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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
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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. |
format | Text |
id | pubmed-2891705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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