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Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality
Formation of nucleosome free region (NFR) accompanied by specific histone modifications at flanking nucleosomes is an important prerequisite for enhancer and promoter activity. Due to this process, active regulatory elements often exhibit a distinct shape of histone signal in the form of a peak-vall...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872112/ https://www.ncbi.nlm.nih.gov/pubmed/27095194 http://dx.doi.org/10.1093/nar/gkw250 |
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author | Pundhir, Sachin Bagger, Frederik O. Lauridsen, Felicia B. Rapin, Nicolas Porse, Bo T. |
author_facet | Pundhir, Sachin Bagger, Frederik O. Lauridsen, Felicia B. Rapin, Nicolas Porse, Bo T. |
author_sort | Pundhir, Sachin |
collection | PubMed |
description | Formation of nucleosome free region (NFR) accompanied by specific histone modifications at flanking nucleosomes is an important prerequisite for enhancer and promoter activity. Due to this process, active regulatory elements often exhibit a distinct shape of histone signal in the form of a peak-valley-peak (PVP) pattern. However, different features of PVP patterns and their robustness in predicting active regulatory elements have never been systematically analyzed. Here, we present PARE, a novel computational method that systematically analyzes the H3K4me1 or H3K4me3 PVP patterns to predict NFRs. We show that NFRs predicted by H3K4me1 and me3 patterns are associated with active enhancers and promoters, respectively. Furthermore, asymmetry in the height of peaks flanking the central valley can predict the directionality of stable transcription at promoters. Using PARE on ChIP-seq histone modifications from four ENCODE cell lines and four hematopoietic differentiation stages, we identified several enhancers whose regulatory activity is stage specific and correlates positively with the expression of proximal genes in a particular stage. In conclusion, our results demonstrate that PVP patterns delineate both the histone modification landscape and the transcriptional activities governed by active enhancers and promoters, and therefore can be used for their prediction. PARE is freely available at http://servers.binf.ku.dk/pare. |
format | Online Article Text |
id | pubmed-4872112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48721122016-05-27 Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality Pundhir, Sachin Bagger, Frederik O. Lauridsen, Felicia B. Rapin, Nicolas Porse, Bo T. Nucleic Acids Res Computational Biology Formation of nucleosome free region (NFR) accompanied by specific histone modifications at flanking nucleosomes is an important prerequisite for enhancer and promoter activity. Due to this process, active regulatory elements often exhibit a distinct shape of histone signal in the form of a peak-valley-peak (PVP) pattern. However, different features of PVP patterns and their robustness in predicting active regulatory elements have never been systematically analyzed. Here, we present PARE, a novel computational method that systematically analyzes the H3K4me1 or H3K4me3 PVP patterns to predict NFRs. We show that NFRs predicted by H3K4me1 and me3 patterns are associated with active enhancers and promoters, respectively. Furthermore, asymmetry in the height of peaks flanking the central valley can predict the directionality of stable transcription at promoters. Using PARE on ChIP-seq histone modifications from four ENCODE cell lines and four hematopoietic differentiation stages, we identified several enhancers whose regulatory activity is stage specific and correlates positively with the expression of proximal genes in a particular stage. In conclusion, our results demonstrate that PVP patterns delineate both the histone modification landscape and the transcriptional activities governed by active enhancers and promoters, and therefore can be used for their prediction. PARE is freely available at http://servers.binf.ku.dk/pare. Oxford University Press 2016-05-19 2016-04-19 /pmc/articles/PMC4872112/ /pubmed/27095194 http://dx.doi.org/10.1093/nar/gkw250 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Computational Biology Pundhir, Sachin Bagger, Frederik O. Lauridsen, Felicia B. Rapin, Nicolas Porse, Bo T. Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
title | Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
title_full | Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
title_fullStr | Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
title_full_unstemmed | Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
title_short | Peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
title_sort | peak-valley-peak pattern of histone modifications delineates active regulatory elements and their directionality |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872112/ https://www.ncbi.nlm.nih.gov/pubmed/27095194 http://dx.doi.org/10.1093/nar/gkw250 |
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