Zhao Xudong, D' Arca Domenico, Lim Wei Keat, Brahmachary Manisha, Carro Maria Stella, Ludwig Thomas, Cardo Carlos Cordon, Guillemot Francois, Aldape Ken, Califano Andrea, Iavarone Antonio, Lasorella Anna
Institute for Cancer Genetics, Columbia University Medical Center, New York, NY 10032, USA.
Dev Cell. 2009 Aug;17(2):210-21. doi: 10.1016/j.devcel.2009.07.009.
Self-renewal and proliferation of neural stem cells and the decision to initiate neurogenesis are crucial events directing brain development. Here we show that the ubiquitin ligase Huwe1 operates upstream of the N-Myc-DLL3-Notch pathway to control neural stem cell activity and promote neurogenesis. Conditional inactivation of the Huwe1 gene in the mouse brain caused neonatal lethality associated with disorganization of the laminar patterning of the cortex. These defects stemmed from severe impairment of neurogenesis associated with uncontrolled expansion of the neural stem cell compartment. Loss- and gain-of-function experiments in the mouse cortex demonstrated that Huwe1 restrains proliferation and enables neuronal differentiation by suppressing the N-Myc-DLL3 cascade. Notably, human high-grade gliomas carry focal hemizygous deletions of the X-linked Huwe1 gene in association with amplification of the N-myc locus. Our results indicate that Huwe1 balances proliferation and neurogenesis in the developing brain and that this pathway is subverted in malignant brain tumors.
神经干细胞的自我更新、增殖以及启动神经发生的决定是指导大脑发育的关键事件。我们在此表明,泛素连接酶Huwe1在N-Myc-DLL3-Notch通路的上游发挥作用,以控制神经干细胞活性并促进神经发生。小鼠大脑中Huwe1基因的条件性失活导致新生期致死,并伴有皮质层状结构紊乱。这些缺陷源于与神经干细胞池不受控制的扩张相关的神经发生严重受损。小鼠皮质中的功能丧失和功能获得实验表明,Huwe1通过抑制N-Myc-DLL3级联反应来抑制增殖并促进神经元分化。值得注意的是,人类高级别胶质瘤携带X连锁Huwe1基因的局灶性半合子缺失,并伴有N-myc基因座的扩增。我们的结果表明,Huwe1在发育中的大脑中平衡增殖和神经发生,并且该通路在恶性脑肿瘤中被颠覆。