Song Ran, Koo Bon-Kyoung, Yoon Ki-Jun, Yoon Mi-Jeong, Yoo Kyeong-Won, Kim Hyun-Taek, Oh Hyeon-Jeong, Kim Yoon-Young, Han Jin-Kwan, Kim Cheol-Hee, Kong Young-Yun
Division of Molecular and Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk 790-784, South Korea.
J Biol Chem. 2006 Nov 24;281(47):36391-400. doi: 10.1074/jbc.M606601200. Epub 2006 Sep 26.
Mutations in Drosophila neuralized (Dneur) result in a variety of developmental defects that closely resemble those of Notch mutants and other Notch pathway mutants. However, mice with disrupted neur1 do not show any aberrant cell fate specifications in neurogenesis and somitogenesis. Thus, we speculated that other vertebrate neur homolog(s) might compensate for loss of the neur gene. Here, we report the paralog of mouse Neur1, named Neuralized-2 (Neur2), which is a ubiquitin-protein isopeptide ligase (E3) that interacts with and ubiquitinates Delta. Both murine Neur1 and Neur2 have similar degrees of homology to DNeur, and neur2 is expressed in patterns similar to those of neur1 in embryos, suggesting potential functional redundancy. Interestingly, two distinct classes of E3 ligases, Mind bomb-1 (Mib1) and Neur2, have cooperative but distinct roles in Delta endocytosis to Hrs-positive vesicles, i.e. Mib1 functions in the initial step of Delta endocytosis, and Neur2 is required for targeting endocytosed Delta to Hrs-positive vesicles. Thus, our study provides a new insight into how distinct E3 ligases work together in the endocytic pathways for Notch signaling.
果蝇神经化基因(Dneur)的突变会导致多种发育缺陷,这些缺陷与Notch突变体及其他Notch信号通路突变体的缺陷极为相似。然而,神经1基因(neur1)功能缺失的小鼠在神经发生和体节发生过程中并未表现出任何异常的细胞命运特化现象。因此,我们推测其他脊椎动物的神经化基因同源物可能会补偿神经化基因的缺失。在此,我们报道了小鼠神经1基因(Neur1)的旁系同源基因,命名为神经化-2(Neur2),它是一种泛素-蛋白质异肽连接酶(E3),可与Delta相互作用并使其泛素化。小鼠的Neur1和Neur2与Dneur具有相似程度的同源性,且Neur2在胚胎中的表达模式与Neur1相似,这表明它们可能具有潜在的功能冗余性。有趣的是,两类不同的E3连接酶,即Mind bomb-1(Mib1)和Neur2,在Delta向Hrs阳性囊泡的内吞作用中具有协同但不同的作用,也就是说,Mib1在Delta内吞作用的起始步骤中发挥作用,而Neur2则是将内吞的Delta靶向Hrs阳性囊泡所必需的。因此,我们的研究为不同的E3连接酶如何在Notch信号的内吞途径中协同工作提供了新的见解。