Cell Biology Laboratories, School of Biochemistry, Faculty of Life Sciences, University of Bristol, Bristol BS8 1TD, UK.
Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
J Cell Sci. 2024 Apr 15;137(8). doi: 10.1242/jcs.261816. Epub 2024 May 1.
Primary cilia are essential eukaryotic organelles required for signalling and secretion. Dynein-2 is a microtubule-motor protein complex and is required for ciliogenesis via its role in facilitating retrograde intraflagellar transport (IFT) from the cilia tip to the cell body. Dynein-2 must be assembled and loaded onto IFT trains for entry into cilia for this process to occur, but how dynein-2 is assembled and how it is recycled back into a cilium remain poorly understood. Here, we identify centrosomal protein of 170 kDa (CEP170) as a dynein-2-interacting protein in mammalian cells. We show that loss of CEP170 perturbs intraflagellar transport and hedgehog signalling, and alters the stability of dynein-2 holoenzyme complex. Together, our data indicate a role for CEP170 in supporting cilia function and dynein-2 assembly.
原发性纤毛是真核生物必需的细胞器,对于信号转导和分泌至关重要。动力蛋白-2 是一种微管动力蛋白复合物,通过在促进逆行纤毛内运输(IFT)从纤毛尖端到细胞体中的作用,对于纤毛发生是必需的。为了使该过程发生,动力蛋白-2 必须组装并加载到 IFT 列车上以进入纤毛,但动力蛋白-2 如何组装以及如何将其回收回纤毛仍然知之甚少。在这里,我们鉴定出中心体蛋白 170kDa(CEP170)是哺乳动物细胞中与动力蛋白-2 相互作用的蛋白。我们表明,CEP170 的缺失会扰乱纤毛内运输和 Hedgehog 信号转导,并改变动力蛋白-2 全酶复合物的稳定性。总之,我们的数据表明 CEP170 在支持纤毛功能和动力蛋白-2 组装方面发挥作用。