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Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation
BACKGROUND: Recent studies have underscored the role of enhancers in defining cell type-specific transcriptomes. Cell type-specific enhancers are bound by combinations of shared and cell type-specific transcription factors (TFs). However, little is known about combinatorial binding of TFs to enhance...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304210/ https://www.ncbi.nlm.nih.gov/pubmed/25560382 http://dx.doi.org/10.1186/1471-2164-15-S10-S4 |
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author | Vandenbon, Alexis Teraguchi, Shunsuke Takeuchi, Osamu Suzuki, Yutaka Standley, Daron M |
author_facet | Vandenbon, Alexis Teraguchi, Shunsuke Takeuchi, Osamu Suzuki, Yutaka Standley, Daron M |
author_sort | Vandenbon, Alexis |
collection | PubMed |
description | BACKGROUND: Recent studies have underscored the role of enhancers in defining cell type-specific transcriptomes. Cell type-specific enhancers are bound by combinations of shared and cell type-specific transcription factors (TFs). However, little is known about combinatorial binding of TFs to enhancers, dynamics of TF binding following stimulation, or the downstream effects on gene expression. Here, we address these questions in two types of myeloid antigen presenting cells (APCs), macrophages and dendritic cells (DCs), before and after stimulation with lipopolysaccharide (LPS), a potent stimulator of the innate immune response. RESULTS: We classified enhancers according to the combination of TFs binding them. There were significant correlations between the sets of TFs bound to enhancers prior to stimulation and expression changes of nearby genes after stimulation. Importantly, a set of enhancers pre-bound by PU.1, C/EBPβ, ATF3, IRF4, and JunB was strongly associated with induced genes and binding by stimulus-activated regulators. Our classification suggests that transient loss of ATF3 binding to a subset of these enhancers is important for regulation of early-induced genes. Changes in TF-enhancer binding after stimulation were correlated with binding by additional activated TFs and with the presence of proximally located enhancers. CONCLUSIONS: The results presented in this study reveal the complexity and dynamics of TF- enhancer binding before and after stimulation in myeloid APCs. |
format | Online Article Text |
id | pubmed-4304210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43042102015-02-09 Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation Vandenbon, Alexis Teraguchi, Shunsuke Takeuchi, Osamu Suzuki, Yutaka Standley, Daron M BMC Genomics Research BACKGROUND: Recent studies have underscored the role of enhancers in defining cell type-specific transcriptomes. Cell type-specific enhancers are bound by combinations of shared and cell type-specific transcription factors (TFs). However, little is known about combinatorial binding of TFs to enhancers, dynamics of TF binding following stimulation, or the downstream effects on gene expression. Here, we address these questions in two types of myeloid antigen presenting cells (APCs), macrophages and dendritic cells (DCs), before and after stimulation with lipopolysaccharide (LPS), a potent stimulator of the innate immune response. RESULTS: We classified enhancers according to the combination of TFs binding them. There were significant correlations between the sets of TFs bound to enhancers prior to stimulation and expression changes of nearby genes after stimulation. Importantly, a set of enhancers pre-bound by PU.1, C/EBPβ, ATF3, IRF4, and JunB was strongly associated with induced genes and binding by stimulus-activated regulators. Our classification suggests that transient loss of ATF3 binding to a subset of these enhancers is important for regulation of early-induced genes. Changes in TF-enhancer binding after stimulation were correlated with binding by additional activated TFs and with the presence of proximally located enhancers. CONCLUSIONS: The results presented in this study reveal the complexity and dynamics of TF- enhancer binding before and after stimulation in myeloid APCs. BioMed Central 2014-12-12 /pmc/articles/PMC4304210/ /pubmed/25560382 http://dx.doi.org/10.1186/1471-2164-15-S10-S4 Text en Copyright © 2014 Vandenbon et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Vandenbon, Alexis Teraguchi, Shunsuke Takeuchi, Osamu Suzuki, Yutaka Standley, Daron M Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation |
title | Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation |
title_full | Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation |
title_fullStr | Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation |
title_full_unstemmed | Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation |
title_short | Dynamics of enhancers in myeloid antigen presenting cells upon LPS stimulation |
title_sort | dynamics of enhancers in myeloid antigen presenting cells upon lps stimulation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304210/ https://www.ncbi.nlm.nih.gov/pubmed/25560382 http://dx.doi.org/10.1186/1471-2164-15-S10-S4 |
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