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Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism

Fibroblast growth factor 1 (FGF1) is involved in muscle development and regeneration. The FGF1 gene contains four tissue-specific promoters allowing synthesis of four transcripts with distinct leader regions. Two of these transcripts contain internal ribosome entry sites (IRESs), which are RNA eleme...

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Autores principales: Conte, Caroline, Ainaoui, Nadera, Delluc-Clavières, Aurélie, Khoury, Marie P., Azar, Rania, Pujol, Françoise, Martineau, Yvan, Pyronnet, Stéphane, Prats, Anne-Catherine
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760804/
https://www.ncbi.nlm.nih.gov/pubmed/19561198
http://dx.doi.org/10.1093/nar/gkp550
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author Conte, Caroline
Ainaoui, Nadera
Delluc-Clavières, Aurélie
Khoury, Marie P.
Azar, Rania
Pujol, Françoise
Martineau, Yvan
Pyronnet, Stéphane
Prats, Anne-Catherine
author_facet Conte, Caroline
Ainaoui, Nadera
Delluc-Clavières, Aurélie
Khoury, Marie P.
Azar, Rania
Pujol, Françoise
Martineau, Yvan
Pyronnet, Stéphane
Prats, Anne-Catherine
author_sort Conte, Caroline
collection PubMed
description Fibroblast growth factor 1 (FGF1) is involved in muscle development and regeneration. The FGF1 gene contains four tissue-specific promoters allowing synthesis of four transcripts with distinct leader regions. Two of these transcripts contain internal ribosome entry sites (IRESs), which are RNA elements allowing mRNA translation to occur in conditions of blockade of the classical cap-dependent mechanism. Here, we investigated the function and the regulation of FGF1 during muscle differentiation and regeneration. Our data show that FGF1 protein expression is induced in differentiating myoblasts and regenerating mouse muscle, whereas siRNA knock-down demonstrated FGF1 requirement for myoblast differentiation. FGF1 induction occurred at both transcriptional and translational levels, involving specific activation of both promoter A and IRES A, whereas global cap-dependent translation was inhibited. Furthermore, we identified, in the FGF1 promoter A distal region, a cis-acting element able to activate the IRES A-driven translation. These data revealed a mechanism of molecular coupling of mRNA transcription and translation, involving a unique process of IRES activation by a promoter element. The crucial role of FGF1 in myoblast differentiation provides physiological relevance to this novel mechanism. This finding also provides a new insight into the molecular mechanisms linking different levels of gene expression regulation.
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spelling pubmed-27608042009-10-13 Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism Conte, Caroline Ainaoui, Nadera Delluc-Clavières, Aurélie Khoury, Marie P. Azar, Rania Pujol, Françoise Martineau, Yvan Pyronnet, Stéphane Prats, Anne-Catherine Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Fibroblast growth factor 1 (FGF1) is involved in muscle development and regeneration. The FGF1 gene contains four tissue-specific promoters allowing synthesis of four transcripts with distinct leader regions. Two of these transcripts contain internal ribosome entry sites (IRESs), which are RNA elements allowing mRNA translation to occur in conditions of blockade of the classical cap-dependent mechanism. Here, we investigated the function and the regulation of FGF1 during muscle differentiation and regeneration. Our data show that FGF1 protein expression is induced in differentiating myoblasts and regenerating mouse muscle, whereas siRNA knock-down demonstrated FGF1 requirement for myoblast differentiation. FGF1 induction occurred at both transcriptional and translational levels, involving specific activation of both promoter A and IRES A, whereas global cap-dependent translation was inhibited. Furthermore, we identified, in the FGF1 promoter A distal region, a cis-acting element able to activate the IRES A-driven translation. These data revealed a mechanism of molecular coupling of mRNA transcription and translation, involving a unique process of IRES activation by a promoter element. The crucial role of FGF1 in myoblast differentiation provides physiological relevance to this novel mechanism. This finding also provides a new insight into the molecular mechanisms linking different levels of gene expression regulation. Oxford University Press 2009-09 2009-06-26 /pmc/articles/PMC2760804/ /pubmed/19561198 http://dx.doi.org/10.1093/nar/gkp550 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene Regulation, Chromatin and Epigenetics
Conte, Caroline
Ainaoui, Nadera
Delluc-Clavières, Aurélie
Khoury, Marie P.
Azar, Rania
Pujol, Françoise
Martineau, Yvan
Pyronnet, Stéphane
Prats, Anne-Catherine
Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
title Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
title_full Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
title_fullStr Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
title_full_unstemmed Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
title_short Fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
title_sort fibroblast growth factor 1 induced during myogenesis by a transcription–translation coupling mechanism
topic Gene Regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2760804/
https://www.ncbi.nlm.nih.gov/pubmed/19561198
http://dx.doi.org/10.1093/nar/gkp550
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