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Mechanism of G1 arrest in the Drosophila eye imaginal disc

BACKGROUND: Most differentiating cells are arrested in G1-phase of the cell cycle and this proliferative quiescence appears important to allow differentiation programmes to be executed. An example occurs in the Drosophila eye imaginal disc, where all cells are synchronized and arrested in G1 phase p...

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Autores principales: Escudero, Luis M, Freeman, Matthew
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810524/
https://www.ncbi.nlm.nih.gov/pubmed/17335573
http://dx.doi.org/10.1186/1471-213X-7-13
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author Escudero, Luis M
Freeman, Matthew
author_facet Escudero, Luis M
Freeman, Matthew
author_sort Escudero, Luis M
collection PubMed
description BACKGROUND: Most differentiating cells are arrested in G1-phase of the cell cycle and this proliferative quiescence appears important to allow differentiation programmes to be executed. An example occurs in the Drosophila eye imaginal disc, where all cells are synchronized and arrested in G1 phase prior to making a fate choice either to initiate the first round of photoreceptor differentiation or to re-enter one terminal mitosis. RESULTS: We have analysed the mechanism of this temporally regulated G1-phase in order to develop an integrated model of this proliferative regulation. We find that an overlapping set of cell cycle inhibitors combine to form an efficient barrier to cell cycle progression. This barrier depends on both the primary secreted signals that drive retinal development, Dpp and Hh. Each of these has distinct, as well as partially overlapping functions, in ensuring that Cyclin E and dE2F1 are kept in check. Additionally, inhibition of Cyclin A by Roughex is essential, and this regulation is independent of Dpp and Hh. CONCLUSION: One implication of these results is to further support the idea that Cyclin A has important functions in S-phase entry as well as in mitosis. The unexpectedly complex network of regulation may reflect the importance of cells being uniformly ready to respond to the inductive signals that coordinate retinal differentiation.
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spelling pubmed-18105242007-03-07 Mechanism of G1 arrest in the Drosophila eye imaginal disc Escudero, Luis M Freeman, Matthew BMC Dev Biol Research Article BACKGROUND: Most differentiating cells are arrested in G1-phase of the cell cycle and this proliferative quiescence appears important to allow differentiation programmes to be executed. An example occurs in the Drosophila eye imaginal disc, where all cells are synchronized and arrested in G1 phase prior to making a fate choice either to initiate the first round of photoreceptor differentiation or to re-enter one terminal mitosis. RESULTS: We have analysed the mechanism of this temporally regulated G1-phase in order to develop an integrated model of this proliferative regulation. We find that an overlapping set of cell cycle inhibitors combine to form an efficient barrier to cell cycle progression. This barrier depends on both the primary secreted signals that drive retinal development, Dpp and Hh. Each of these has distinct, as well as partially overlapping functions, in ensuring that Cyclin E and dE2F1 are kept in check. Additionally, inhibition of Cyclin A by Roughex is essential, and this regulation is independent of Dpp and Hh. CONCLUSION: One implication of these results is to further support the idea that Cyclin A has important functions in S-phase entry as well as in mitosis. The unexpectedly complex network of regulation may reflect the importance of cells being uniformly ready to respond to the inductive signals that coordinate retinal differentiation. BioMed Central 2007-03-02 /pmc/articles/PMC1810524/ /pubmed/17335573 http://dx.doi.org/10.1186/1471-213X-7-13 Text en Copyright © 2007 Escudero and Freeman; 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
Escudero, Luis M
Freeman, Matthew
Mechanism of G1 arrest in the Drosophila eye imaginal disc
title Mechanism of G1 arrest in the Drosophila eye imaginal disc
title_full Mechanism of G1 arrest in the Drosophila eye imaginal disc
title_fullStr Mechanism of G1 arrest in the Drosophila eye imaginal disc
title_full_unstemmed Mechanism of G1 arrest in the Drosophila eye imaginal disc
title_short Mechanism of G1 arrest in the Drosophila eye imaginal disc
title_sort mechanism of g1 arrest in the drosophila eye imaginal disc
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810524/
https://www.ncbi.nlm.nih.gov/pubmed/17335573
http://dx.doi.org/10.1186/1471-213X-7-13
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