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Broad genic repression domains signify enhanced silencing of oncogenes
Cancers result from a set of genetic and epigenetic alterations. Most known oncogenes were identified by gain-of-function mutations in cancer, yet little is known about their epigenetic features. Through integrative analysis of 11,596 epigenomic profiles and mutations from >8200 tumor-normal pair...
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/PMC7641226/ https://www.ncbi.nlm.nih.gov/pubmed/33144558 http://dx.doi.org/10.1038/s41467-020-18913-8 |
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author | Zhao, Dongyu Zhang, Lili Zhang, Min Xia, Bo Lv, Jie Gao, Xinlei Wang, Guangyu Meng, Qingshu Yi, Yang Zhu, Sen Tomoiaga, Alin S. Lee, Min Gyu Cooke, John P. Cao, Qi Chen, Kaifu |
author_facet | Zhao, Dongyu Zhang, Lili Zhang, Min Xia, Bo Lv, Jie Gao, Xinlei Wang, Guangyu Meng, Qingshu Yi, Yang Zhu, Sen Tomoiaga, Alin S. Lee, Min Gyu Cooke, John P. Cao, Qi Chen, Kaifu |
author_sort | Zhao, Dongyu |
collection | PubMed |
description | Cancers result from a set of genetic and epigenetic alterations. Most known oncogenes were identified by gain-of-function mutations in cancer, yet little is known about their epigenetic features. Through integrative analysis of 11,596 epigenomic profiles and mutations from >8200 tumor-normal pairs, we discover broad genic repression domains (BGRD) on chromatin as an epigenetic signature for oncogenes. A BGRD is a widespread enrichment domain of the repressive histone modification H3K27me3 and is further enriched with multiple other repressive marks including H3K9me3, H3K9me2, and H3K27me2. Further, BGRD displays widespread enrichment of repressed cis-regulatory elements. Shortening of BGRDs is linked to derepression of transcription. BGRDs at oncogenes tend to be conserved across normal cell types. Putative tumor-promoting genes and lncRNAs defined using BGRDs are experimentally verified as required for cancer phenotypes. Therefore, BGRDs play key roles in epigenetic regulation of cancer and provide a direction for mutation-independent discovery of oncogenes. |
format | Online Article Text |
id | pubmed-7641226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76412262020-11-10 Broad genic repression domains signify enhanced silencing of oncogenes Zhao, Dongyu Zhang, Lili Zhang, Min Xia, Bo Lv, Jie Gao, Xinlei Wang, Guangyu Meng, Qingshu Yi, Yang Zhu, Sen Tomoiaga, Alin S. Lee, Min Gyu Cooke, John P. Cao, Qi Chen, Kaifu Nat Commun Article Cancers result from a set of genetic and epigenetic alterations. Most known oncogenes were identified by gain-of-function mutations in cancer, yet little is known about their epigenetic features. Through integrative analysis of 11,596 epigenomic profiles and mutations from >8200 tumor-normal pairs, we discover broad genic repression domains (BGRD) on chromatin as an epigenetic signature for oncogenes. A BGRD is a widespread enrichment domain of the repressive histone modification H3K27me3 and is further enriched with multiple other repressive marks including H3K9me3, H3K9me2, and H3K27me2. Further, BGRD displays widespread enrichment of repressed cis-regulatory elements. Shortening of BGRDs is linked to derepression of transcription. BGRDs at oncogenes tend to be conserved across normal cell types. Putative tumor-promoting genes and lncRNAs defined using BGRDs are experimentally verified as required for cancer phenotypes. Therefore, BGRDs play key roles in epigenetic regulation of cancer and provide a direction for mutation-independent discovery of oncogenes. Nature Publishing Group UK 2020-11-03 /pmc/articles/PMC7641226/ /pubmed/33144558 http://dx.doi.org/10.1038/s41467-020-18913-8 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 Zhao, Dongyu Zhang, Lili Zhang, Min Xia, Bo Lv, Jie Gao, Xinlei Wang, Guangyu Meng, Qingshu Yi, Yang Zhu, Sen Tomoiaga, Alin S. Lee, Min Gyu Cooke, John P. Cao, Qi Chen, Kaifu Broad genic repression domains signify enhanced silencing of oncogenes |
title | Broad genic repression domains signify enhanced silencing of oncogenes |
title_full | Broad genic repression domains signify enhanced silencing of oncogenes |
title_fullStr | Broad genic repression domains signify enhanced silencing of oncogenes |
title_full_unstemmed | Broad genic repression domains signify enhanced silencing of oncogenes |
title_short | Broad genic repression domains signify enhanced silencing of oncogenes |
title_sort | broad genic repression domains signify enhanced silencing of oncogenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7641226/ https://www.ncbi.nlm.nih.gov/pubmed/33144558 http://dx.doi.org/10.1038/s41467-020-18913-8 |
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