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Endoreplication Controls Cell Fate Maintenance

Cell-fate specification is typically thought to precede and determine cell-cycle regulation during differentiation. Here we show that endoreplication, also known as endoreduplication, a specialized cell-cycle variant often associated with cell differentiation but also frequently occurring in maligna...

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Autores principales: Bramsiepe, Jonathan, Wester, Katja, Weinl, Christina, Roodbarkelari, Farshad, Kasili, Remmy, Larkin, John C., Hülskamp, Martin, Schnittger, Arp
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891705/
https://www.ncbi.nlm.nih.gov/pubmed/20585618
http://dx.doi.org/10.1371/journal.pgen.1000996
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author Bramsiepe, Jonathan
Wester, Katja
Weinl, Christina
Roodbarkelari, Farshad
Kasili, Remmy
Larkin, John C.
Hülskamp, Martin
Schnittger, Arp
author_facet Bramsiepe, Jonathan
Wester, Katja
Weinl, Christina
Roodbarkelari, Farshad
Kasili, Remmy
Larkin, John C.
Hülskamp, Martin
Schnittger, Arp
author_sort Bramsiepe, Jonathan
collection PubMed
description Cell-fate specification is typically thought to precede and determine cell-cycle regulation during differentiation. Here we show that endoreplication, also known as endoreduplication, a specialized cell-cycle variant often associated with cell differentiation but also frequently occurring in malignant cells, plays a role in maintaining cell fate. For our study we have used Arabidopsis trichomes as a model system and have manipulated endoreplication levels via mutants of cell-cycle regulators and overexpression of cell-cycle inhibitors under a trichome-specific promoter. Strikingly, a reduction of endoreplication resulted in reduced trichome numbers and caused trichomes to lose their identity. Live observations of young Arabidopsis leaves revealed that dedifferentiating trichomes re-entered mitosis and were re-integrated into the epidermal pavement-cell layer, acquiring the typical characteristics of the surrounding epidermal cells. Conversely, when we promoted endoreplication in glabrous patterning mutants, trichome fate could be restored, demonstrating that endoreplication is an important determinant of cell identity. Our data lead to a new model of cell-fate control and tissue integrity during development by revealing a cell-fate quality control system at the tissue level.
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spelling pubmed-28917052010-06-28 Endoreplication Controls Cell Fate Maintenance Bramsiepe, Jonathan Wester, Katja Weinl, Christina Roodbarkelari, Farshad Kasili, Remmy Larkin, John C. Hülskamp, Martin Schnittger, Arp PLoS Genet Research Article Cell-fate specification is typically thought to precede and determine cell-cycle regulation during differentiation. Here we show that endoreplication, also known as endoreduplication, a specialized cell-cycle variant often associated with cell differentiation but also frequently occurring in malignant cells, plays a role in maintaining cell fate. For our study we have used Arabidopsis trichomes as a model system and have manipulated endoreplication levels via mutants of cell-cycle regulators and overexpression of cell-cycle inhibitors under a trichome-specific promoter. Strikingly, a reduction of endoreplication resulted in reduced trichome numbers and caused trichomes to lose their identity. Live observations of young Arabidopsis leaves revealed that dedifferentiating trichomes re-entered mitosis and were re-integrated into the epidermal pavement-cell layer, acquiring the typical characteristics of the surrounding epidermal cells. Conversely, when we promoted endoreplication in glabrous patterning mutants, trichome fate could be restored, demonstrating that endoreplication is an important determinant of cell identity. Our data lead to a new model of cell-fate control and tissue integrity during development by revealing a cell-fate quality control system at the tissue level. Public Library of Science 2010-06-24 /pmc/articles/PMC2891705/ /pubmed/20585618 http://dx.doi.org/10.1371/journal.pgen.1000996 Text en Bramsiepe et al. 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
Bramsiepe, Jonathan
Wester, Katja
Weinl, Christina
Roodbarkelari, Farshad
Kasili, Remmy
Larkin, John C.
Hülskamp, Martin
Schnittger, Arp
Endoreplication Controls Cell Fate Maintenance
title Endoreplication Controls Cell Fate Maintenance
title_full Endoreplication Controls Cell Fate Maintenance
title_fullStr Endoreplication Controls Cell Fate Maintenance
title_full_unstemmed Endoreplication Controls Cell Fate Maintenance
title_short Endoreplication Controls Cell Fate Maintenance
title_sort endoreplication controls cell fate maintenance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891705/
https://www.ncbi.nlm.nih.gov/pubmed/20585618
http://dx.doi.org/10.1371/journal.pgen.1000996
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