A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle

Cell cycle control: Order in time achieved by dynamic coupling A dynamic coupling of cyclin-dependent kinase with transcription factors in yeast offers insights into the timely cell cycle progression. An international team lead by Matteo Barberis from University of Amsterdam in The Netherlands studi...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Christian Linke, Anastasia Chasapi, Alberto González-Novo, Istabrak Al Sawad, Silvia Tognetti, Edda Klipp, Mart Loog, Sylvia Krobitsch, Francesc Posas, Ioannis Xenarios, Matteo Barberis
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
Acceso en línea:https://doaj.org/article/b97661edfbb74ad691b7c34f9005b5f8
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:b97661edfbb74ad691b7c34f9005b5f8
record_format dspace
spelling oai:doaj.org-article:b97661edfbb74ad691b7c34f9005b5f82021-12-02T16:08:59ZA Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle10.1038/s41540-017-0008-12056-7189https://doaj.org/article/b97661edfbb74ad691b7c34f9005b5f82017-03-01T00:00:00Zhttps://doi.org/10.1038/s41540-017-0008-1https://doaj.org/toc/2056-7189Cell cycle control: Order in time achieved by dynamic coupling A dynamic coupling of cyclin-dependent kinase with transcription factors in yeast offers insights into the timely cell cycle progression. An international team lead by Matteo Barberis from University of Amsterdam in The Netherlands studied the molecular mechanisms responsible for the coordination of DNA replication with cell division. The researchers have demonstrated how the sequential order of waves of mitotic cyclins activating cyclin-dependent kinase, or Cdk, is achieved by synchronizing Cdk with transcriptional activities. They have generated a mathematical model that predicts a cyclin/Cdk-mediated regulation of an activator molecule to stimulate mitotic cyclin expression. This prediction was successfully validated experimentally, identifying Forkhead transcription factors, or Fkh, as pivotal molecules. Cyclin waves are temporally synchronized by Fkh, and a mitotic Clb/Cdk1-mediated regulation of Fkh modulates cyclin expression. The findings reveal a novel principle of design, with kinase and transcription activities interlocked to guarantee a timely cell cycle.Christian LinkeAnastasia ChasapiAlberto González-NovoIstabrak Al SawadSilvia TognettiEdda KlippMart LoogSylvia KrobitschFrancesc PosasIoannis XenariosMatteo BarberisNature PortfolioarticleBiology (General)QH301-705.5ENnpj Systems Biology and Applications, Vol 3, Iss 1, Pp 1-12 (2017)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Christian Linke
Anastasia Chasapi
Alberto González-Novo
Istabrak Al Sawad
Silvia Tognetti
Edda Klipp
Mart Loog
Sylvia Krobitsch
Francesc Posas
Ioannis Xenarios
Matteo Barberis
A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle
description Cell cycle control: Order in time achieved by dynamic coupling A dynamic coupling of cyclin-dependent kinase with transcription factors in yeast offers insights into the timely cell cycle progression. An international team lead by Matteo Barberis from University of Amsterdam in The Netherlands studied the molecular mechanisms responsible for the coordination of DNA replication with cell division. The researchers have demonstrated how the sequential order of waves of mitotic cyclins activating cyclin-dependent kinase, or Cdk, is achieved by synchronizing Cdk with transcriptional activities. They have generated a mathematical model that predicts a cyclin/Cdk-mediated regulation of an activator molecule to stimulate mitotic cyclin expression. This prediction was successfully validated experimentally, identifying Forkhead transcription factors, or Fkh, as pivotal molecules. Cyclin waves are temporally synchronized by Fkh, and a mitotic Clb/Cdk1-mediated regulation of Fkh modulates cyclin expression. The findings reveal a novel principle of design, with kinase and transcription activities interlocked to guarantee a timely cell cycle.
format article
author Christian Linke
Anastasia Chasapi
Alberto González-Novo
Istabrak Al Sawad
Silvia Tognetti
Edda Klipp
Mart Loog
Sylvia Krobitsch
Francesc Posas
Ioannis Xenarios
Matteo Barberis
author_facet Christian Linke
Anastasia Chasapi
Alberto González-Novo
Istabrak Al Sawad
Silvia Tognetti
Edda Klipp
Mart Loog
Sylvia Krobitsch
Francesc Posas
Ioannis Xenarios
Matteo Barberis
author_sort Christian Linke
title A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle
title_short A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle
title_full A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle
title_fullStr A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle
title_full_unstemmed A Clb/Cdk1-mediated regulation of Fkh2 synchronizes CLB expression in the budding yeast cell cycle
title_sort clb/cdk1-mediated regulation of fkh2 synchronizes clb expression in the budding yeast cell cycle
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/b97661edfbb74ad691b7c34f9005b5f8
work_keys_str_mv AT christianlinke aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT anastasiachasapi aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT albertogonzaleznovo aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT istabrakalsawad aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT silviatognetti aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT eddaklipp aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT martloog aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT sylviakrobitsch aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT francescposas aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT ioannisxenarios aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT matteobarberis aclbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT christianlinke clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT anastasiachasapi clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT albertogonzaleznovo clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT istabrakalsawad clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT silviatognetti clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT eddaklipp clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT martloog clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT sylviakrobitsch clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT francescposas clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT ioannisxenarios clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
AT matteobarberis clbcdk1mediatedregulationoffkh2synchronizesclbexpressioninthebuddingyeastcellcycle
_version_ 1718384491683119104