Time-lapse Imaging Reveals Dynamic Relocalization of PP1γ throughout the Mammalian Cell Cycle

Laura Trinkle-Mulcahy (Lead / Corresponding author), Paul D. Andrews, Sasala Wickramasinghe, Judith Sleeman, Alan Prescott, Yun Wah Lam, Carol Lyon, Jason R. Swedlow, Angus I. Lamond

    Research output: Contribution to journalArticle

    115 Citations (Scopus)

    Abstract

    Protein phosphatase 1 (PP1) is a ubiquitous serine/threonine phosphatase that regulates many cellular processes, including cell division. When transiently expressed as fluorescent protein (FP) fusions, the three PP1 isoforms, α, β/δ, and γ1, are active phosphatases with distinct localization patterns. We report here the establishment and characterization of HeLa cell lines stably expressing either FP-PP1γ or FP alone. Time-lapse imaging reveals dynamic targeting of FP-PP1γ to specific sites throughout the cell cycle, contrasting with the diffuse pattern observed for FP alone. FP-PP1γ shows a nucleolar accumulation during interphase. On entry into mitosis, it localizes initially at kinetochores, where it exchanges rapidly with the diffuse cytoplasmic pool. A dramatic relocalization of PP1 to the chromosome-containing regions occurs at the transition from early to late anaphase, and by telophase FP-PP1γ also accumulates at the cleavage furrow and midbody. The changing spatio-temporal distribution of PP1γ revealed using the stable PP1 cell lines implicates it in multiple processes, including nucleolar function, the regulation of chromosome segregation and cytokinesis.

    Original languageEnglish
    Pages (from-to)107-117
    Number of pages11
    JournalMolecular Biology of the Cell
    Volume14
    Issue number1
    DOIs
    Publication statusPublished - 1 Jan 2003

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