Drosophila katanin is a microtubule depolymerase that regulates cortical-microtubule plus-end interactions and cell migration

被引:92
作者
Zhang, Dong [1 ]
Grode, Kyle D. [2 ,3 ]
Stewman, Shannon F. [1 ]
Diaz-Valencia, Juan Daniel [4 ]
Liebling, Emily [1 ]
Rath, Uttama [1 ]
Riera, Tania [1 ]
Currie, Joshua D. [2 ,3 ]
Buster, Daniel W. [5 ,6 ]
Asenjo, Ana B. [1 ]
Sosa, Hernando J. [1 ]
Ross, Jennifer L. [4 ]
Ma, Ao [1 ]
Rogers, Stephen L. [2 ,3 ]
Sharp, David J. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA
[2] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Ctr Carolina Genome Sci, Chapel Hill, NC 27599 USA
[4] Univ Massachusetts, Dept Phys, Amherst, MA 01003 USA
[5] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[6] Univ Arizona, Dept Cell Biol & Anat, Tucson, AZ 85724 USA
关键词
MITOTIC SPINDLE; DYNAMIC INSTABILITY; SEVERING PROTEINS; IN-VITRO; BINDING; MITOSIS; GROWTH; LENGTH; MELANOGASTER; ARCHITECTURE;
D O I
10.1038/ncb2206
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Regulation of microtubule dynamics at the cell cortex is important for cell motility, morphogenesis and division. Here we show that the Drosophila katanin Dm-Kat60 functions to generate a dynamic cortical-microtubule interface in interphase cells. Dm-Kat60 concentrates at the cell cortex of S2 Drosophila cells during interphase, where it suppresses the polymerization of microtubule plus-ends, there by preventing the formation of aberrantly dense cortical arrays. Dm-Kat60 also localizes at the leading edge of migratory D17 Drosophila cells and negatively regulates multiple parameters of their motility. Finally, in vitro, Dm-Kat60 severs and depolymerizes microtubules from their ends. On the basis of these data, we propose that Dm-Kat60 removes tubulin from microtubule lattice or microtubule ends that contact specific cortical sites to prevent stable and/or lateral attachments. The asymmetric distribution of such an activity could help generate regional variations in microtubule behaviours involved in cell migration.
引用
收藏
页码:361 / U71
页数:21
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