Kiyomitsu Tomomi, Boerner Susan
Cell Division Dynamics Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Japan.
Front Cell Dev Biol. 2021 Apr 1;9:653801. doi: 10.3389/fcell.2021.653801. eCollection 2021.
The nuclear mitotic apparatus (NuMA) protein is well conserved in vertebrates, and dynamically changes its subcellular localization from the interphase nucleus to the mitotic/meiotic spindle poles and the mitotic cell cortex. At these locations, NuMA acts as a key structural hub in nuclear formation, spindle assembly, and mitotic spindle positioning, respectively. To achieve its variable functions, NuMA interacts with multiple factors, including DNA, microtubules, the plasma membrane, importins, and cytoplasmic dynein. The binding of NuMA to dynein via its N-terminal domain drives spindle pole focusing and spindle positioning, while multiple interactions through its C-terminal region define its subcellular localizations and functions. In addition, NuMA can self-assemble into high-ordered structures which likely contribute to spindle positioning and nuclear formation. In this review, we summarize recent advances in NuMA's domains, functions and regulations, with a focus on human NuMA, to understand how and why vertebrate NuMA participates in these functions in comparison with invertebrate NuMA-related proteins.
核有丝分裂装置(NuMA)蛋白在脊椎动物中高度保守,其亚细胞定位会从间期细胞核动态变化至有丝分裂/减数分裂纺锤体极以及有丝分裂细胞皮层。在这些位置,NuMA分别在核形成、纺锤体组装和有丝分裂纺锤体定位过程中扮演关键的结构枢纽角色。为实现其多样功能,NuMA会与多种因子相互作用,包括DNA、微管、质膜、输入蛋白和胞质动力蛋白。NuMA通过其N端结构域与动力蛋白结合,驱动纺锤体极聚焦和纺锤体定位,而通过其C端区域的多种相互作用则决定了其亚细胞定位和功能。此外,NuMA能够自组装成高阶结构,这可能有助于纺锤体定位和核形成。在本综述中,我们总结了NuMA结构域、功能和调控方面的最新进展,重点关注人类NuMA,以了解与无脊椎动物NuMA相关蛋白相比,脊椎动物NuMA如何以及为何参与这些功能。