Probing Spindle Assembly Mechanisms with Monastrol, a Small Molecule Inhibitor of the Mitotic Kinesin, Eg5

Monastrol, a cell-permeable small molecule inhibitor of the mitotic kinesin, Eg5, arrests cells in mitosis with monoastral spindles. Here, we use monastrol to probe mitotic mechanisms. We find that monastrol does not inhibit progression through S and G2 phases of the cell cycle or centrosome duplication. The mitotic arrest due to monastrol is also rapidly reversible. Chromosomes in monastrol-treated cells frequently have both sister kinetochores attached to microtubules extending to the center of the monoaster (syntelic orientation). Mitotic arrest–deficient protein 2 (Mad2) localizes to a subset of kinetochores, suggesting the activation of the spindle assembly checkpoint in these cells. Mad2 localizes to some kinetochores that have attached microtubules in monastrol-treated cells, indicating that kinetochore microtubule attachment alone may not satisfy the spindle assembly checkpoint. Monastrol also inhibits bipolar spindle formation in Xenopus egg extracts. However, it does not prevent the targeting of Eg5 to the monoastral spindles that form. Imaging bipolar spindles disassembling in the presence of monastrol allowed direct observations of outward directed forces in the spindle, orthogonal to the pole-to-pole axis. Monastrol is thus a useful tool to study mitotic processes, detection and correction of chromosome malorientation, and contributions of Eg5 to spindle assembly and maintenance.

[1]  C. Rieder,et al.  Reproductive capacity of sea urchin centrosomes without centrioles. , 1989, Cell motility and the cytoskeleton.

[2]  H. Lane,et al.  Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo , 1995, Cell.

[3]  C. Rieder,et al.  Chromosome mal-orientation and reorientation during mitosis. , 1992, Cell motility and the cytoskeleton.

[4]  D. Dujardin,et al.  Dynein and dynactin are localized to astral microtubules and at cortical sites in mitotic epithelial cells , 1998, Current Biology.

[5]  E. Taylor,et al.  ISOLATION OF A PROTEIN SUBUNIT FROM MICROTUBULES , 1967, The Journal of cell biology.

[6]  C. Rieder The formation, structure, and composition of the mammalian kinetochore and kinetochore fiber. , 1982, International review of cytology.

[7]  Nicklas Rb How Cells Get the Right Chromosomes , 1997, Science.

[8]  R. Nicklas How Cells Get the Right Chromosomes , 1997, Science.

[9]  M. Hoyt,et al.  Mitotic motors in Saccharomyces cerevisiae. , 2000, Biochimica et biophysica acta.

[10]  S. Kuo,et al.  Motile Properties of the Kinesin-related Cin8p Spindle Motor Extracted from Saccharomyces cerevisiae Cells* , 1999, The Journal of Biological Chemistry.

[11]  T. Mitchison,et al.  Poleward Microtubule Flux in Mitotic Spindles Assembled in Vitro , 2002 .

[12]  I. Vernos,et al.  A model for the proposed roles of different microtubule-based motor proteins in establishing spindle bipolarity , 1998, Current Biology.

[13]  A. Murray,et al.  Localization of Mad2 to Kinetochores Depends on Microtubule Attachment, Not Tension , 1998, The Journal of cell biology.

[14]  Andrew W. Murray,et al.  Association of Spindle Assembly Checkpoint Component XMAD2 with Unattached Kinetochores , 1996, Science.

[15]  A. Hyman,et al.  Preparation of modified tubulins. , 1991, Methods in enzymology.

[16]  A. Murray,et al.  Real time observation of anaphase in vitro. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[17]  K. Ramyar,et al.  A Complex of NuMA and Cytoplasmic Dynein Is Essential for Mitotic Spindle Assembly , 1996, Cell.

[18]  T. Mitchison,et al.  Towards a pharmacological genetics. , 1994, Chemistry & biology.

[19]  A. Murray,et al.  The use of Xenopus egg extracts to study mitotic spindle assembly and function in vitro. , 1999, Methods in cell biology.

[20]  P. Meluh,et al.  Kinesin-related proteins required for assembly of the mitotic spindle , 1992, The Journal of cell biology.

[21]  G. Borisy,et al.  THE MECHANISM OF ACTION OF COLCHICINE , 1967, The Journal of cell biology.

[22]  Y. Fukui,et al.  Reorganization of microtubules during mitosis in Dictyostelium: Dissociation from MTOC and selective assembly/disassembly in situ , 1987 .

[23]  Dana L. Miller,et al.  Novel Roles for Saccharomyces cerevisiae Mitotic Spindle Motors , 1999, The Journal of cell biology.

[24]  M. Yanagida,et al.  Kinesin-related cut 7 protein associates with mitotic and meiotic spindles in fission yeast , 1992, Nature.

[25]  B. Roberts,et al.  S. cerevisiae genes required for cell cycle arrest in response to loss of microtubule function , 1991, Cell.

[26]  G. Schatten,et al.  The Kinesin-Related Protein, Hset, Opposes the Activity of Eg5 and Cross-Links Microtubules in the Mammalian Mitotic Spindle , 1999, The Journal of cell biology.

[27]  D. Agard,et al.  Fluorescence microscopy in three dimensions. , 1989, Methods in cell biology.

[28]  A. Spradling,et al.  The kinesin-like protein KLP61F is essential for mitosis in Drosophila , 1993, The Journal of cell biology.

[29]  M. Hoyt,et al.  Kinesin-related proteins required for structural integrity of the mitotic spindle , 1992, Cell.

[30]  R. Benezra,et al.  Identification of a Human Mitotic Checkpoint Gene: hsMAD2 , 1996, Science.

[31]  Stephen S. Taylor,et al.  Kinetochore Localization of Murine Bub1 Is Required for Normal Mitotic Timing and Checkpoint Response to Spindle Damage , 1997, Cell.

[32]  E. Salmon,et al.  The vertebrate cell kinetochore and its roles during mitosis. , 1998, Trends in Cell Biology.

[33]  Timothy J. Mitchison,et al.  Mitotic spindle organization by a plus-end-directed microtubule motor , 1992, Nature.

[34]  M. Yanagida,et al.  Novel potential mitotic motor protein encoded by the fission yeast cut7+ gene , 1990, Nature.

[35]  N. Morris,et al.  Mutation of a gene that encodes a kinesin-like protein blocks nuclear division in A. nidulans , 1990, Cell.

[36]  S Inoué,et al.  1. EARLY HISTORY: THE DYNAMIC EQUILIBRIUM MODEL , 1995 .

[37]  Alexey Khodjakov,et al.  Centrosome-independent mitotic spindle formation in vertebrates , 2000, Current Biology.

[38]  G. Gorbsky,et al.  Kinetochore chemistry is sensitive to tension and may link mitotic forces to a cell cycle checkpoint , 1995, The Journal of cell biology.

[39]  Andrew W. Murray,et al.  Feedback control of mitosis in budding yeast , 1991, Cell.

[40]  K. Loo,et al.  Two Saccharomyces cerevisiae kinesin-related gene products required for mitotic spindle assembly , 1992, The Journal of cell biology.

[41]  E. Nigg,et al.  Phosphorylation by p34cdc2 Protein Kinase Regulates Binding of the Kinesin-related Motor HsEg5 to the Dynactin Subunit p150Glued * , 1997, The Journal of Biological Chemistry.

[42]  M. Winey,et al.  MPS1 and MPS2: novel yeast genes defining distinct steps of spindle pole body duplication , 1991, The Journal of cell biology.

[43]  M. Kirschner,et al.  Sites of microtubule assembly and disassembly in the mitotic spindle , 1986, Cell.

[44]  E D Salmon,et al.  Motile kinetochores and polar ejection forces dictate chromosome position on the vertebrate mitotic spindle , 1994, The Journal of cell biology.

[45]  T. Mitchison,et al.  Polewards microtubule flux in the mitotic spindle: evidence from photoactivation of fluorescence , 1989, The Journal of cell biology.

[46]  J. Scholey,et al.  Antagonistic microtubule-sliding motors position mitotic centrosomes in Drosophila early embryos , 1999, Nature Cell Biology.