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Shared transcription factors contribute to distinct cell fates

Genome-wide transcription factor (TF) binding profiles differ dramatically between cell types. However, not much is known about the relationship between cell-type-specific binding patterns and gene expression. A recent study demonstrated how the same TFs can have functional roles when binding to lar...

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Detalles Bibliográficos
Autores principales: Ng, Felicia SL, Calero-Nieto, Fernando J, Göttgens, Berthold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581352/
https://www.ncbi.nlm.nih.gov/pubmed/25425188
http://dx.doi.org/10.4161/21541264.2014.978173
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author Ng, Felicia SL
Calero-Nieto, Fernando J
Göttgens, Berthold
author_facet Ng, Felicia SL
Calero-Nieto, Fernando J
Göttgens, Berthold
author_sort Ng, Felicia SL
collection PubMed
description Genome-wide transcription factor (TF) binding profiles differ dramatically between cell types. However, not much is known about the relationship between cell-type-specific binding patterns and gene expression. A recent study demonstrated how the same TFs can have functional roles when binding to largely non-overlapping genomic regions in hematopoietic progenitor and mast cells. Cell-type specific binding profiles of shared TFs are therefore not merely the consequence of opportunistic and functionally irrelevant binding to accessible chromatin, but instead have the potential to make meaningful contributions to cell-type specific transcriptional programs.
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spelling pubmed-45813522016-01-06 Shared transcription factors contribute to distinct cell fates Ng, Felicia SL Calero-Nieto, Fernando J Göttgens, Berthold Transcription Point of View Genome-wide transcription factor (TF) binding profiles differ dramatically between cell types. However, not much is known about the relationship between cell-type-specific binding patterns and gene expression. A recent study demonstrated how the same TFs can have functional roles when binding to largely non-overlapping genomic regions in hematopoietic progenitor and mast cells. Cell-type specific binding profiles of shared TFs are therefore not merely the consequence of opportunistic and functionally irrelevant binding to accessible chromatin, but instead have the potential to make meaningful contributions to cell-type specific transcriptional programs. Taylor & Francis 2015-01-06 /pmc/articles/PMC4581352/ /pubmed/25425188 http://dx.doi.org/10.4161/21541264.2014.978173 Text en © 2014 The Author(s). © 2014 Taylor & Francis Group, LLC http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Point of View
Ng, Felicia SL
Calero-Nieto, Fernando J
Göttgens, Berthold
Shared transcription factors contribute to distinct cell fates
title Shared transcription factors contribute to distinct cell fates
title_full Shared transcription factors contribute to distinct cell fates
title_fullStr Shared transcription factors contribute to distinct cell fates
title_full_unstemmed Shared transcription factors contribute to distinct cell fates
title_short Shared transcription factors contribute to distinct cell fates
title_sort shared transcription factors contribute to distinct cell fates
topic Point of View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581352/
https://www.ncbi.nlm.nih.gov/pubmed/25425188
http://dx.doi.org/10.4161/21541264.2014.978173
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