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Prediction of histone post-translational modification patterns based on nascent transcription data
The role of histone modifications in transcription remains incompletely understood. Here we examine the relationship between histone modifications and transcription using experimental perturbations combined with sensitive machine-learning tools. Transcription predicted the variation in active histon...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444190/ https://www.ncbi.nlm.nih.gov/pubmed/35273399 http://dx.doi.org/10.1038/s41588-022-01026-x |
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author | Wang, Zhong Chivu, Alexandra G. Choate, Lauren A. Rice, Edward J. Miller, Donald C. Chu, Tinyi Chou, Shao-Pei Kingsley, Nicole B. Petersen, Jessica L. Finno, Carrie J. Bellone, Rebecca R. Antczak, Douglas F. Lis, John T. Danko, Charles G. |
author_facet | Wang, Zhong Chivu, Alexandra G. Choate, Lauren A. Rice, Edward J. Miller, Donald C. Chu, Tinyi Chou, Shao-Pei Kingsley, Nicole B. Petersen, Jessica L. Finno, Carrie J. Bellone, Rebecca R. Antczak, Douglas F. Lis, John T. Danko, Charles G. |
author_sort | Wang, Zhong |
collection | PubMed |
description | The role of histone modifications in transcription remains incompletely understood. Here we examine the relationship between histone modifications and transcription using experimental perturbations combined with sensitive machine-learning tools. Transcription predicted the variation in active histone marks and complex chromatin states, like bivalent promoters, down to single-nucleosome resolution and at an accuracy that rivaled the correspondence between independent ChIP-seq experiments. Blocking transcription rapidly removed two punctate marks, H3K4me3 and H3K27ac, from chromatin indicating that transcription is required for active histone modifications. Transcription was also required for maintenance of H3K27me3 consistent with a role for RNA in recruiting PRC2. A subset of DNase-I hypersensitive sites were refractory to prediction, precluding models where transcription initiates pervasively at any open chromatin. Our results, in combination with past literature, support a model in which active histone modifications serve a supportive, rather than an essential regulatory, role in transcription. |
format | Online Article Text |
id | pubmed-9444190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-94441902022-09-10 Prediction of histone post-translational modification patterns based on nascent transcription data Wang, Zhong Chivu, Alexandra G. Choate, Lauren A. Rice, Edward J. Miller, Donald C. Chu, Tinyi Chou, Shao-Pei Kingsley, Nicole B. Petersen, Jessica L. Finno, Carrie J. Bellone, Rebecca R. Antczak, Douglas F. Lis, John T. Danko, Charles G. Nat Genet Article The role of histone modifications in transcription remains incompletely understood. Here we examine the relationship between histone modifications and transcription using experimental perturbations combined with sensitive machine-learning tools. Transcription predicted the variation in active histone marks and complex chromatin states, like bivalent promoters, down to single-nucleosome resolution and at an accuracy that rivaled the correspondence between independent ChIP-seq experiments. Blocking transcription rapidly removed two punctate marks, H3K4me3 and H3K27ac, from chromatin indicating that transcription is required for active histone modifications. Transcription was also required for maintenance of H3K27me3 consistent with a role for RNA in recruiting PRC2. A subset of DNase-I hypersensitive sites were refractory to prediction, precluding models where transcription initiates pervasively at any open chromatin. Our results, in combination with past literature, support a model in which active histone modifications serve a supportive, rather than an essential regulatory, role in transcription. 2022-03 2022-03-10 /pmc/articles/PMC9444190/ /pubmed/35273399 http://dx.doi.org/10.1038/s41588-022-01026-x Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Wang, Zhong Chivu, Alexandra G. Choate, Lauren A. Rice, Edward J. Miller, Donald C. Chu, Tinyi Chou, Shao-Pei Kingsley, Nicole B. Petersen, Jessica L. Finno, Carrie J. Bellone, Rebecca R. Antczak, Douglas F. Lis, John T. Danko, Charles G. Prediction of histone post-translational modification patterns based on nascent transcription data |
title | Prediction of histone post-translational modification patterns based on nascent transcription data |
title_full | Prediction of histone post-translational modification patterns based on nascent transcription data |
title_fullStr | Prediction of histone post-translational modification patterns based on nascent transcription data |
title_full_unstemmed | Prediction of histone post-translational modification patterns based on nascent transcription data |
title_short | Prediction of histone post-translational modification patterns based on nascent transcription data |
title_sort | prediction of histone post-translational modification patterns based on nascent transcription data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444190/ https://www.ncbi.nlm.nih.gov/pubmed/35273399 http://dx.doi.org/10.1038/s41588-022-01026-x |
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