Department of Neuroscience and Cell Biology, University of Texas Medical Branch School of Medicine, Galveston, TX 77555, USA.
Dev Biol. 2011 Mar 1;351(1):186-98. doi: 10.1016/j.ydbio.2010.12.008. Epub 2010 Dec 11.
In the CNS, the evolutionarily conserved Notch pathway regulates asymmetric cell fate specification to daughters of ganglion mother cells (GMCs). The E3 Ubiquitin ligase protein Neuralized (Neur) is thought to activate Notch-signaling by the endocytosis of Delta and the Delta-bound extracellular domain of Notch. The intracellular Notch then initiates Notch-signaling. Numb blocks N-signaling in one of the two daughters of a GMC, allowing that cell to adopt a different identity. Numb is asymmetrically localized in a GMC and is segregated to only one of the two daughter cells. In the typical GMC-1→RP2/sib lineage, we found that loss of Neur activity causes symmetric division of GMC-1 into two RP2s. We further found that Neur asymmetrically localizes in a late GMC-1 to the Numb domain and Neur mediates asymmetric division via two distinct, sequential mechanisms: by promoting the asymmetric localization of Numb in a GMC-1 via down-regulation of the transcription factor Pdm1, followed by enhancing the Notch-signaling via trans-potentiation of Notch in a cell committed to become a sib. In neur mutants the GMC-1 identity is not altered but Numb is non-asymmetrically localized due to an up-regulation of Pdm1. Thus, both its daughters inherit Numb, which prevents Notch from specifying a sib identity. Neur also enhances Notch since in neur; numb double mutants, both sibling cells often adopt a mixed fate as opposed to an RP2 fate observed in Notch; numb double mutants. Furthermore, over-expression of Neur can induce both cells to adopt a sib fate similar to gain of function Notch. Our results tie Numb and Notch-signaling through a single player, Neur, thus giving us a more complete picture of the events surrounding asymmetric division of precursor cells. We also show that Neur and Numb are interdependent for their asymmetric-localizations.
在中枢神经系统中,进化上保守的 Notch 途径调节神经母细胞(GMC)的女儿的不对称细胞命运决定。E3 泛素连接酶蛋白 Neuralized(Neur)被认为通过内吞作用 Delta 和 Notch 的 Delta 结合的细胞外结构域来激活 Notch 信号。然后,细胞内 Notch 启动 Notch 信号。Numb 在 GMC 的两个女儿之一中阻断 N 信号,使该细胞采用不同的身份。Numb 在 GMC 中不对称定位,并仅分配给两个子细胞之一。在典型的 GMC-1→RP2/sib 谱系中,我们发现 Neur 活性的丧失导致 GMC-1 对称分裂为两个 RP2。我们进一步发现,Neur 在晚期 GMC-1 中不对称地定位于 Numb 域,并且 Neur 通过两种不同的、连续的机制介导不对称分裂:通过下调转录因子 Pdm1 促进 GMC-1 中 Numb 的不对称定位,随后通过在一个细胞中增强 Notch 信号增强 Notch,该细胞被承诺成为 sib。在 neur 突变体中,GMC-1 身份没有改变,但由于 Pdm1 的上调,Numb 是非不对称定位的。因此,它的两个女儿都继承了 Numb,这阻止了 Notch 指定 sib 身份。Neur 还增强了 Notch,因为在 neur;numb 双突变体中,两个 sib 细胞通常采用混合命运,而不是 Notch;numb 双突变体中观察到的 RP2 命运。此外,Neur 的过表达可以诱导两个细胞都采用类似于获得功能 Notch 的 sib 命运。我们的结果通过单个参与者 Neur 将 Numb 和 Notch 信号联系起来,从而使我们对围绕前体细胞不对称分裂的事件有了更完整的了解。我们还表明,Neur 和 Numb 对它们的不对称定位是相互依赖的。