Deregulated human Cdc14A phosphatase disrupts centrosome separation and chromosome segregation

Research output: Contribution to journalJournal articleResearchpeer-review

We show that human Cdc14A phosphatase interacts with interphase centrosomes, and that this interaction is independent of microtubules and Cdc14A phosphatase activity, but requires active nuclear export. Disrupting the nuclear export signal (NES) led to Cdc14A being localized in nucleoli, which in unperturbed cells selectively contain Cdc14B (ref. 1). Conditional overproduction of Cdc14A, but not its phosphatase-dead or NES-deficient mutants, or Cdc14B, resulted in premature centrosome splitting and formation of supernumerary mitotic spindles. In contrast, downregulation of endogenous Cdc14A by short inhibitory RNA duplexes (siRNA) induced mitotic defects including impaired centrosome separation and failure to undergo productive cytokinesis. Consequently, both overexpression and downregulation of Cdc14A caused aberrant chromosome partitioning into daughter cells. These results indicate that Cdc14A is a physiological regulator of the centrosome duplication cycle, which, when disrupted, can lead to genomic instability in mammalian cells.

Original languageEnglish
JournalNature Cell Biology
Issue number4
Pages (from-to)317-22
Number of pages6
Publication statusPublished - Apr 2002
Externally publishedYes

    Research areas

  • Cell Cycle Proteins, Cell Division, Cell Line, Cell Nucleus, Centrosome, Chromosomes, Down-Regulation, Flow Cytometry, HeLa Cells, Humans, Immunoblotting, Kinetics, Microscopy, Fluorescence, Microtubules, Mitosis, Mutation, Phosphoric Monoester Hydrolases, Plasmids, Protein Tyrosine Phosphatases, RNA, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Schizosaccharomyces, Time Factors, Transgenes

ID: 124904249