Dissecting Temporal and Spatial Control of Cytokinesis with a Myosin II Inhibitor

Author:

Straight Aaron F.1,Cheung Amy1,Limouze John2,Chen Irene3,Westwood Nick J.4,Sellers James R.2,Mitchison Timothy J.1

Affiliation:

1. Department of Cell Biology and Institute of Chemistry and Cell Biology, Harvard Medical School, 250 Longwood Avenue, Boston, MA 02115, USA.

2. Laboratory of Molecular Cardiology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.

3. Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.

4. School of Chemistry, University of St. Andrews, St. Andrews, Fife, KY16 9AJ, UK.

Abstract

Completion of cell division during cytokinesis requires temporally and spatially regulated communication from the microtubule cytoskeleton to the actin cytoskeleton and the cell membrane. We identified a specific inhibitor of nonmuscle myosin II, blebbistatin, that inhibited contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly. Using blebbistatin and other drugs, we showed that exit from the cytokinetic phase of the cell cycle depends on ubiquitin-mediated proteolysis. Continuous signals from microtubules are required to maintain the position of the cleavage furrow, and these signals control the localization of myosin II independently of other furrow components.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference34 articles.

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