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CEP170 在纤毛功能和动力蛋白-2 组装中的作用。

Roles for CEP170 in cilia function and dynein-2 assembly.

机构信息

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.

出版信息

J Cell Sci. 2024 Apr 15;137(8). doi: 10.1242/jcs.261816. Epub 2024 May 1.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a109/11112123/ae4cd6646a23/joces-137-261816-g1.jpg

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