Polo-like kinase-2 is required for centriole duplication in mammalian cells (Q24298744)

regulation of centriole replication

GOA release 2020-03-11

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GOA release 2020-03-11

5

Urs Hoffmann-Rohrer

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author name string

Silke Warnke

1

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Stefan Kemmler

2

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Rebecca S Hames

3

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Hsiao-Lun Tsai

4

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Andrew M Fry

6

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Ingrid Hoffmann

Cyclin-dependent kinase 2 (Cdk2) is required for centrosome duplication in mammalian cells

7

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language of work or name

English

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publication date

13 July 2004

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published in

Current Biology

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volume

14

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issue

13

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page(s)

1200-7

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cites work

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Centrosome duplication in mammalian somatic cells requires E2F and Cdk2-cyclin A.

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Polar expeditions--provisioning the centrosome for mitosis.

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Centrosome aberrations: cause or consequence of cancer progression?

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Activation of Cdc2/cyclin B and inhibition of centrosome amplification in cells depleted of Plk1 by siRNA.

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Cyclin-dependent kinase control of centrosome duplication

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Identification by targeted differential display of an immediate early gene encoding a putative serine/threonine kinase

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Phosphorylation at serine 75 is required for UV-mediated degradation of human Cdc25A phosphatase at the S-phase checkpoint

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Cell cycle regulation of the activity and subcellular localization of Plk1, a human protein kinase implicated in mitotic spindle function

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Dissociation of centrosome replication events from cycles of DNA synthesis and mitotic division in hydroxyurea-arrested Chinese hamster ovary cells

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Antibody microinjection reveals an essential role for human polo-like kinase 1 (Plk1) in the functional maturation of mitotic centrosomes

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Centriole disassembly in vivo and its effect on centrosome structure and function in vertebrate cells

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A centrosomal function for the human Nek2 protein kinase, a member of the NIMA family of cell cycle regulators.

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A system for stable expression of short interfering RNAs in mammalian cells

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Identification of an early-growth-response gene encoding a novel putative protein kinase

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Ectopic expression of Cdc25A accelerates the G(1)/S transition and leads to premature activation of cyclin E- and cyclin A-dependent kinases

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Silencing of the novel p53 target gene Snk/Plk2 leads to mitotic catastrophe in paclitaxel (taxol)-exposed cells

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Role of Plk2 (Snk) in mouse development and cell proliferation

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