Cargando…

The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling

The cell cycle is coordinated with differentiation during animal development. Here we report a cell-cycle-independent developmental role for a master cell-cycle regulator, the anaphase-promoting complex or cyclosome (APC/C), in the regulation of cell fate through modulation of Wingless (Wg) signalin...

Descripción completa

Detalles Bibliográficos
Autores principales: Martins, Torcato, Meghini, Francesco, Florio, Francesca, Kimata, Yuu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225405/
https://www.ncbi.nlm.nih.gov/pubmed/28041905
http://dx.doi.org/10.1016/j.devcel.2016.12.005
_version_ 1782493498732183552
author Martins, Torcato
Meghini, Francesco
Florio, Francesca
Kimata, Yuu
author_facet Martins, Torcato
Meghini, Francesco
Florio, Francesca
Kimata, Yuu
author_sort Martins, Torcato
collection PubMed
description The cell cycle is coordinated with differentiation during animal development. Here we report a cell-cycle-independent developmental role for a master cell-cycle regulator, the anaphase-promoting complex or cyclosome (APC/C), in the regulation of cell fate through modulation of Wingless (Wg) signaling. The APC/C controls both cell-cycle progression and postmitotic processes through ubiquitin-dependent proteolysis. Through an RNAi screen in the developing Drosophila eye, we found that partial APC/C inactivation severely inhibits retinal differentiation independently of cell-cycle defects. The differentiation inhibition coincides with hyperactivation of Wg signaling caused by the accumulation of a Wg modulator, Drosophila Nek2 (dNek2). The APC/C degrades dNek2 upon synchronous G1 arrest prior to differentiation, which allows retinal differentiation through local suppression of Wg signaling. We also provide evidence that decapentaplegic signaling may posttranslationally regulate this APC/C function. Thus, the APC/C coordinates cell-fate determination with the cell cycle through the modulation of developmental signaling pathways.
format Online
Article
Text
id pubmed-5225405
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-52254052017-01-19 The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling Martins, Torcato Meghini, Francesco Florio, Francesca Kimata, Yuu Dev Cell Article The cell cycle is coordinated with differentiation during animal development. Here we report a cell-cycle-independent developmental role for a master cell-cycle regulator, the anaphase-promoting complex or cyclosome (APC/C), in the regulation of cell fate through modulation of Wingless (Wg) signaling. The APC/C controls both cell-cycle progression and postmitotic processes through ubiquitin-dependent proteolysis. Through an RNAi screen in the developing Drosophila eye, we found that partial APC/C inactivation severely inhibits retinal differentiation independently of cell-cycle defects. The differentiation inhibition coincides with hyperactivation of Wg signaling caused by the accumulation of a Wg modulator, Drosophila Nek2 (dNek2). The APC/C degrades dNek2 upon synchronous G1 arrest prior to differentiation, which allows retinal differentiation through local suppression of Wg signaling. We also provide evidence that decapentaplegic signaling may posttranslationally regulate this APC/C function. Thus, the APC/C coordinates cell-fate determination with the cell cycle through the modulation of developmental signaling pathways. Cell Press 2017-01-09 /pmc/articles/PMC5225405/ /pubmed/28041905 http://dx.doi.org/10.1016/j.devcel.2016.12.005 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Martins, Torcato
Meghini, Francesco
Florio, Francesca
Kimata, Yuu
The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling
title The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling
title_full The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling
title_fullStr The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling
title_full_unstemmed The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling
title_short The APC/C Coordinates Retinal Differentiation with G1 Arrest through the Nek2-Dependent Modulation of Wingless Signaling
title_sort apc/c coordinates retinal differentiation with g1 arrest through the nek2-dependent modulation of wingless signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225405/
https://www.ncbi.nlm.nih.gov/pubmed/28041905
http://dx.doi.org/10.1016/j.devcel.2016.12.005
work_keys_str_mv AT martinstorcato theapcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT meghinifrancesco theapcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT floriofrancesca theapcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT kimatayuu theapcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT martinstorcato apcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT meghinifrancesco apcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT floriofrancesca apcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling
AT kimatayuu apcccoordinatesretinaldifferentiationwithg1arrestthroughthenek2dependentmodulationofwinglesssignaling