School of Biology, Indian Institute of Science Education and Research, CET Campus, Thiruvananthapuram, Kerala, India.
IUBMB Life. 2018 Feb;70(2):101-111. doi: 10.1002/iub.1708. Epub 2018 Jan 4.
Development and survival of all eukaryotic organisms depend on equal partitioning of their chromosomes between the two newly formed daughter cells during mitosis. The mitotic spindle performs the task of physically segregating the chromosomes through multiple stages of mitosis. During this process, kinetochore-microtubule attachment requires to be selectively stabilized to hold the chromosomes, but at the same time, it has to be flexible enough to allow kinetochore microtubule dynamicity and chromosome movements. Research during the last decade or so has identified a number of proteins associated with the spindle microtubule plus ends that regulate these processes and orchestrate forces to spatially organize and separate the chromosomes. In this review, we describe the molecular details of those regulators and their mechanisms of action at the kinetochore-microtubule interface. © 2018 IUBMB Life, 70(2):101-111, 2018.
所有真核生物的发育和生存都依赖于有丝分裂过程中染色体在两个新形成的子细胞之间的均等分配。有丝分裂纺锤体通过有丝分裂的多个阶段来完成物理分离染色体的任务。在此过程中,动粒微管附着需要选择性地稳定以固定染色体,但同时,它必须具有足够的灵活性,以允许动粒微管的动力学和染色体的运动。在过去十年左右的研究中,已经确定了许多与纺锤体微管正端相关的蛋白质,这些蛋白质调节这些过程,并协调力来空间组织和分离染色体。在这篇综述中,我们描述了那些调节剂的分子细节及其在动粒-微管界面上的作用机制。 © 2018 IUBMB Life,70(2):101-111,2018。