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CDK1, the Other 'Master Regulator' of Autophagy.
Odle, Richard I; Florey, Oliver; Ktistakis, Nicholas T; Cook, Simon J.
Afiliação
  • Odle RI; Signalling Laboratory, The Babraham Institute, Babraham Research Campus, Cambridge, CB22 3AT, UK.
  • Florey O; Signalling Laboratory, The Babraham Institute, Babraham Research Campus, Cambridge, CB22 3AT, UK.
  • Ktistakis NT; Signalling Laboratory, The Babraham Institute, Babraham Research Campus, Cambridge, CB22 3AT, UK.
  • Cook SJ; Signalling Laboratory, The Babraham Institute, Babraham Research Campus, Cambridge, CB22 3AT, UK. Electronic address: simon.cook@babraham.ac.uk.
Trends Cell Biol ; 31(2): 95-107, 2021 02.
Article em En | MEDLINE | ID: mdl-33272830
ABSTRACT
Autophagy and cap-dependent mRNA translation are tightly regulated by the mechanistic target of rapamycin complex 1 (mTORC1) signalling complex in response to nutrient availability. However, the regulation of these processes, and mTORC1 itself, is different during mitosis, and this has remained an area of significant controversy; for example, studies have argued that autophagy is either repressed or highly active during mitosis. Recent studies have shown that autophagy initiation is repressed, and cap-dependent mRNA translation is maintained during mitosis despite mTORC1 activity being repressed. This is achieved in large part by a switch from mTORC1- to cyclin-dependent kinase 1 (CDK1)-mediated regulation. Here, we review the history and recent advances and seek to present a unifying model to inform the future study of autophagy and mTORC1 during mitosis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Autofagia / Proteína Quinase CDC2 / Alvo Mecanístico do Complexo 1 de Rapamicina / Mitose Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Trends Cell Biol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Autofagia / Proteína Quinase CDC2 / Alvo Mecanístico do Complexo 1 de Rapamicina / Mitose Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Trends Cell Biol Ano de publicação: 2021 Tipo de documento: Article