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Cells Escape an Operational Mitotic Checkpoint through a Stochastic Process.
Bonaiuti, Paolo; Chiroli, Elena; Gross, Fridolin; Corno, Andrea; Vernieri, Claudio; Stefl, Martin; Cosentino Lagomarsino, Marco; Knop, Michael; Ciliberto, Andrea.
Afiliação
  • Bonaiuti P; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy.
  • Chiroli E; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy.
  • Gross F; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy.
  • Corno A; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy.
  • Vernieri C; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy; Medical Oncology Department, Fondazione IRCCS Istituto Nazionale Tumori, via Venezian 1, 20133 Milan, Italy.
  • Stefl M; DKFZ-ZMBH Alliance, Centre for Molecular Biology (ZMBH), University of Heidelberg, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.
  • Cosentino Lagomarsino M; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy; Sorbonne Universités, UPMC Univ Paris 06, 5 Place Jussieu, 75005 Paris, France; CNRS, UMR 7238 "Biologie Computationnelle et Quantitative," UPMC, Institut de Biologie Paris Seine, 4 Place Jussieu, 75005 Paris, France.
  • Knop M; DKFZ-ZMBH Alliance, Centre for Molecular Biology (ZMBH), University of Heidelberg, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany; DKFZ-ZMBH Alliance, Department of Cell and Tumour Biology, German Cancer Research Centre (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
  • Ciliberto A; Istituto Firc di Oncologia Molecolare, IFOM, via Adamello 16, 20139 Milan, Italy; Istituto di Genetica Molecolare, Consiglio Nazionale delle Ricerche (IGM-CNR), via Abbiategrasso 207, 27100 Pavia, Italy. Electronic address: andrea.ciliberto@ifom.eu.
Curr Biol ; 28(1): 28-37.e7, 2018 01 08.
Article em En | MEDLINE | ID: mdl-29249657
Improperly attached chromosomes activate the mitotic checkpoint that arrests cell division before anaphase. Cells can maintain an arrest for several hours but eventually will resume proliferation, a process we refer to as adaptation. Whether adapting cells bypass an active block or whether the block has to be removed to resume proliferation is not clear. Likewise, it is not known whether all cells of a genetically homogeneous population are equally capable to adapt. Here, we show that the mitotic checkpoint is operational when yeast cells adapt and that each cell has the same propensity to adapt. Our results are consistent with a model of the mitotic checkpoint where adaptation is driven by random fluctuations of APC/CCdc20, the molecular species inhibited by the checkpoint. Our data provide a quantitative framework for understanding how cells overcome a constant stimulus that halts cell cycle progression.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Cromossomos Fúngicos / Nocodazol / Moduladores de Tubulina / Pontos de Checagem da Fase M do Ciclo Celular Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Cromossomos Fúngicos / Nocodazol / Moduladores de Tubulina / Pontos de Checagem da Fase M do Ciclo Celular Idioma: En Ano de publicação: 2018 Tipo de documento: Article