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Reference - PMID:23333317 - Removal of centrosomal PP1 by NIMA kinase unlocks the MPF feedback loop to promote mitotic commitment in S. pombe.

Reference summary

PubMed ID
PMID:23333317
Title
Removal of centrosomal PP1 by NIMA kinase unlocks the MPF feedback loop to promote mitotic commitment in S. pombe.
Authors
Grallert A, Chan KY, Alonso-Nuñez ML, Madrid M, Biswas A, Alvarez-Tabarés I, Connolly Y, Tanaka K, Robertson A, Ortiz JM, Smith DL, Hagan IM
Citation
Curr Biol 2013 Feb 04;23(3):213-22
Publication year
2013
Abstract
Activation of the Cdk1/cyclin B complex, also known as mitosis-promoting factor (MPF), drives commitment to mitosis. Interphase MPF is inhibited through phosphorylation of Cdk1 by Wee1-related kinases. Because Cdc25 phosphatases remove this phosphate, Cdc25 activity is an essential part of the switch that drives cells into mitosis. The generation of a critical "trigger" of active MPF promotes a positive feedback loop that employs Polo kinase to boost Cdc25 activity and inhibit Wee1, thereby ensuring that mitotic commitment is a bistable switch. Mutations in the spindle pole body (SPB) component Cut12 suppress otherwise lethal deficiencies in Cdc25. Cut12 harbors a bipartite protein phosphatase 1 (PP1) docking domain. Mutation of either element alone suppressed the temperature-dependent lethality of cdc25.22, whereas simultaneous ablation of both allowed cells to divide in the complete absence of Cdc25. Late G2 phase phosphorylation between the two elements by MPF and the NIMA kinase Fin1 blocked PP1(Dis2) recruitment, thereby promoting recruitment of Polo to Cut12 and the SPB and elevating global Polo kinase activity throughout the cell. PP1 recruitment to Cut12 sets a threshold for Polo's feedback-loop activity that locks the cell in interphase until Cdc25 pushes MPF activity through this barrier to initiate mitosis. We propose that events on the SPB (and, by inference, the centrosome) integrate inputs from diverse signaling networks to generate a coherent decision to divide that is appropriate for the particular environmental context of each cell. PP1 recruitment sets one or more critical thresholds for single or multiple local events within this switch.

Annotation

GO biological process

GO:0010972 - negative regulation of G2/M transition of mitotic cell cycle

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GO:0010971 - positive regulation of G2/M transition of mitotic cell cycle

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GO:0010389 - regulation of G2/M transition of mitotic cell cycle

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GO molecular function

GO:0004693 - cyclin-dependent protein serine/threonine kinase activity

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GO:0005515 - protein binding

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GO:0004674 - protein serine/threonine kinase activity

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GO:0035591 - signaling adaptor activity

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Modification

MOD:00047 - O-phospho-L-threonine

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Multi-locus phenotype

FYPO:0004481 - abolished cell population growth at high temperature

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FYPO:0000082 - decreased cell population growth at high temperature

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FYPO:0000674 - normal cell population growth at high temperature

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FYPO:0007474 - variable cell size at division

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FYPO:0001492 - viable elongated vegetative cell

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FYPO:0006822 - viable small vegetative cell with normal cell growth rate

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Single locus phenotype

FYPO:0002033 - abolished protein phosphorylation during vegetative growth

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FYPO:0000705 - abolished protein-protein interaction

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FYPO:0003331 - decreased protein kinase activity during mitotic interphase

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FYPO:0000940 - decreased protein localization to mitotic spindle pole body

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FYPO:0002821 - decreased protein localization to mitotic spindle pole body during interphase

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FYPO:0001838 - decreased protein phosphorylation during vegetative growth

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FYPO:0001645 - decreased protein-protein interaction

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FYPO:0007475 - delayed onset of protein localization to mitotic spindle pole body

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FYPO:0007385 - increased duration of protein-protein interaction

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FYPO:0007183 - increased protein kinase activity during mitotic interphase

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FYPO:0001571 - increased protein-protein interaction

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FYPO:0002967 - normal protein localization to mitotic spindle pole body

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FYPO:0000703 - normal protein-protein interaction

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FYPO:0006824 - premature protein localization to mitotic spindle pole body

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