Tanenbaum Marvin E, Medema René H, Akhmanova Anna
Department of Medical Oncology and Cancer Genomics Center; University Medical Center; Utrecht, The Netherlands.
Bioarchitecture. 2011 Mar;1(2):80-87. doi: 10.4161/bioa.1.2.15807.
Mitotic Centromere Associated Kinesin (MCAK) is a potent microtubule depolymerizing and catastrophe-inducing factor, which uses the energy of ATP hydrolysis to destabilize microtubule ends. MCAK is localized to inner centromeres, kinetochores and spindle poles of mitotic cells, and is also present in the cytoplasm. Both in interphase and in mitosis, MCAK can specifically accumulate at the growing microtubule ends. Here we discuss the mechanisms, which modulate subcellular localization and activity of MCAK through the interaction with the End Binding (EB) proteins and phosphorylation.
有丝分裂着丝粒相关驱动蛋白(MCAK)是一种强大的微管解聚和诱导微管灾变因子,它利用ATP水解产生的能量使微管末端不稳定。MCAK定位于有丝分裂细胞的内着丝粒、动粒和纺锤体极,也存在于细胞质中。在间期和有丝分裂期,MCAK都能特异性地聚集在生长中的微管末端。在此,我们讨论通过与末端结合(EB)蛋白相互作用和磷酸化来调节MCAK亚细胞定位和活性的机制。