Human fidgetin is a microtubule severing enzyme and minus-end depolymerase that regulates mitosis

被引:51
作者
Mukherjee, Suranjana [1 ]
Valencia, J. Daniel Diaz [2 ]
Stewman, Shannon [1 ]
Metz, Jeremy [1 ]
Monnier, Sylvain [1 ]
Rath, Uttama [1 ]
Asenjo, Ana B. [1 ]
Charafeddine, Rabab A. [1 ]
Sosa, Hernando J. [1 ]
Ross, Jennifer L. [2 ]
Ma, Ao [1 ]
Sharp, David J. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10467 USA
[2] Univ Massachusetts, Dept Phys, Amherst, MA 01003 USA
关键词
fidgetin; centrosome; microtubule severing enzymes; microtubule-minus end depolymerase; mitosis; spindle; AAA PROTEINS; KATANIN; ATPASE; MOUSE; FLUX;
D O I
10.4161/cc.20849
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 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.
引用
收藏
页码:2359 / 2366
页数:8
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