A novel role for clathrin in cytokinesis

  1. Maria L. Niswonger and
  2. Theresa J. O’Halloran*
  1. Department of Cell Biology, Box 3709, Duke University Medical Center, Durham, NC 27710

Abstract

Using clathrin-minus Dictyostelium cells, we identified a novel requirement for clathrin during cytokinesis. In suspension culture, clathrin-minus cells failed to divide and became large and multinucleate. This cytokinesis deficiency was not attributable to a pleiotropic effect on the actomyosin cytoskeleton, since other cellular events driven by myosin II (e.g., cortical contraction and capping of concanavalin A receptors) remained intact in clathrin-minus cells. Examination of cells expressing myosin II tagged with green fluorescent protein showed that clathrin-minus cells failed to assemble myosin II into a functional contractile ring. This inability to localize myosin II to a particular location was specific for cytokinesis, since clathrin-minus cells moving across a substrate localized myosin II properly to their posterior cortexes. These results demonstrate that clathrin is essential for construction of a functional contractile ring during cell division.

Footnotes

  • * To whom reprint requests should be addressed. e-mail: t.o’halloran{at}cellbio.duke.edu.

  • James A. Spudich, Stanford University, Stanford, CA

  • ABBREVIATIONS:
    Con A,
    concanavalin A;
    DAPI,
    4,6-diamidino-2-phenylindole;
    gfp,
    green fluorescent protein
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