Your browser doesn't support javascript.
loading
Eukaryotic cell biology is temporally coordinated to support the energetic demands of protein homeostasis.
O'Neill, John S; Hoyle, Nathaniel P; Robertson, J Brian; Edgar, Rachel S; Beale, Andrew D; Peak-Chew, Sew Y; Day, Jason; Costa, Ana S H; Frezza, Christian; Causton, Helen C.
Afiliação
  • O'Neill JS; MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK. oneillj@mrc-lmb.cam.ac.uk.
  • Hoyle NP; MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.
  • Robertson JB; Middle Tennessee State University, Murfreesboro, TN, 37132, USA.
  • Edgar RS; Molecular Virology, Department of Medicine, Imperial College, London, W2 1NY, UK.
  • Beale AD; MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.
  • Peak-Chew SY; MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.
  • Day J; Department of Earth Sciences, University of Cambridge, Cambridge, CB2 3EQ, UK.
  • Costa ASH; MRC Cancer Unit, University of Cambridge, Cambridge, CB2 0XZ, UK.
  • Frezza C; Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
  • Causton HC; MRC Cancer Unit, University of Cambridge, Cambridge, CB2 0XZ, UK.
Nat Commun ; 11(1): 4706, 2020 09 17.
Article em En | MEDLINE | ID: mdl-32943618
ABSTRACT
Yeast physiology is temporally regulated, this becomes apparent under nutrient-limited conditions and results in respiratory oscillations (YROs). YROs share features with circadian rhythms and interact with, but are independent of, the cell division cycle. Here, we show that YROs minimise energy expenditure by restricting protein synthesis until sufficient resources are stored, while maintaining osmotic homeostasis and protein quality control. Although nutrient supply is constant, cells sequester and store metabolic resources via increased transport, autophagy and biomolecular condensation. Replete stores trigger increased H+ export which stimulates TORC1 and liberates proteasomes, ribosomes, chaperones and metabolic enzymes from non-membrane bound compartments. This facilitates translational bursting, liquidation of storage carbohydrates, increased ATP turnover, and the export of osmolytes. We propose that dynamic regulation of ion transport and metabolic plasticity are required to maintain osmotic and protein homeostasis during remodelling of eukaryotic proteomes, and that bioenergetic constraints selected for temporal organisation that promotes oscillatory behaviour.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Metabolismo Energético / Células Eucarióticas / Proteostase Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Metabolismo Energético / Células Eucarióticas / Proteostase Idioma: En Ano de publicação: 2020 Tipo de documento: Article