Department of Experimental Oncology, European Institute of Oncology, Via Adamello 16, 20139, Milano, Italy.
Diamond Light Source Ltd., Diamond House, Harwell Science and Innovation Campus, Chilton, Didcot, Oxfordshire, OX11 0DE, UK.
Nat Commun. 2018 Mar 9;9(1):1025. doi: 10.1038/s41467-018-03343-4.
Asymmetric cell divisions balance stem cell proliferation and differentiation to sustain tissue morphogenesis and homeostasis. During asymmetric divisions, fate determinants and niche contacts segregate unequally between daughters, but little is known on how this is achieved mechanistically. In Drosophila neuroblasts and murine mammary stem cells, the association of the spindle orientation protein LGN with the stem cell adaptor Inscuteable has been connected to asymmetry. Here we report the crystal structure of Drosophila LGN in complex with the asymmetric domain of Inscuteable, which reveals a tetrameric arrangement of intertwined molecules. We show that Insc:LGN tetramers constitute stable cores of Par3-Insc-LGN-Gαi complexes, which cannot be dissociated by NuMA. In mammary stem cells, the asymmetric domain of Insc bound to LGN:Gαi suffices to drive asymmetric fate, and reverts aberrant symmetric divisions induced by p53 loss. We suggest a novel role for the Insc-bound pool of LGN acting independently of microtubule motors to promote asymmetric fate specification.
不对称细胞分裂平衡干细胞增殖和分化,以维持组织形态发生和动态平衡。在不对称分裂中,命运决定因素和生态位接触在子细胞之间不均匀地分离,但对于如何在机制上实现这一点知之甚少。在果蝇神经母细胞和鼠乳腺干细胞中,纺锤体定向蛋白 LGN 与干细胞衔接蛋白 Inscuteable 的关联与不对称性有关。在这里,我们报告了果蝇 LGN 与 Inscuteable 的不对称结构域的晶体结构,揭示了分子相互交织的四聚体排列。我们表明,Insc:LGN 四聚体构成了 Par3-Insc-LGN-Gαi 复合物的稳定核心,NuMA 不能将其解离。在乳腺干细胞中,与 LGN:Gαi 结合的 Insc 不对称结构域足以驱动不对称命运,并逆转由 p53 缺失引起的异常对称分裂。我们提出了一个新的作用,即 Insc 结合的 LGN 池独立于微管马达作用,以促进不对称命运的指定。