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A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina

BACKGROUND: Otx genes, orthologues of the Drosophila orthodenticle gene (otd), play crucial roles in vertebrate brain development. In the Xenopus eye, Xotx2 and Xotx5b promote bipolar and photoreceptor cell fates, respectively. The molecular basis of their differential action is not completely under...

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Autores principales: Onorati, Marco, Cremisi, Federico, Liu, Yang, He, Rong-Qiao, Barsacchi, Giuseppina, Vignali, Robert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1929070/
https://www.ncbi.nlm.nih.gov/pubmed/17597530
http://dx.doi.org/10.1186/1749-8104-2-12
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author Onorati, Marco
Cremisi, Federico
Liu, Yang
He, Rong-Qiao
Barsacchi, Giuseppina
Vignali, Robert
author_facet Onorati, Marco
Cremisi, Federico
Liu, Yang
He, Rong-Qiao
Barsacchi, Giuseppina
Vignali, Robert
author_sort Onorati, Marco
collection PubMed
description BACKGROUND: Otx genes, orthologues of the Drosophila orthodenticle gene (otd), play crucial roles in vertebrate brain development. In the Xenopus eye, Xotx2 and Xotx5b promote bipolar and photoreceptor cell fates, respectively. The molecular basis of their differential action is not completely understood, though the carboxyl termini of the two proteins seem to be crucial. To define the molecular domains that make the action of these proteins so different, and to determine whether their retinal abilities are shared by Drosophila OTD, we performed an in vivo molecular dissection of their activity by transfecting retinal progenitors with several wild-type, deletion and chimeric constructs of Xotx2, Xotx5b and otd. RESULTS: We identified a small 8–10 amino acid divergent region, directly downstream of the homeodomain, that is crucial for the respective activities of XOTX2 and XOTX5b. In lipofection experiments, the exchange of this 'specificity box' completely switches the retinal activity of XOTX5b into that of XOTX2 and vice versa. Moreover, the insertion of this box into Drosophila OTD, which has no effect on retinal cell fate, endows it with the specific activity of either XOTX protein. Significantly, in cell transfection experiments, the diverse ability of XOTX2 and XOTX5b to synergize with NRL, a cofactor essential for vertebrate rod development, to transactivate the rhodopsin promoter is also switched depending on the box. We also show by GST-pull down that XOTX2 and XOTX5b differentially interact with NRL, though this property is not strictly dependent on the box. CONCLUSION: Our data provide molecular evidence on how closely related homeodomain gene products can differentiate their functions to regulate distinct cell fates. A small 'specificity box' is both necessary and sufficient to confer on XOTX2 and XOTX5b their distinct activities in the developing frog retina and to convert the neutral orthologous OTD protein of Drosophila into a positive and specific XOTX-like retinal regulator. Relatively little is known of what gives developmental specificity to homeodomain regulators. We propose that this box is a major domain of XOTX proteins that provides them with the appropriate developmental specificity in retinal histogenesis.
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spelling pubmed-19290702007-07-21 A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina Onorati, Marco Cremisi, Federico Liu, Yang He, Rong-Qiao Barsacchi, Giuseppina Vignali, Robert Neural Develop Research Article BACKGROUND: Otx genes, orthologues of the Drosophila orthodenticle gene (otd), play crucial roles in vertebrate brain development. In the Xenopus eye, Xotx2 and Xotx5b promote bipolar and photoreceptor cell fates, respectively. The molecular basis of their differential action is not completely understood, though the carboxyl termini of the two proteins seem to be crucial. To define the molecular domains that make the action of these proteins so different, and to determine whether their retinal abilities are shared by Drosophila OTD, we performed an in vivo molecular dissection of their activity by transfecting retinal progenitors with several wild-type, deletion and chimeric constructs of Xotx2, Xotx5b and otd. RESULTS: We identified a small 8–10 amino acid divergent region, directly downstream of the homeodomain, that is crucial for the respective activities of XOTX2 and XOTX5b. In lipofection experiments, the exchange of this 'specificity box' completely switches the retinal activity of XOTX5b into that of XOTX2 and vice versa. Moreover, the insertion of this box into Drosophila OTD, which has no effect on retinal cell fate, endows it with the specific activity of either XOTX protein. Significantly, in cell transfection experiments, the diverse ability of XOTX2 and XOTX5b to synergize with NRL, a cofactor essential for vertebrate rod development, to transactivate the rhodopsin promoter is also switched depending on the box. We also show by GST-pull down that XOTX2 and XOTX5b differentially interact with NRL, though this property is not strictly dependent on the box. CONCLUSION: Our data provide molecular evidence on how closely related homeodomain gene products can differentiate their functions to regulate distinct cell fates. A small 'specificity box' is both necessary and sufficient to confer on XOTX2 and XOTX5b their distinct activities in the developing frog retina and to convert the neutral orthologous OTD protein of Drosophila into a positive and specific XOTX-like retinal regulator. Relatively little is known of what gives developmental specificity to homeodomain regulators. We propose that this box is a major domain of XOTX proteins that provides them with the appropriate developmental specificity in retinal histogenesis. BioMed Central 2007-06-27 /pmc/articles/PMC1929070/ /pubmed/17597530 http://dx.doi.org/10.1186/1749-8104-2-12 Text en Copyright © 2007 Onorati 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 Research Article
Onorati, Marco
Cremisi, Federico
Liu, Yang
He, Rong-Qiao
Barsacchi, Giuseppina
Vignali, Robert
A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina
title A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina
title_full A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina
title_fullStr A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina
title_full_unstemmed A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina
title_short A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina
title_sort specific box switches the cell fate determining activity of xotx2 and xotx5b in the xenopus retina
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1929070/
https://www.ncbi.nlm.nih.gov/pubmed/17597530
http://dx.doi.org/10.1186/1749-8104-2-12
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