Mukherjee Ashim, Veraksa Alexey, Bauer Andreas, Rosse Carine, Camonis Jacques, Artavanis-Tsakonas Spyros
Department of Cell Biology, Harvard Medical School, Massachusetts General Hospital Cancer Center, Charlestown, MA 02129, USA.
Nat Cell Biol. 2005 Dec;7(12):1191-201. doi: 10.1038/ncb1327. Epub 2005 Nov 13.
Signalling activity of the Notch receptor, which plays a fundamental role in metazoan cell fate determination, is controlled at multiple levels. We uncovered a Notch signal-controlling mechanism that depends on the ability of the non-visual beta-arrestin, Kurtz (Krz), to influence the degradation and, consequently, the function of the Notch receptor. We identified Krz as a binding partner of a known Notch-pathway modulator, Deltex (Dx), and demonstrated the existence of a trimeric Notch-Dx-Krz protein complex. This complex mediates the degradation of the Notch receptor through a ubiquitination-dependent pathway. Our results establish a novel mode of regulation of Notch signalling and define a new function for non-visual beta-arrestins.
Notch受体的信号传导活性在多细胞生物细胞命运决定中起基本作用,其在多个水平受到调控。我们发现了一种Notch信号控制机制,该机制依赖于非视觉β-抑制蛋白Kurtz(Krz)影响Notch受体降解从而影响其功能的能力。我们鉴定出Krz是已知的Notch信号通路调节因子Deltex(Dx)的结合伴侣,并证明存在三聚体Notch-Dx-Krz蛋白复合物。该复合物通过泛素化依赖性途径介导Notch受体的降解。我们的结果建立了一种Notch信号调节的新模式,并定义了非视觉β-抑制蛋白的新功能。