Saito N, Okada Y, Noda Y, Kinoshita Y, Kondo S, Hirokawa N
Department of Anatomy and Cell Biology, Faculty of Medicine, University of Tokyo, Hongo, Japan.
Neuron. 1997 Mar;18(3):425-38. doi: 10.1016/s0896-6273(00)81243-x.
We have cloned two novel C-terminal motor domain-type kinesin superfamily motor proteins (KIFCs) from mouse brain by utilizing a KIFC-specific consensus sequence. The first protein was the murine homologue of CHO2 antigen, a member of the kar3-type mitotic motor subfamily, and we designated this protein KIFC1. The other protein, KIFC2 (792 amino acids), is novel, with no significant similarity to known kinesin superfamily proteins (KIFs). KIFC2 was specifically expressed in adult neurons, and was immunofluorescently localized to punctate structures in cell bodies and dendrites, but was not detected in axons. Electron microscopic analysis of the immunoisolated KIFC2-bound organelles revealed that KIFC2 associates with multivesicular body (mvb)-like organelles, suggesting that KIFC2 functions as the motor for the transport of mvb-like organelles in dendrites.
我们利用KIFC特异性共有序列从小鼠大脑中克隆了两种新型的C末端运动结构域型驱动蛋白超家族运动蛋白(KIFC)。第一种蛋白是CHO2抗原的小鼠同源物,属于kar3型有丝分裂运动亚家族的成员,我们将该蛋白命名为KIFC1。另一种蛋白KIFC2(792个氨基酸)是新型的,与已知的驱动蛋白超家族蛋白(KIF)没有明显的相似性。KIFC2在成年神经元中特异性表达,免疫荧光定位在细胞体和树突中的点状结构上,但在轴突中未检测到。对免疫分离的与KIFC2结合的细胞器进行电子显微镜分析表明,KIFC2与多囊泡体(mvb)样细胞器相关联,这表明KIFC2作为树突中mvb样细胞器运输的动力蛋白发挥作用。