Department of Physiology and Biophysics, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York 10461, USA.
Nat Cell Biol. 2011 Apr;13(4):361-70. doi: 10.1038/ncb2206. Epub 2011 Mar 6.
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, thereby 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.
细胞皮层处微管动力学的调节对于细胞运动、形态发生和分裂很重要。在这里,我们发现果蝇katanin Dm-Kat60 可以在间期细胞中产生动态的皮层-微管界面。在间期的 S2 果蝇细胞中,Dm-Kat60 集中在细胞膜皮层上,抑制微管正端的聚合,从而防止异常密集的皮层排列的形成。Dm-Kat60 还定位于迁移的 D17 果蝇细胞的前缘,并负调控它们运动的多个参数。最后,在体外,Dm-Kat60 从微管末端切割和去聚合微管。基于这些数据,我们提出 Dm-Kat60 从与特定皮层位点接触的微管晶格或微管末端去除微管蛋白,以防止稳定和/或横向附着。这种活性的不对称分布有助于产生参与细胞迁移的微管行为的区域变化。