Mishima Masanori, Kaitna Susanne, Glotzer Michael
Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, A-1030, Vienna, Austria.
Dev Cell. 2002 Jan;2(1):41-54. doi: 10.1016/s1534-5807(01)00110-1.
A late step in cytokinesis requires the central spindle, which forms during anaphase by the bundling of antiparallel nonkinetochore microtubules. Microtubule bundling and completion of cytokinesis require ZEN-4/CeMKLP-1, a kinesin-like protein, and CYK-4, which contains a RhoGAP domain. We show that CYK-4 and ZEN-4 exist in a complex in vivo that can be reconstituted in vitro. The N terminus of CYK-4 binds the central region of ZEN-4, including the neck linker. Genetic suppression data prove the functional significance of this interaction. An analogous complex, containing equimolar amounts of a CYK-4 ortholog and MKLP-1, was purified from mammalian cells. Biochemical studies indicate that this complex, named centralspindlin, is a heterotetramer. Centralspindlin, but not its individual components, strongly promotes microtubule bundling in vitro.
胞质分裂的最后一步需要中心纺锤体,它在后期通过反平行非动粒微管的束集而形成。微管束集和胞质分裂的完成需要ZEN-4/CeMKLP-1(一种驱动蛋白样蛋白)和含有RhoGAP结构域的CYK-4。我们发现CYK-4和ZEN-4在体内以复合物形式存在,且该复合物可在体外重组。CYK-4的N端结合ZEN-4的中心区域,包括颈部连接区。基因抑制数据证明了这种相互作用的功能重要性。从哺乳动物细胞中纯化出了一种类似的复合物,其含有等摩尔量的CYK-4直系同源物和MKLP-1。生化研究表明,这种名为中心纺锤体蛋白的复合物是一种异源四聚体。中心纺锤体蛋白而非其单个组分,在体外能强力促进微管束集。