A. Coppola, Candice J. Dean, Emma C. Jiang, Shan Savic, Daniel Mortazavi, Ali Wold, Barbara J. Myers, Richard M. Mendenhall, Eric M. |
author_facet | Partridge, E. Christopher Chhetri, Surya B. Prokop, Jeremy W. Ramaker, Ryne C. Jansen, Camden S. Goh, Say-Tar Mackiewicz, Mark Newberry, Kimberly M. Brandsmeier, Laurel A. Meadows, Sarah K. Messer, C. Luke Hardigan, Andrew A. Coppola, Candice J. Dean, Emma C. Jiang, Shan Savic, Daniel Mortazavi, Ali Wold, Barbara J. Myers, Richard M. Mendenhall, Eric M. |
author_sort | Partridge, E. Christopher |
collection | PubMed |
description | Transcription factors are DNA-binding proteins that have key roles in gene regulation(1,2). Genome-wide occupancy maps of transcriptional regulators are important for understanding gene regulation and its effects on diverse biological processes(3–6). However, only a minority of the more than 1,600 transcription factors encoded in the human genome has been assayed. Here we present, as part of the ENCODE (Encyclopedia of DNA Elements) project, data and analyses from chromatin immunoprecipitation followed by high-throughput sequencing (ChIP–seq) experiments using the human HepG2 cell line for 208 chromatin-associated proteins (CAPs). These comprise 171 transcription factors and 37 transcriptional cofactors and chromatin regulator proteins, and represent nearly one-quarter of CAPs expressed in HepG2 cells. The binding profiles of these CAPs form major groups associated predominantly with promoters or enhancers, or with both. We confirm and expand the current catalogue of DNA sequence motifs for transcription factors, and describe motifs that correspond to other transcription factors that are co-enriched with the primary ChIP target. For example, FOX family motifs are enriched in ChIP–seq peaks of 37 other CAPs. We show that motif content and occupancy patterns can distinguish between promoters and enhancers. This catalogue reveals high-occupancy target regions at which many CAPs associate, although each contains motifs for only a minority of the numerous associated transcription factors. These analyses provide a more complete overview of the gene regulatory networks that define this cell type, and demonstrate the usefulness of the large-scale production efforts of the ENCODE Consortium. |
format | Online Article Text |
id | pubmed-7398277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73982772020-08-17 Occupancy maps of 208 chromatin-associated proteins in one human cell type Partridge, E. Christopher Chhetri, Surya B. Prokop, Jeremy W. Ramaker, Ryne C. Jansen, Camden S. Goh, Say-Tar Mackiewicz, Mark Newberry, Kimberly M. Brandsmeier, Laurel A. Meadows, Sarah K. Messer, C. Luke Hardigan, Andrew A. Coppola, Candice J. Dean, Emma C. Jiang, Shan Savic, Daniel Mortazavi, Ali Wold, Barbara J. Myers, Richard M. Mendenhall, Eric M. Nature Article Transcription factors are DNA-binding proteins that have key roles in gene regulation(1,2). Genome-wide occupancy maps of transcriptional regulators are important for understanding gene regulation and its effects on diverse biological processes(3–6). However, only a minority of the more than 1,600 transcription factors encoded in the human genome has been assayed. Here we present, as part of the ENCODE (Encyclopedia of DNA Elements) project, data and analyses from chromatin immunoprecipitation followed by high-throughput sequencing (ChIP–seq) experiments using the human HepG2 cell line for 208 chromatin-associated proteins (CAPs). These comprise 171 transcription factors and 37 transcriptional cofactors and chromatin regulator proteins, and represent nearly one-quarter of CAPs expressed in HepG2 cells. The binding profiles of these CAPs form major groups associated predominantly with promoters or enhancers, or with both. We confirm and expand the current catalogue of DNA sequence motifs for transcription factors, and describe motifs that correspond to other transcription factors that are co-enriched with the primary ChIP target. For example, FOX family motifs are enriched in ChIP–seq peaks of 37 other CAPs. We show that motif content and occupancy patterns can distinguish between promoters and enhancers. This catalogue reveals high-occupancy target regions at which many CAPs associate, although each contains motifs for only a minority of the numerous associated transcription factors. These analyses provide a more complete overview of the gene regulatory networks that define this cell type, and demonstrate the usefulness of the large-scale production efforts of the ENCODE Consortium. Nature Publishing Group UK 2020-07-29 2020 /pmc/articles/PMC7398277/ /pubmed/32728244 http://dx.doi.org/10.1038/s41586-020-2023-4 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Partridge, E. Christopher Chhetri, Surya B. Prokop, Jeremy W. Ramaker, Ryne C. Jansen, Camden S. Goh, Say-Tar Mackiewicz, Mark Newberry, Kimberly M. Brandsmeier, Laurel A. Meadows, Sarah K. Messer, C. Luke Hardigan, Andrew A. Coppola, Candice J. Dean, Emma C. Jiang, Shan Savic, Daniel Mortazavi, Ali Wold, Barbara J. Myers, Richard M. Mendenhall, Eric M. Occupancy maps of 208 chromatin-associated proteins in one human cell type |
title | Occupancy maps of 208 chromatin-associated proteins in one human cell type |
title_full | Occupancy maps of 208 chromatin-associated proteins in one human cell type |
title_fullStr | Occupancy maps of 208 chromatin-associated proteins in one human cell type |
title_full_unstemmed | Occupancy maps of 208 chromatin-associated proteins in one human cell type |
title_short | Occupancy maps of 208 chromatin-associated proteins in one human cell type |
title_sort | occupancy maps of 208 chromatin-associated proteins in one human cell type |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398277/ https://www.ncbi.nlm.nih.gov/pubmed/32728244 http://dx.doi.org/10.1038/s41586-020-2023-4 |
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