Cell cycle re-entry mechanisms after DNA damage checkpoints Giving it some gas to shut off the breaks!

Marcel A. T. M. van Vugt*, Michael B. Yaffe

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    21 Citations (Scopus)

    Abstract

    In order to maintain genetic integrity, cells are equipped with cell cycle checkpoints that detect DNA damage, orchestrate repair, and if necessary, eliminate severely damaged cells by inducing apoptotic cell death. The mitotic machinery is now emerging as an important determinant of the cellular responses to DNA damage where it functions as both the downstream target and the upstream regulator of the G(2)/M checkpoint. Cell cycle kinases and the DNA damage checkpoint kinases appear to reciprocally control each other. Specifically, cell cycle kinases control the inactivation of DNA damage checkpoint signaling. Termination of a DNA damage response by mitotic kinases appears to be an evolutionary conserved mechanism that allows resumption of cell cycle progression. Here we review recent reports in which molecular mechanisms underlying checkpoint silencing at the G(2)/M transition are elucidated.

    Original languageEnglish
    Pages (from-to)2097-2101
    Number of pages5
    JournalCell Cycle
    Volume9
    Issue number11
    Publication statusPublished - 1-Jun-2010

    Keywords

    • cell cycle checkpoint
    • DNA damage
    • Plk1
    • 53BP1
    • Chk2
    • mitosis
    • POLO-LIKE KINASE-1
    • DOUBLE-STRAND BREAK
    • SCF-BETA-TRCP
    • GENOMIC INSTABILITY
    • MITOTIC ENTRY
    • IONIZING-RADIATION
    • SOMATIC WEE1
    • G(1) ARREST
    • RECOVERY
    • ADAPTATION

    Fingerprint

    Dive into the research topics of 'Cell cycle re-entry mechanisms after DNA damage checkpoints Giving it some gas to shut off the breaks!'. Together they form a unique fingerprint.

    Cite this