Yang Y, Bauer C, Strasser G, Wollman R, Julien J P, Fuchs E
Howard Hughes Medical Institute, Department of Molecular Genetics and Cell Biology, Chicago, Illinois 60637, USA.
Cell. 1999 Jul 23;98(2):229-38. doi: 10.1016/s0092-8674(00)81017-x.
Sensory neurodegeneration occurs in mice defective in BPAG1, a gene encoding cytoskeletal linker proteins capable of anchoring neuronal intermediate filaments to actin cytoskeleton. While BPAG1 null mice fail to anchor neurofilaments (NFs), BPAG1/NF null mice still degenerate in the absence of NFs. We report a novel neural splice form that lacks the actin-binding domain and instead binds and stabilizes microtubules. This interaction is functionally important; in mice and in vitro, neurons lacking BPAG1 display short, disorganized, and unstable microtubules defective in axonal transport. Ironically, BPAG1 neural isoforms represent microtubule-associated proteins that when absent lead to devastating consequences. Moreover, BPAG1 can functionally account for the extraordinary stability of axonal microtubules necessary for transport over long distances. Its isoforms interconnect all three cytoskeletal networks, a feature apparently central to neuronal survival.
感觉神经退行性变发生在BPAG1缺陷的小鼠中,BPAG1是一种编码细胞骨架连接蛋白的基因,该蛋白能够将神经元中间丝锚定到肌动蛋白细胞骨架上。虽然BPAG1基因敲除小鼠无法锚定神经丝(NFs),但BPAG1/NF基因敲除小鼠在没有NFs的情况下仍会发生退变。我们报告了一种新的神经剪接形式,它缺乏肌动蛋白结合结构域,而是结合并稳定微管。这种相互作用在功能上很重要;在小鼠体内和体外实验中,缺乏BPAG1的神经元表现出短的、无序的和不稳定的微管,轴突运输存在缺陷。具有讽刺意味的是,BPAG1神经异构体代表微管相关蛋白,缺失时会导致毁灭性后果。此外,BPAG1在功能上可以解释长距离运输所需的轴突微管的非凡稳定性。其异构体连接所有三个细胞骨架网络,这一特征显然是神经元存活的关键。