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Originally published as MBC in Press, 10.1091/mbc.E04-10-0927 on December 15, 2004

Vol. 16, Issue 2, 849-860, February 2005

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The FIP3-Rab11 Protein Complex Regulates Recycling Endosome Targeting to the Cleavage Furrow during Late Cytokinesis{boxd}{boxv}

Gayle M. Wilson * {dagger}, Andrew B. Fielding {dagger} {ddagger}, Glenn C. Simon *, Xinzi Yu {ddagger}, Paul D. Andrews §, Rebecca S. Hames  ||, Andrew M. Frey  ||, Andrew A. Peden ¶, Gwyn W. Gould {ddagger}, and Rytis Prekeris *

* Department of Cellular and Developmental Biology, School of Medicine, University of Colorado Health Sciences Center, Denver, CO 80262; {ddagger} The Henry Wellcome Laboratory of Cell Biology, Division of Biochemistry and Molecular Biology, Faculty of Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom; § Division of Gene Regulation and Expression, Wellcome Trust Biocentre, University of Dundee, Dundee DD1 5EH, United Kingdom; || Department of Biochemistry, University of Leicester, Leicester LE1 7RH, United Kingdom; and Genentech, South San Francisco, CA 94080-4990

Submitted October 26, 2004; Revised November 17, 2004; Accepted November 18, 2004
Monitoring Editor: Jean Gruenberg

An integral part of cell division is the separation of daughter cells via cytokinesis. There is now good evidence that the completion of cytokinesis requires coordinated membrane trafficking to deliver new membrane to the tip of the furrow and to complete the abscission. Here we have examined membrane traffic in cytokinesis and describe several novel observations. First, we show that Rab11- and FIP3-containing recycling endosomes accumulate near the cleavage furrow and are required for successful completion of cytokinesis. Second, we demonstrate that the Rab11-FIP3 protein complex is intimately involved in the delivery of endosomes to the cleavage furrow. Significantly, although FIP3 recruitment to endosomes is Rab11 dependent, we find that the targeting of FIP3 to the midbody is independent of Rab11. Third, we show that the Rab11-FIP3 complex is required for a late stage of cytokinesis, possibly abscission. Finally, we demonstrate that localization of FIP3 is subject to substantial spatial and temporal regulation. These data provide the first detailed analysis of recycling endosomes in cell division and provide a new model for membrane traffic to the furrow. We propose that the dynamic Rab11-FIP3 interaction controls the delivery, targeting, and fusion of recycling endosomes with furrow during late cytokinesis and abscission.


Article published online ahead of print in MBC in Press on December 15, 2004 (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E04-10-0927).

{boxd}{boxv} The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).

{dagger} These authors contributed equally to this work.

Address correspondence to: Rytis Prekeris (Rytis.Prekeris{at}uchsc.edu) or Gwyn W. Gould (G.Gould{at}bio.gla.ac.uk).




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