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Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation

TAF4 (TATA-binding protein-associated factor 4) and its paralogue TAF4b are components of the TFIID core module. We inactivated the murine Taf4a gene to address Taf4 function during embryogenesis. Here we show that Taf4a(−/−) embryos survive until E9.5 where primary germ layers and many embryonic st...

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Autores principales: Langer, Diana, Martianov, Igor, Alpern, Daniel, Rhinn, Muriel, Keime, Céline, Dollé, Pascal, Mengus, Gabrielle, Davidson, Irwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820908/
https://www.ncbi.nlm.nih.gov/pubmed/27026076
http://dx.doi.org/10.1038/ncomms11063
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author Langer, Diana
Martianov, Igor
Alpern, Daniel
Rhinn, Muriel
Keime, Céline
Dollé, Pascal
Mengus, Gabrielle
Davidson, Irwin
author_facet Langer, Diana
Martianov, Igor
Alpern, Daniel
Rhinn, Muriel
Keime, Céline
Dollé, Pascal
Mengus, Gabrielle
Davidson, Irwin
author_sort Langer, Diana
collection PubMed
description TAF4 (TATA-binding protein-associated factor 4) and its paralogue TAF4b are components of the TFIID core module. We inactivated the murine Taf4a gene to address Taf4 function during embryogenesis. Here we show that Taf4a(−/−) embryos survive until E9.5 where primary germ layers and many embryonic structures are identified showing Taf4 is dispensable for their specification. In contrast, Taf4 is required for correct patterning of the trunk and anterior structures, ventral morphogenesis and proper heart positioning. Overlapping expression of Taf4a and Taf4b during embryogenesis suggests their redundancy at early stages. In agreement with this, Taf4a(−/−) embryonic stem cells (ESCs) are viable and comprise Taf4b-containing TFIID. Nevertheless, Taf4a(−/−) ESCs do not complete differentiation into glutamatergic neurons and cardiomyocytes in vitro due to impaired preinitiation complex formation at the promoters of critical differentiation genes. We define an essential role of a core TFIID TAF in differentiation events during mammalian embryogenesis.
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spelling pubmed-48209082016-04-17 Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation Langer, Diana Martianov, Igor Alpern, Daniel Rhinn, Muriel Keime, Céline Dollé, Pascal Mengus, Gabrielle Davidson, Irwin Nat Commun Article TAF4 (TATA-binding protein-associated factor 4) and its paralogue TAF4b are components of the TFIID core module. We inactivated the murine Taf4a gene to address Taf4 function during embryogenesis. Here we show that Taf4a(−/−) embryos survive until E9.5 where primary germ layers and many embryonic structures are identified showing Taf4 is dispensable for their specification. In contrast, Taf4 is required for correct patterning of the trunk and anterior structures, ventral morphogenesis and proper heart positioning. Overlapping expression of Taf4a and Taf4b during embryogenesis suggests their redundancy at early stages. In agreement with this, Taf4a(−/−) embryonic stem cells (ESCs) are viable and comprise Taf4b-containing TFIID. Nevertheless, Taf4a(−/−) ESCs do not complete differentiation into glutamatergic neurons and cardiomyocytes in vitro due to impaired preinitiation complex formation at the promoters of critical differentiation genes. We define an essential role of a core TFIID TAF in differentiation events during mammalian embryogenesis. Nature Publishing Group 2016-03-30 /pmc/articles/PMC4820908/ /pubmed/27026076 http://dx.doi.org/10.1038/ncomms11063 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Langer, Diana
Martianov, Igor
Alpern, Daniel
Rhinn, Muriel
Keime, Céline
Dollé, Pascal
Mengus, Gabrielle
Davidson, Irwin
Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation
title Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation
title_full Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation
title_fullStr Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation
title_full_unstemmed Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation
title_short Essential role of the TFIID subunit TAF4 in murine embryogenesis and embryonic stem cell differentiation
title_sort essential role of the tfiid subunit taf4 in murine embryogenesis and embryonic stem cell differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820908/
https://www.ncbi.nlm.nih.gov/pubmed/27026076
http://dx.doi.org/10.1038/ncomms11063
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