Niwa Shinsuke, Tanaka Yosuke, Hirokawa Nobutaka
Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Nat Cell Biol. 2008 Nov;10(11):1269-79. doi: 10.1038/ncb1785. Epub 2008 Oct 12.
Synaptic proteins are synthesized in the cell body and transported down the axon by microtubule-dependent motors. We previously reported that KIF1Bbeta and KIF1A motors are essential for transporting synaptic vesicle precursors; however the mechanisms that regulate transport, as well as cargo recognition and control of cargo loading and unloading remain largely unknown. Here, we show that DENN/MADD (Rab3-GEP) is an essential part of the regulation mechanism through direct interaction with the stalk domain of KIF1Bbeta and KIF1A. We also show that DENN/MADD binds preferentially to GTP-Rab3 and acts as a Rab3 effector. These molecular interactions are fundamental as sequential genetic perturbations revealed that KIF1Bbeta and KIF1A are essential for the transport of DENN/MADD and Rab3, whereas DENN/MADD is essential for the transport of Rab3. GTP-Rab3 was more effectively transported than GDP-Rab3, suggesting that the nucleotide state of Rab3 regulates axonal transport of Rab3-carrying vesicles through preferential interaction with DENN/MADD.
突触蛋白在细胞体中合成,并由微管依赖的马达沿着轴突运输。我们之前报道过,KIF1Bβ和KIF1A马达对于运输突触小泡前体至关重要;然而,调节运输的机制以及货物识别和货物装卸控制在很大程度上仍然未知。在这里,我们表明DENN/MADD(Rab3鸟嘌呤核苷酸交换因子)通过与KIF1Bβ和KIF1A的柄结构域直接相互作用,是调节机制的重要组成部分。我们还表明,DENN/MADD优先结合GTP-Rab3并作为Rab3效应器发挥作用。这些分子相互作用至关重要,因为连续的基因扰动表明,KIF1Bβ和KIF1A对于DENN/MADD和Rab3的运输至关重要,而DENN/MADD对于Rab3的运输至关重要。GTP-Rab3比GDP-Rab3运输更有效,这表明Rab3的核苷酸状态通过与DENN/MADD的优先相互作用调节携带Rab3的囊泡的轴突运输。