TOR signalling regulates mitotic commitment through stress-activated MAPK and Polo kinase in response to nutrient stress

Janni Petersen

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Cell growth and cell division are coupled to control cell size and this co-ordination is often modulated by the availability of nutrients. In many eukaryotes, TOR (target of rapamycin) signalling is involved in coupling nutrient sensing to cell growth and division controls. Nutrient stress inhibits TOR signalling to advance the timing of cell division and thus leads to continued cell division at reduced cell size. Most changes in the environment stimulate stress-activated MAPK (mitogen-activated protein kinase) signalling pathways. Several MAPKs also have a general role in the control of mitotic onset and cell division. In the present paper, I discuss the interplay between two major signalling pathways, the TOR and the stress MAPK signalling pathways, in controlling mitotic commitment, with the main focus being on fission yeast (Schizosaccharomyces pombe). © The Authors Journal compilation © 2009 Biochemical Society.
    Original languageEnglish
    Pages (from-to)273-277
    Number of pages4
    JournalBiochemical Society Transactions
    Volume37
    Issue number1
    DOIs
    Publication statusPublished - 2009

    Keywords

    • Mitogen-activated protein kinase (MAPK)
    • Mitotic commitment
    • Nutrient stress
    • Polo kinase
    • Target of rapamycin (TOR)
    • Yeast

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