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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2005
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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. |
format | Text |
id | pubmed-1065252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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