| Literature DB >> 27462074 |
Xiaogang Chu1, Xuanyu Chen2, Qingwen Wan2, Zhen Zheng2, Quansheng Du3.
Abstract
The large nuclear mitotic apparatus (NuMA) protein is an essential player in mitotic spindle assembly and maintenance. We report here the identification of Astrin, a spindle- and kinetochore-associated protein, as a novel interactor of NuMA. We show that the C-terminal tail of NuMA can directly bind to the C terminus of Astrin and that this interaction helps to recruit Astrin to microtubules. Knockdown of NuMA by RNA interference dramatically impaired Astrin recruitment to the mitotic spindle. Overexpression of the N terminus of mammalian homologue of Drosophila Pins (LGN), which blocks the microtubule binding of NuMA and competes with Astrin for NuMA binding, also led to similar results. Furthermore, we found that cytoplasmic dynein is required for the spindle pole accumulation of Astrin, and dynein-mediated transport is important for balanced distribution of Astrin between spindle poles and kinetochores. On the other hand, if Astrin levels are reduced, then NuMA could not efficiently concentrate at the spindle poles. Our findings reveal a direct physical link between two important regulators of mitotic progression and demonstrate the critical role of the NuMA-Astrin interaction for accurate cell division.Entities:
Keywords: Astrin; NuMA; chromosomes; microtubule; mitosis; mitotic spindle; protein-protein interaction
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Year: 2016 PMID: 27462074 PMCID: PMC5025691 DOI: 10.1074/jbc.M116.724831
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157