National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore, India.
PLoS Genet. 2010 Nov 4;6(11):e1001200. doi: 10.1371/journal.pgen.1001200.
UNC-104/KIF1A is a Kinesin-3 motor that transports synaptic vesicles from the cell body towards the synapse by binding to PI(4,5)P(2) through its PH domain. The fate of the motor upon reaching the synapse is not known. We found that wild-type UNC-104 is degraded at synaptic regions through the ubiquitin pathway and is not retrogradely transported back to the cell body. As a possible means to regulate the motor, we tested the effect of cargo binding on UNC-104 levels. The unc-104(e1265) allele carries a point mutation (D1497N) in the PI(4,5)P(2) binding pocket of the PH domain, resulting in greatly reduced preferential binding to PI(4,5)P(2)in vitro and presence of very few motors on pre-synaptic vesicles in vivo. unc-104(e1265) animals have poor locomotion irrespective of in vivo PI(4,5)P(2) levels due to reduced anterograde transport. Moreover, they show highly reduced levels of UNC-104 in vivo. To confirm that loss of cargo binding specificity reduces motor levels, we isolated two intragenic suppressors with compensatory mutations within the PH domain. These show partial restoration of in vitro preferential PI(4,5)P(2) binding and presence of more motors on pre-synaptic vesicles in vivo. These animals show improved locomotion dependent on in vivo PI(4,5)P(2) levels, increased anterograde transport, and partial restoration of UNC-104 protein levels in vivo. For further proof, we mutated a conserved residue in one suppressor background. The PH domain in this triple mutant lacked in vitro PI(4,5)P(2) binding specificity, and the animals again showed locomotory defects and reduced motor levels. All allelic variants show increased UNC-104 levels upon blocking the ubiquitin pathway. These data show that inability to bind cargo can target motors for degradation. In view of the observed degradation of the motor in synaptic regions, this further suggests that UNC-104 may get degraded at synapses upon release of cargo.
UNC-104/KIF1A 是一种驱动蛋白-3,通过其 PH 结构域与 PI(4,5)P(2)结合,将突触囊泡从细胞体运输到突触。驱动蛋白到达突触后的命运尚不清楚。我们发现野生型 UNC-104 通过泛素途径在突触区域降解,并且不会逆行回细胞体。作为一种可能的调节机制,我们测试了货物结合对 UNC-104 水平的影响。unc-104(e1265)等位基因在 PH 结构域的 PI(4,5)P(2)结合口袋中携带一个点突变(D1497N),导致 UNC-104 在体外对 PI(4,5)P(2)的优先结合大大降低,体内突触前囊泡上的驱动蛋白数量也很少。由于正向运输减少,unc-104(e1265)动物无论体内 PI(4,5)P(2)水平如何,运动能力都很差。此外,它们在体内 UNC-104 的水平也显著降低。为了证实丧失货物结合特异性会降低驱动蛋白的水平,我们在 PH 结构域内分离了两个具有补偿突变的基因内抑制子。这些抑制子在体外优先结合 PI(4,5)P(2)和体内突触前囊泡上存在更多驱动蛋白的能力得到部分恢复。这些动物的运动能力取决于体内 PI(4,5)P(2)水平,正向运输增加,体内 UNC-104 蛋白水平部分恢复。为了进一步证明,我们在一个抑制子背景中突变了一个保守残基。这个三突变体的 PH 结构域缺乏体外 PI(4,5)P(2)结合特异性,动物再次表现出运动缺陷和驱动蛋白水平降低。所有等位基因变体在阻断泛素途径后 UNC-104 水平升高。这些数据表明,不能结合货物可以将驱动蛋白靶向降解。鉴于观察到驱动蛋白在突触区域降解,这进一步表明 UNC-104 可能在释放货物后在突触处降解。