Your browser doesn't support javascript.
loading
Cell size homeostasis is maintained by CDK4-dependent activation of p38 MAPK.
Tan, Ceryl; Ginzberg, Miriam B; Webster, Rachel; Iyengar, Seshu; Liu, Shixuan; Papadopoli, David; Concannon, John; Wang, Yuan; Auld, Douglas S; Jenkins, Jeremy L; Rost, Hannes; Topisirovic, Ivan; Hilfinger, Andreas; Derry, W Brent; Patel, Nish; Kafri, Ran.
Affiliation
  • Tan C; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1A8, Canada; Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Ginzberg MB; Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Webster R; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1A8, Canada; Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Iyengar S; Department of Chemical and Physical Sciences, University of Toronto Mississauga, ON L5L 1C6, Canada.
  • Liu S; Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
  • Papadopoli D; Gerald Bronfman Department of Oncology and Lady Davis Institute, McGill University Montreal, QC H4A 3T2, Canada.
  • Concannon J; Novartis Institutes for BioMedical Research, Cambridge, MA 02139, USA.
  • Wang Y; Novartis Institutes for BioMedical Research, Cambridge, MA 02139, USA.
  • Auld DS; Novartis Institutes for BioMedical Research, Cambridge, MA 02139, USA.
  • Jenkins JL; Novartis Institutes for BioMedical Research, Cambridge, MA 02139, USA.
  • Rost H; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1A8, Canada.
  • Topisirovic I; Gerald Bronfman Department of Oncology and Lady Davis Institute, McGill University Montreal, QC H4A 3T2, Canada.
  • Hilfinger A; Department of Chemical and Physical Sciences, University of Toronto Mississauga, ON L5L 1C6, Canada.
  • Derry WB; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1A8, Canada; Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Patel N; Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Kafri R; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1A8, Canada; Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada. Electronic address: ran.kafri@sickkids.ca.
Dev Cell ; 56(12): 1756-1769.e7, 2021 06 21.
Article in En | MEDLINE | ID: mdl-34022133
ABSTRACT
While molecules that promote the growth of animal cells have been identified, it remains unclear how such signals are orchestrated to determine a characteristic target size for different cell types. It is increasingly clear that cell size is determined by size checkpoints-mechanisms that restrict the cell cycle progression of cells that are smaller than their target size. Previously, we described a p38 MAPK-dependent cell size checkpoint mechanism whereby p38 is selectively activated and prevents cell cycle progression in cells that are smaller than a given target size. In this study, we show that the specific target size required for inactivation of p38 and transition through the cell cycle is determined by CDK4 activity. Our data suggest a model whereby p38 and CDK4 cooperate analogously to the function of a thermostat while p38 senses irregularities in size, CDK4 corresponds to the thermostat dial that sets the target size.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Cycle / P38 Mitogen-Activated Protein Kinases / Cell Size / Cyclin-Dependent Kinase 4 Type of study: Prognostic_studies Limits: Humans Language: En Journal: Dev Cell Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Cycle / P38 Mitogen-Activated Protein Kinases / Cell Size / Cyclin-Dependent Kinase 4 Type of study: Prognostic_studies Limits: Humans Language: En Journal: Dev Cell Year: 2021 Document type: Article