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A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors
BACKGROUND: Dynamic monitoring of protein expression and localization is fundamental to the understanding of biological processes. The paired-class homeodomain-containing transcription factor Otx2 is essential for normal head and brain development in vertebrates. Recent conditional knockout studies...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2204009/ https://www.ncbi.nlm.nih.gov/pubmed/17980036 http://dx.doi.org/10.1186/1471-213X-7-122 |
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author | Fossat, Nicolas Le Greneur, Coralie Béby, Francis Vincent, Stéphane Godement, Pierre Chatelain, Gilles Lamonerie, Thomas |
author_facet | Fossat, Nicolas Le Greneur, Coralie Béby, Francis Vincent, Stéphane Godement, Pierre Chatelain, Gilles Lamonerie, Thomas |
author_sort | Fossat, Nicolas |
collection | PubMed |
description | BACKGROUND: Dynamic monitoring of protein expression and localization is fundamental to the understanding of biological processes. The paired-class homeodomain-containing transcription factor Otx2 is essential for normal head and brain development in vertebrates. Recent conditional knockout studies have pointed to multiple roles of this protein during late development and post-natal life. Yet, later expression and functions remain poorly characterized as specific reagents to detect the protein at any stage of development are still missing. RESULTS: We generated a new mouse line harbouring an insertion of the GFP gene within the Otx2 coding sequence to monitor the gene activity while preserving most of its functions. Our results demonstrate that this line represents a convenient tool to capture the dynamics of Otx2 gene expression from early embryonic stages to adulthood. In addition, we could visualize the intracellular location of Otx2 protein. In the retina, we reinterpret the former view of protein distribution and show a further level of regulation of intranuclear protein localization, which depends on the cell type. CONCLUSION: The GFP-tagged Otx2 mouse line fully recapitulates previously known expression patterns and brings additional accuracy and easiness of detection of Otx2 gene activity. This opens up the way to live imaging of a highly dynamic actor of brain development and can be adapted to any mutant background to probe for genetic interaction between Otx2 and the mutated gene. |
format | Text |
id | pubmed-2204009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22040092008-01-17 A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors Fossat, Nicolas Le Greneur, Coralie Béby, Francis Vincent, Stéphane Godement, Pierre Chatelain, Gilles Lamonerie, Thomas BMC Dev Biol Methodology Article BACKGROUND: Dynamic monitoring of protein expression and localization is fundamental to the understanding of biological processes. The paired-class homeodomain-containing transcription factor Otx2 is essential for normal head and brain development in vertebrates. Recent conditional knockout studies have pointed to multiple roles of this protein during late development and post-natal life. Yet, later expression and functions remain poorly characterized as specific reagents to detect the protein at any stage of development are still missing. RESULTS: We generated a new mouse line harbouring an insertion of the GFP gene within the Otx2 coding sequence to monitor the gene activity while preserving most of its functions. Our results demonstrate that this line represents a convenient tool to capture the dynamics of Otx2 gene expression from early embryonic stages to adulthood. In addition, we could visualize the intracellular location of Otx2 protein. In the retina, we reinterpret the former view of protein distribution and show a further level of regulation of intranuclear protein localization, which depends on the cell type. CONCLUSION: The GFP-tagged Otx2 mouse line fully recapitulates previously known expression patterns and brings additional accuracy and easiness of detection of Otx2 gene activity. This opens up the way to live imaging of a highly dynamic actor of brain development and can be adapted to any mutant background to probe for genetic interaction between Otx2 and the mutated gene. BioMed Central 2007-11-02 /pmc/articles/PMC2204009/ /pubmed/17980036 http://dx.doi.org/10.1186/1471-213X-7-122 Text en Copyright © 2007 Fossat et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Fossat, Nicolas Le Greneur, Coralie Béby, Francis Vincent, Stéphane Godement, Pierre Chatelain, Gilles Lamonerie, Thomas A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors |
title | A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors |
title_full | A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors |
title_fullStr | A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors |
title_full_unstemmed | A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors |
title_short | A new GFP-tagged line reveals unexpected Otx2 protein localization in retinal photoreceptors |
title_sort | new gfp-tagged line reveals unexpected otx2 protein localization in retinal photoreceptors |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2204009/ https://www.ncbi.nlm.nih.gov/pubmed/17980036 http://dx.doi.org/10.1186/1471-213X-7-122 |
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