Messin Liam J, Millar Jonathan B A
Mechanochemical Cell Biology Building, Division of Biomedical Cell Biology, Warwick Medical School, University of Warwick, Gibbet Hill, Coventry, CV4 7AL UK.
Syst Synth Biol. 2014 Sep;8(3):205-13. doi: 10.1007/s11693-014-9140-z. Epub 2014 Mar 23.
Members of the kinesin-8 motor family play a central role in controlling microtubule length throughout the eukaryotic cell cycle. Inactivation of kinesin-8 causes defects in cell polarity during interphase and astral and mitotic spindle length, metaphase chromosome alignment, timing of anaphase onset and accuracy of chromosome segregation. Although the biophysical mechanism by which kinesin-8 molecules influence microtubule dynamics has been studied extensively in a variety of species, a consensus view has yet to emerge. One reason for this might be that some members of the kinesin-8 family can associate to other microtubule-associated proteins, cell cycle regulatory proteins and other kinesin family members. In this review we consider how cell cycle specific modification and its association to other regulatory proteins may modulate the function of kinesin-8 to enable it to function as a master regulator of microtubule dynamics.
驱动蛋白-8运动蛋白家族的成员在真核细胞周期中控制微管长度方面发挥着核心作用。驱动蛋白-8失活会导致间期细胞极性、星状和有丝分裂纺锤体长度、中期染色体排列、后期起始时间以及染色体分离准确性出现缺陷。尽管在多种物种中已广泛研究了驱动蛋白-8分子影响微管动力学的生物物理机制,但尚未形成共识观点。造成这种情况的一个原因可能是,驱动蛋白-8家族的一些成员可与其他微管相关蛋白、细胞周期调节蛋白及其他驱动蛋白家族成员结合。在本综述中,我们探讨细胞周期特异性修饰及其与其他调节蛋白的结合如何调节驱动蛋白-8的功能,使其能够作为微管动力学的主要调节因子发挥作用。