Falnikar Aditi, Quintremil Sebastian, Zhao Hung-Jun, Cheng Haw-Yuan, Helmer Paige, Tsai Jin-Wu, Vallee Richard B
Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY 10032, USA.
Cell Rep. 2024 Dec 24;43(12):115008. doi: 10.1016/j.celrep.2024.115008. Epub 2024 Dec 11.
Radial glial progenitors (RGPs) are highly elongated epithelial cells that give rise to most stem cells, neurons, and glia in the vertebrate cerebral cortex. During development, the RGP nuclei exhibit a striking pattern of cell-cycle-dependent oscillatory movements known as interkinetic nuclear migration (INM), which we previously found to be mediated during G1 by the kinesin Kif1a and during G2 by cytoplasmic dynein, recruited to the nuclear envelope by the nucleoporins RanBP2 and Nup133. We now identify Nup153 as a nucleoporin anchor for Kif1a, responsible for G1-specific basal nuclear migration, providing a complete model for the mechanisms underlying this basic but mysterious behavior, with broad implications for understanding brain development.
放射状胶质祖细胞(RGPs)是高度伸长的上皮细胞,可产生脊椎动物大脑皮层中的大多数干细胞、神经元和神经胶质细胞。在发育过程中,RGP细胞核呈现出一种显著的细胞周期依赖性振荡运动模式,称为核内运动(INM),我们之前发现,在G1期由驱动蛋白Kif1a介导,在G2期由细胞质动力蛋白介导,通过核孔蛋白RanBP2和Nup133募集到核膜。我们现在确定Nup153是Kif1a的核孔蛋白锚定物,负责G1期特异性的基底核迁移,为这种基本但神秘行为的潜在机制提供了一个完整模型,对理解大脑发育具有广泛意义。