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Published October 18, 2011 | Published + Supplemental Material
Journal Article Open

Rab5 GTPase controls chromosome alignment through Lamin disassembly and relocation of the NuMA-like protein Mud to the poles during mitosis

Abstract

The small GTPase Rab5 is a conserved regulator of membrane trafficking; it regulates the formation of early endosomes, their transport along microtubules, and the fusion to the target organelles. Although several members of the endocytic pathway were recently implicated in spindle organization, it is unclear whether Rab5 has any role during mitosis. Here, we describe that Rab5 is required for proper chromosome alignment during Drosophila mitoses. We also found that Rab5 associated in vivo with nuclear Lamin and mushroom body defect (Mud), the Drosophila counterpart of nuclear mitotic apparatus protein (NuMA). Consistent with this finding, Rab5 was required for the disassembly of the nuclear envelope at mitotic entry and the accumulation of Mud at the spindle poles. Furthermore, Mud depletion caused chromosome misalignment defects that resembled the defects of Rab5 RNAi cells, and double-knockdown experiments indicated that the two proteins function in a linear pathway. Our results indicate a role for Rab5 in mitosis and reinforce the emerging view of the contributions made by cell membrane dynamics to spindle function.

Additional Information

© 2011 National Academy of Sciences. Edited by Pietro De Camilli, Yale University and The Howard Hughes Medical Institute, New Haven, CT, and approved September 7, 2011 (received for review March 9, 2011) We thank Letizia Lanzetti for sharing unpublished results; T. S. Hays, H. A. Nash, P. G. Wilson, M. S. Savoian, T. Takeda, V. Korolchuk, and M. Gonzalez-Gaitan for reagents; P. Lió for statistical advice, T. Maresca for his 3F3/2 antibody staining protocol, and P. Almeida Coelho for help with image deconvolution; and M. S. Savoian, P. Almeida Coelho, T. Takeda, and E. Wegel for critical reading of the manuscript and all D.M.G. laboratory members (past and present) for invaluable discussions throughout this work. This research was supported in part by grants from the Biotechnology and Biological Sciences Research Council Link and Cancer Research United Kingdom Programme (to D.M.G.). V.A. was a Human Frontier Science Program fellow. Author contributions: L.C., P.P.D., and D.M.G. designed research; L.C., P.P.D., and V.A. performed research; L.C. and D.M.G. analyzed data; and L.C., P.P.D., and D.M.G. wrote the paper. The authors declare no conflict of interest. This article is a PNAS Direct Submission. This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1103720108/-/DCSupplemental.

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Published - 17343.full.pdf

Supplemental Material - pnas.201103720SI.pdf

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