Xiang Xin, Qiu Rongde, Yao Xuanli, Arst Herbert N, Peñalva Miguel A, Zhang Jun
Department of Biochemistry and Molecular Biology, F. Edward Hébert School of Medicine, The Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD, 20814, USA,
Cell Mol Life Sci. 2015 Sep;72(17):3267-80. doi: 10.1007/s00018-015-1926-y. Epub 2015 May 23.
Microtubule-based distribution of organelles/vesicles is crucial for the function of many types of eukaryotic cells and the molecular motor cytoplasmic dynein is required for transporting a variety of cellular cargos toward the microtubule minus ends. Early endosomes represent a major cargo of dynein in filamentous fungi, and dynein regulators such as LIS1 and the dynactin complex are both required for early endosome movement. In fungal hyphae, kinesin-3 and dynein drive bi-directional movements of early endosomes. Dynein accumulates at microtubule plus ends; this accumulation depends on kinesin-1 and dynactin, and it is important for early endosome movements towards the microtubule minus ends. The physical interaction between dynein and early endosome requires the dynactin complex, and in particular, its p25 component. The FTS-Hook-FHIP (FHF) complex links dynein-dynactin to early endosomes, and within the FHF complex, Hook interacts with dynein-dynactin, and Hook-early endosome interaction depends on FHIP and FTS.
基于微管的细胞器/囊泡分布对于多种真核细胞的功能至关重要,而分子马达胞质动力蛋白是将多种细胞货物向微管负端运输所必需的。早期内体是丝状真菌中动力蛋白的主要货物,动力蛋白调节因子如LIS1和动力蛋白激活蛋白复合体对于早期内体的移动都是必需的。在真菌菌丝中,驱动蛋白-3和动力蛋白驱动早期内体的双向移动。动力蛋白聚集在微管正端;这种聚集依赖于驱动蛋白-1和动力蛋白激活蛋白,并且对于早期内体向微管负端的移动很重要。动力蛋白与早期内体之间的物理相互作用需要动力蛋白激活蛋白复合体,特别是其p25组分。FTS-Hook-FHIP(FHF)复合体将动力蛋白-动力蛋白激活蛋白与早期内体连接起来,并且在FHF复合体内,Hook与动力蛋白-动力蛋白激活蛋白相互作用,而Hook-早期内体相互作用依赖于FHIP和FTS。