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Exploration of nucleosome positioning patterns in transcription factor function

The binding of transcription factors (TFs) triggers activation of specific chromatin regions through the recruitment and activation of RNA polymerase. Unique nucleosome positioning (NP) occurs during gene expression and has been suggested to be involved in various other chromatin functions. However,...

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Autores principales: Maehara, Kazumitsu, Ohkawa, Yasuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726364/
https://www.ncbi.nlm.nih.gov/pubmed/26790608
http://dx.doi.org/10.1038/srep19620
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author Maehara, Kazumitsu
Ohkawa, Yasuyuki
author_facet Maehara, Kazumitsu
Ohkawa, Yasuyuki
author_sort Maehara, Kazumitsu
collection PubMed
description The binding of transcription factors (TFs) triggers activation of specific chromatin regions through the recruitment and activation of RNA polymerase. Unique nucleosome positioning (NP) occurs during gene expression and has been suggested to be involved in various other chromatin functions. However, the diversity of NP that can occur for each function has not been clarified. Here we used MNase-Seq data to evaluate NP around 258 cis-regulatory elements in the mouse genome. Principal component analysis of the 258 elements revealed that NP consisted of five major patterns. Furthermore, the five NP patterns had predictive power for the level of gene expression. We also demonstrated that selective NP patterns appeared around TF binding sites. These results suggest that the NP patterns are correlated to specific functions on chromatin.
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spelling pubmed-47263642016-01-27 Exploration of nucleosome positioning patterns in transcription factor function Maehara, Kazumitsu Ohkawa, Yasuyuki Sci Rep Article The binding of transcription factors (TFs) triggers activation of specific chromatin regions through the recruitment and activation of RNA polymerase. Unique nucleosome positioning (NP) occurs during gene expression and has been suggested to be involved in various other chromatin functions. However, the diversity of NP that can occur for each function has not been clarified. Here we used MNase-Seq data to evaluate NP around 258 cis-regulatory elements in the mouse genome. Principal component analysis of the 258 elements revealed that NP consisted of five major patterns. Furthermore, the five NP patterns had predictive power for the level of gene expression. We also demonstrated that selective NP patterns appeared around TF binding sites. These results suggest that the NP patterns are correlated to specific functions on chromatin. Nature Publishing Group 2016-01-21 /pmc/articles/PMC4726364/ /pubmed/26790608 http://dx.doi.org/10.1038/srep19620 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Maehara, Kazumitsu
Ohkawa, Yasuyuki
Exploration of nucleosome positioning patterns in transcription factor function
title Exploration of nucleosome positioning patterns in transcription factor function
title_full Exploration of nucleosome positioning patterns in transcription factor function
title_fullStr Exploration of nucleosome positioning patterns in transcription factor function
title_full_unstemmed Exploration of nucleosome positioning patterns in transcription factor function
title_short Exploration of nucleosome positioning patterns in transcription factor function
title_sort exploration of nucleosome positioning patterns in transcription factor function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726364/
https://www.ncbi.nlm.nih.gov/pubmed/26790608
http://dx.doi.org/10.1038/srep19620
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