PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody
Author: ["Antonia P. Sagona","Ioannis P. Nezis","Nina Marie Pedersen","Knut Liestøl","John Poulton","Tor Erik Rusten","Rolf I. Skotheim","Camilla Raiborg","Harald Stenmark"]
Publication: Nature Cell Biology
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Abstract
A new link is reported between regulators of endosomal trafficking and cytokinesis. Production of the phosphoinositide lipid PI3P at the midbody triggers the KIF13A-mediated recruitment of the centrosomal proteins FYVE-CENT and TTC19 to the division site. TTC19 may in turn regulate abscission by control of the ESCRTIII complex. Several subunits of the class III phosphatidylinositol-3-OH kinase (PI(3)K-III) complex are known as tumour suppressors. Here we uncover a function for this complex and its catalytic product phosphatidylinositol-3-phosphate (PtdIns(3)P) in cytokinesis. We show that PtdIns(3)P localizes to the midbody during cytokinesis and recruits a centrosomal protein, FYVE-CENT (ZFYVE26), and its binding partner TTC19, which in turn interacts with CHMP4B, an endosomal sorting complex required for transport (ESCRT)-III subunit implicated in the abscission step of cytokinesis. Translocation of FYVE-CENT and TTC19 from the centrosome to the midbody requires another FYVE-CENT-interacting protein, the microtubule motor KIF13A. Depletion of the VPS34 or Beclin 1 subunits of PI(3)K-III causes cytokinesis arrest and an increased number of binucleate and multinucleate cells, in a similar manner to the depletion of FYVE-CENT, KIF13A or TTC19. These results provide a mechanism for the translocation and docking of a cytokinesis regulatory machinery at the midbody.
Cite this article
Sagona, A., Nezis, I., Pedersen, N. et al. PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody. Nat Cell Biol 12, 362–371 (2010). https://doi.org/10.1038/ncb2036
