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Nucleoporin-mediated regulation of cell identity genes

The organization of the genome in the three-dimensional space of the nucleus is coupled with cell type-specific gene expression. However, how nuclear architecture influences transcription that governs cell identity remains unknown. Here, we show that nuclear pore complex (NPC) components Nup93 and N...

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Autores principales: Ibarra, Arkaitz, Benner, Chris, Tyagi, Swati, Cool, Jonah, Hetzer, Martin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110992/
https://www.ncbi.nlm.nih.gov/pubmed/27807035
http://dx.doi.org/10.1101/gad.287417.116
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author Ibarra, Arkaitz
Benner, Chris
Tyagi, Swati
Cool, Jonah
Hetzer, Martin W.
author_facet Ibarra, Arkaitz
Benner, Chris
Tyagi, Swati
Cool, Jonah
Hetzer, Martin W.
author_sort Ibarra, Arkaitz
collection PubMed
description The organization of the genome in the three-dimensional space of the nucleus is coupled with cell type-specific gene expression. However, how nuclear architecture influences transcription that governs cell identity remains unknown. Here, we show that nuclear pore complex (NPC) components Nup93 and Nup153 bind superenhancers (SE), regulatory structures that drive the expression of key genes that specify cell identity. We found that nucleoporin-associated SEs localize preferentially to the nuclear periphery, and absence of Nup153 and Nup93 results in dramatic transcriptional changes of SE-associated genes. Our results reveal a crucial role of NPC components in the regulation of cell type-specifying genes and highlight nuclear architecture as a regulatory layer of genome functions in cell fate.
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spelling pubmed-51109922017-04-15 Nucleoporin-mediated regulation of cell identity genes Ibarra, Arkaitz Benner, Chris Tyagi, Swati Cool, Jonah Hetzer, Martin W. Genes Dev Research Communication The organization of the genome in the three-dimensional space of the nucleus is coupled with cell type-specific gene expression. However, how nuclear architecture influences transcription that governs cell identity remains unknown. Here, we show that nuclear pore complex (NPC) components Nup93 and Nup153 bind superenhancers (SE), regulatory structures that drive the expression of key genes that specify cell identity. We found that nucleoporin-associated SEs localize preferentially to the nuclear periphery, and absence of Nup153 and Nup93 results in dramatic transcriptional changes of SE-associated genes. Our results reveal a crucial role of NPC components in the regulation of cell type-specifying genes and highlight nuclear architecture as a regulatory layer of genome functions in cell fate. Cold Spring Harbor Laboratory Press 2016-10-15 /pmc/articles/PMC5110992/ /pubmed/27807035 http://dx.doi.org/10.1101/gad.287417.116 Text en © 2016 Ibarra et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research Communication
Ibarra, Arkaitz
Benner, Chris
Tyagi, Swati
Cool, Jonah
Hetzer, Martin W.
Nucleoporin-mediated regulation of cell identity genes
title Nucleoporin-mediated regulation of cell identity genes
title_full Nucleoporin-mediated regulation of cell identity genes
title_fullStr Nucleoporin-mediated regulation of cell identity genes
title_full_unstemmed Nucleoporin-mediated regulation of cell identity genes
title_short Nucleoporin-mediated regulation of cell identity genes
title_sort nucleoporin-mediated regulation of cell identity genes
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5110992/
https://www.ncbi.nlm.nih.gov/pubmed/27807035
http://dx.doi.org/10.1101/gad.287417.116
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