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Human Fidgetin is a microtubule severing the enzyme and minus-end depolymerase that regulates mitosis
Authors:Suranjana Mukherjee  J Daniel Diaz Valencia  Shannon Stewman  Jeremy Metz  Sylvain Monnier  Uttama Rath  Ana B Asenjo  Rabab A Charafeddine  Hernando J Sosa  Jennifer L Ross  Ao Ma  David J Sharp
Institution:1.Department of Physiology and Biophysics; Albert Einstein College of Medicine; Bronx, NY USA;2.Department of Physics; University of Massachusetts, Amherst; Amherst, MA USA
Abstract:Fidgetin is a member of the AAA protein superfamily with important roles in mammalian development. Here we show that human Fidgetin is a potent microtubule severing and depolymerizing the enzyme used to regulate mitotic spindle architecture, dynamics and anaphase A. In vitro, recombinant human Fidgetin severs taxol-stabilized microtubules along their length and promotes depolymerization, primarily from their minus-ends. In cells, human Fidgetin targets to centrosomes, and its depletion with siRNA significantly reduces the velocity of poleward tubulin flux and anaphase A chromatid-to-pole motion. In addition, the loss of Fidgetin induces a microtubule-dependent enlargement of mitotic centrosomes and an increase in the number and length of astral microtubules. Based on these data, we propose that human Fidgetin actively suppresses microtubule growth from and attachment to centrosomes.
Keywords:Fidgetin  centrosome  microtubule severing enzymes  microtubule-minus end depolymerase  mitosis  spindle
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