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Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element

N-Oct-3 is a neuronal transcription factor widely expressed in the developing mammalian central nervous system, and necessary to maintain neural cell differentiation. The key role of N-Oct-3 in the transcriptional regulation of a multiplicity of genes is primarily due to the structural plasticity of...

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Autores principales: Alazard, Robert, Blaud, Magali, Elbaz, Shmouel, Vossen, Christine, Icre, Guillaume, Joseph, Gérard, Nieto, Laurence, Erard, Monique
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065252/
https://www.ncbi.nlm.nih.gov/pubmed/15767276
http://dx.doi.org/10.1093/nar/gki284
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author Alazard, Robert
Blaud, Magali
Elbaz, Shmouel
Vossen, Christine
Icre, Guillaume
Joseph, Gérard
Nieto, Laurence
Erard, Monique
author_facet Alazard, Robert
Blaud, Magali
Elbaz, Shmouel
Vossen, Christine
Icre, Guillaume
Joseph, Gérard
Nieto, Laurence
Erard, Monique
author_sort Alazard, Robert
collection PubMed
description N-Oct-3 is a neuronal transcription factor widely expressed in the developing mammalian central nervous system, and necessary to maintain neural cell differentiation. The key role of N-Oct-3 in the transcriptional regulation of a multiplicity of genes is primarily due to the structural plasticity of its so-called ‘POU’ (acronym of Pit, Oct, Unc) DNA-binding domain. We have recently reported about the unusual dual neuro-specific transcriptional regulation displayed by N-Oct-3 [Blaud,M., Vossen,C., Joseph,G., Alazard,R., Erard,M. and Nieto,L. (2004) J. Mol. Biol., 339, 1049–1058]. To elucidate the underlying molecular mechanisms, we have now made use of molecular modeling, DNA footprinting and electrophoretic mobility shift assay techniques. This combined approach has allowed us to uncover a novel mode of homodimerization adopted by the N-Oct-3 POU domain bound to the neuronal aromatic amino acids de-carboxylase and corticotropin-releasing hormone gene promoters and to demonstrate that this pattern is induced by a structural motif that we have termed ‘NORE’ (N-Oct-3 responsive element), comprising the 14 bp sequence element TNNRTAAATAATRN. In addition, we have been able to explain how the same structural motif can also induce the formation of a heterodimer in association with hepatocyte nuclear factor 3β(/Forkhead box a2). Finally, we discuss the possible role of the NORE motif in relation to neuroendocrine lung tumor formation, and in particular the development of small cell lung cancer.
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spelling pubmed-10652522005-03-15 Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element Alazard, Robert Blaud, Magali Elbaz, Shmouel Vossen, Christine Icre, Guillaume Joseph, Gérard Nieto, Laurence Erard, Monique Nucleic Acids Res Article N-Oct-3 is a neuronal transcription factor widely expressed in the developing mammalian central nervous system, and necessary to maintain neural cell differentiation. The key role of N-Oct-3 in the transcriptional regulation of a multiplicity of genes is primarily due to the structural plasticity of its so-called ‘POU’ (acronym of Pit, Oct, Unc) DNA-binding domain. We have recently reported about the unusual dual neuro-specific transcriptional regulation displayed by N-Oct-3 [Blaud,M., Vossen,C., Joseph,G., Alazard,R., Erard,M. and Nieto,L. (2004) J. Mol. Biol., 339, 1049–1058]. To elucidate the underlying molecular mechanisms, we have now made use of molecular modeling, DNA footprinting and electrophoretic mobility shift assay techniques. This combined approach has allowed us to uncover a novel mode of homodimerization adopted by the N-Oct-3 POU domain bound to the neuronal aromatic amino acids de-carboxylase and corticotropin-releasing hormone gene promoters and to demonstrate that this pattern is induced by a structural motif that we have termed ‘NORE’ (N-Oct-3 responsive element), comprising the 14 bp sequence element TNNRTAAATAATRN. In addition, we have been able to explain how the same structural motif can also induce the formation of a heterodimer in association with hepatocyte nuclear factor 3β(/Forkhead box a2). Finally, we discuss the possible role of the NORE motif in relation to neuroendocrine lung tumor formation, and in particular the development of small cell lung cancer. Oxford University Press 2005 2005-03-14 /pmc/articles/PMC1065252/ /pubmed/15767276 http://dx.doi.org/10.1093/nar/gki284 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Article
Alazard, Robert
Blaud, Magali
Elbaz, Shmouel
Vossen, Christine
Icre, Guillaume
Joseph, Gérard
Nieto, Laurence
Erard, Monique
Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element
title Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element
title_full Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element
title_fullStr Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element
title_full_unstemmed Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element
title_short Identification of the ‘NORE’ (N-Oct-3 responsive element), a novel structural motif and composite element
title_sort identification of the ‘nore’ (n-oct-3 responsive element), a novel structural motif and composite element
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1065252/
https://www.ncbi.nlm.nih.gov/pubmed/15767276
http://dx.doi.org/10.1093/nar/gki284
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