School of Life Sciences, Swiss Institute for Experimental Cancer Research (ISREC), Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland.
School of Life Sciences, Swiss Institute for Experimental Cancer Research (ISREC), Swiss Federal Institute of Technology (EPFL), Lausanne, Switzerland
EMBO J. 2014 Aug 18;33(16):1815-30. doi: 10.15252/embj.201488147. Epub 2014 Jul 4.
The positioning and the elongation of the mitotic spindle must be carefully regulated. In human cells, the evolutionary conserved proteins LGN/Gαi1-3 anchor the coiled-coil protein NuMA and dynein to the cell cortex during metaphase, thus ensuring proper spindle positioning. The mechanisms governing cortical localization of NuMA and dynein during anaphase remain more elusive. Here, we report that LGN/Gαi1-3 are dispensable for NuMA-dependent cortical dynein enrichment during anaphase. We further establish that NuMA is excluded from the equatorial region of the cell cortex in a manner that depends on the centralspindlin components CYK4 and MKLP1. Importantly, we reveal that NuMA can directly associate with PtdInsP (PIP) and PtdInsP2 (PIP2) phosphoinositides in vitro. Furthermore, chemical or enzymatic depletion of PIP/PIP2 prevents NuMA cortical localization during mitosis, and conversely, increasing PIP2 levels augments mitotic cortical NuMA. Overall, our study uncovers a novel function for plasma membrane phospholipids in governing cortical NuMA distribution and thus the proper execution of mitosis.
有丝分裂纺锤体的定位和伸长必须仔细调节。在人类细胞中,进化保守的蛋白 LGN/Gαi1-3 在中期将卷曲螺旋蛋白 NuMA 和动力蛋白锚定在细胞膜皮质,从而确保纺锤体的正确定位。在后期,NuMA 和动力蛋白在细胞膜皮质的定位机制仍然更加难以捉摸。在这里,我们报告 LGN/Gαi1-3 对于后期依赖于 NuMA 的皮质动力蛋白富集是可有可无的。我们进一步证实,NuMA 以一种依赖于中心纺锤体成分 CYK4 和 MKLP1 的方式从细胞膜皮质的赤道区域被排除。重要的是,我们揭示了 NuMA 可以在体外直接与 PtdInsP(PIP)和 PtdInsP2(PIP2)磷脂酰肌醇结合。此外,化学或酶消耗 PIP/PIP2 会阻止有丝分裂期间 NuMA 的皮质定位,反之,增加 PIP2 水平会增加有丝分裂时皮质的 NuMA。总的来说,我们的研究揭示了质膜磷脂在调节皮质 NuMA 分布以及有丝分裂的正确执行中的新功能。