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Eye Selector Logic for a Coordinated Cell Cycle Exit

Organ-selector transcription factors control simultaneously cell differentiation and proliferation, ensuring the development of functional organs and their homeostasis. How this is achieved at the molecular level is still unclear. Here we have investigated how the transcriptional pulse of string/cdc...

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Detalles Bibliográficos
Autores principales: Lopes, Carla S., Casares, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335009/
https://www.ncbi.nlm.nih.gov/pubmed/25695251
http://dx.doi.org/10.1371/journal.pgen.1004981
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author Lopes, Carla S.
Casares, Fernando
author_facet Lopes, Carla S.
Casares, Fernando
author_sort Lopes, Carla S.
collection PubMed
description Organ-selector transcription factors control simultaneously cell differentiation and proliferation, ensuring the development of functional organs and their homeostasis. How this is achieved at the molecular level is still unclear. Here we have investigated how the transcriptional pulse of string/cdc25 (stg), the universal mitotic trigger, is regulated during Drosophila retina development as an example of coordinated deployment of differentiation and proliferation programs. We identify the eye specific stg enhancer, stg-FMW, and show that Pax6 selector genes, in cooperation with Eya and So, two members of the retinal determination network, activate stg-FMW, establishing a positive feed-forward loop. This loop is negatively modulated by the Meis1 protein, Hth. This regulatory logic is reminiscent of that controlling the expression of differentiation transcription factors. Our work shows that subjecting transcription factors and key cell cycle regulators to the same regulatory logic ensures the coupling between differentiation and proliferation programs during organ development.
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spelling pubmed-43350092015-02-24 Eye Selector Logic for a Coordinated Cell Cycle Exit Lopes, Carla S. Casares, Fernando PLoS Genet Research Article Organ-selector transcription factors control simultaneously cell differentiation and proliferation, ensuring the development of functional organs and their homeostasis. How this is achieved at the molecular level is still unclear. Here we have investigated how the transcriptional pulse of string/cdc25 (stg), the universal mitotic trigger, is regulated during Drosophila retina development as an example of coordinated deployment of differentiation and proliferation programs. We identify the eye specific stg enhancer, stg-FMW, and show that Pax6 selector genes, in cooperation with Eya and So, two members of the retinal determination network, activate stg-FMW, establishing a positive feed-forward loop. This loop is negatively modulated by the Meis1 protein, Hth. This regulatory logic is reminiscent of that controlling the expression of differentiation transcription factors. Our work shows that subjecting transcription factors and key cell cycle regulators to the same regulatory logic ensures the coupling between differentiation and proliferation programs during organ development. Public Library of Science 2015-02-19 /pmc/articles/PMC4335009/ /pubmed/25695251 http://dx.doi.org/10.1371/journal.pgen.1004981 Text en © 2015 Lopes, Casares http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lopes, Carla S.
Casares, Fernando
Eye Selector Logic for a Coordinated Cell Cycle Exit
title Eye Selector Logic for a Coordinated Cell Cycle Exit
title_full Eye Selector Logic for a Coordinated Cell Cycle Exit
title_fullStr Eye Selector Logic for a Coordinated Cell Cycle Exit
title_full_unstemmed Eye Selector Logic for a Coordinated Cell Cycle Exit
title_short Eye Selector Logic for a Coordinated Cell Cycle Exit
title_sort eye selector logic for a coordinated cell cycle exit
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335009/
https://www.ncbi.nlm.nih.gov/pubmed/25695251
http://dx.doi.org/10.1371/journal.pgen.1004981
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