Program in Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.
Development. 2009 Dec;136(24):4089-98. doi: 10.1242/dev.040386. Epub 2009 Nov 11.
Asymmetric cell divisions generate sibling cells of distinct fates ('A', 'B') and constitute a fundamental mechanism that creates cell-type diversity in multicellular organisms. Antagonistic interactions between the Notch pathway and the intrinsic cell-fate determinant Numb appear to regulate asymmetric divisions in flies and vertebrates. During these divisions, productive Notch signaling requires sanpodo, which encodes a novel transmembrane protein. Here, we demonstrate that Drosophila sanpodo plays a dual role to regulate Notch signaling during asymmetric divisions - amplifying Notch signaling in the absence of Numb in the 'A' daughter cell and inhibiting Notch signaling in the presence of Numb in the 'B' daughter cell. In so doing, sanpodo ensures the asymmetry in Notch signaling levels necessary for the acquisition of distinct fates by the two daughter cells. These findings answer long-standing questions about the restricted ability of Numb and Sanpodo to inhibit and to promote, respectively, Notch signaling during asymmetric divisions.
不对称细胞分裂产生具有不同命运的“子细胞 A”和“子细胞 B”,是多细胞生物产生细胞多样性的基本机制。 Notch 通路和内在细胞命运决定因子 Numb 之间的拮抗相互作用似乎调节了果蝇和脊椎动物的不对称细胞分裂。在这些分裂中,有活性的 Notch 信号需要 sanpodo,它编码一种新型的跨膜蛋白。在这里,我们证明果蝇的 sanpodo 在不对称细胞分裂过程中发挥双重作用来调节 Notch 信号:在“子细胞 A”中不存在 Numb 的情况下,增强 Notch 信号;而在“子细胞 B”中存在 Numb 的情况下,抑制 Notch 信号。这样,sanpodo 确保了两个子细胞获得不同命运所需的 Notch 信号水平的不对称性。这些发现回答了关于 Numb 和 Sanpodo 在不对称细胞分裂中分别抑制和促进 Notch 信号的有限能力的长期存在的问题。