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Differential contribution to gene expression prediction of histone modifications at enhancers or promoters
The ChIP-seq signal of histone modifications at promoters is a good predictor of gene expression in different cellular contexts, but whether this is also true at enhancers is not clear. To address this issue, we develop quantitative models to characterize the relationship of gene expression with his...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443064/ https://www.ncbi.nlm.nih.gov/pubmed/34473698 http://dx.doi.org/10.1371/journal.pcbi.1009368 |
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author | González-Ramírez, Mar Ballaré, Cecilia Mugianesi, Francesca Beringer, Malte Santanach, Alexandra Blanco, Enrique Di Croce, Luciano |
author_facet | González-Ramírez, Mar Ballaré, Cecilia Mugianesi, Francesca Beringer, Malte Santanach, Alexandra Blanco, Enrique Di Croce, Luciano |
author_sort | González-Ramírez, Mar |
collection | PubMed |
description | The ChIP-seq signal of histone modifications at promoters is a good predictor of gene expression in different cellular contexts, but whether this is also true at enhancers is not clear. To address this issue, we develop quantitative models to characterize the relationship of gene expression with histone modifications at enhancers or promoters. We use embryonic stem cells (ESCs), which contain a full spectrum of active and repressed (poised) enhancers, to train predictive models. As many poised enhancers in ESCs switch towards an active state during differentiation, predictive models can also be trained on poised enhancers throughout differentiation and in development. Remarkably, we determine that histone modifications at enhancers, as well as promoters, are predictive of gene expression in ESCs and throughout differentiation and development. Importantly, we demonstrate that their contribution to the predictive models varies depending on their location in enhancers or promoters. Moreover, we use a local regression (LOESS) to normalize sequencing data from different sources, which allows us to apply predictive models trained in a specific cellular context to a different one. We conclude that the relationship between gene expression and histone modifications at enhancers is universal and different from promoters. Our study provides new insight into how histone modifications relate to gene expression based on their location in enhancers or promoters. |
format | Online Article Text |
id | pubmed-8443064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84430642021-09-16 Differential contribution to gene expression prediction of histone modifications at enhancers or promoters González-Ramírez, Mar Ballaré, Cecilia Mugianesi, Francesca Beringer, Malte Santanach, Alexandra Blanco, Enrique Di Croce, Luciano PLoS Comput Biol Research Article The ChIP-seq signal of histone modifications at promoters is a good predictor of gene expression in different cellular contexts, but whether this is also true at enhancers is not clear. To address this issue, we develop quantitative models to characterize the relationship of gene expression with histone modifications at enhancers or promoters. We use embryonic stem cells (ESCs), which contain a full spectrum of active and repressed (poised) enhancers, to train predictive models. As many poised enhancers in ESCs switch towards an active state during differentiation, predictive models can also be trained on poised enhancers throughout differentiation and in development. Remarkably, we determine that histone modifications at enhancers, as well as promoters, are predictive of gene expression in ESCs and throughout differentiation and development. Importantly, we demonstrate that their contribution to the predictive models varies depending on their location in enhancers or promoters. Moreover, we use a local regression (LOESS) to normalize sequencing data from different sources, which allows us to apply predictive models trained in a specific cellular context to a different one. We conclude that the relationship between gene expression and histone modifications at enhancers is universal and different from promoters. Our study provides new insight into how histone modifications relate to gene expression based on their location in enhancers or promoters. Public Library of Science 2021-09-02 /pmc/articles/PMC8443064/ /pubmed/34473698 http://dx.doi.org/10.1371/journal.pcbi.1009368 Text en © 2021 González-Ramírez et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article González-Ramírez, Mar Ballaré, Cecilia Mugianesi, Francesca Beringer, Malte Santanach, Alexandra Blanco, Enrique Di Croce, Luciano Differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
title | Differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
title_full | Differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
title_fullStr | Differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
title_full_unstemmed | Differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
title_short | Differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
title_sort | differential contribution to gene expression prediction of histone modifications at enhancers or promoters |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443064/ https://www.ncbi.nlm.nih.gov/pubmed/34473698 http://dx.doi.org/10.1371/journal.pcbi.1009368 |
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