Literature DB >> 16682204

Cdc25: mechanisms of checkpoint inhibition and recovery.

Christina Karlsson-Rosenthal1, Jonathan B A Millar.   

Abstract

Members of the eukaryotic Cdc25 phosphatase family are key targets of the Chk1 and Chk2 checkpoint kinases, which inactivate Cdc25 to halt cell cycle progression when DNA is damaged or incompletely replicated. Now, new kinases that phosphorylate and inactivate Cdc25 are being discovered, including MAPKAP kinase-2, a component of the p38 stress-activated MAP kinase pathway. The roles of other kinases, such as cyclin-dependent kinase, Polo and Aurora A kinase, in controlling the localization or the activation of Cdc25, are controversial. Here, we discuss new data that suggests that different Cdc25 isoforms and regulators of Cdc25 are differentially required for normal cell cycle progression and recovery from checkpoint arrest.

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Year:  2006        PMID: 16682204     DOI: 10.1016/j.tcb.2006.04.002

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  97 in total

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2.  Arabidopsis T-DNA insertional lines for CDC25 are hypersensitive to hydroxyurea but not to zeocin or salt stress.

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Review 3.  Centrosomes in the DNA damage response--the hub outside the centre.

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Journal:  Chromosome Res       Date:  2016-01       Impact factor: 5.239

4.  Down-regulation of CK2 activity results in a decrease in the level of cdc25C phosphatase in different prostate cancer cell lines.

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Journal:  Mol Cell Biochem       Date:  2011-07-13       Impact factor: 3.396

5.  Female infertility in PDE3A(-/-) mice: polo-like kinase 1 (Plk1) may be a target of protein kinase A (PKA) and involved in meiotic arrest of oocytes from PDE3A(-/-) mice.

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6.  Regulated activity of PP2A-B55 delta is crucial for controlling entry into and exit from mitosis in Xenopus egg extracts.

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7.  Genotoxic stress modulates CDC25C phosphatase alternative splicing in human breast cancer cell lines.

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Review 8.  In vivo roles of CDC25 phosphatases: biological insight into the anti-cancer therapeutic targets.

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Journal:  Anticancer Agents Med Chem       Date:  2008-12       Impact factor: 2.505

9.  Multiplexed random peptide library and phospho-specific antibodies facilitate human polo-like kinase 1 inhibitor screen.

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