Roles for CEP170 in cilia function and dynein-2 assembly

Author:

Weijman Johannes F.1ORCID,Vuolo Laura1ORCID,Shak Caroline1ORCID,Pugnetti Anna1,Mukhopadhyay Aakash G.2ORCID,Hodgson Lorna R.3ORCID,Heesom Kate J.4ORCID,Roberts Anthony J.2ORCID,Stephens David J.1ORCID

Affiliation:

1. Cell Biology Laboratories, School of Biochemistry, Faculty of Life Sciences, University of Bristol 1 , Bristol BS8 1TD , UK

2. University of Oxford 2 Sir William Dunn School of Pathology , , Oxford OX1 3RE , UK

3. University Walk, University of Bristol 3 Wolfson Bioimaging Facility, Faculty of Life Sciences , , Bristol BS8 1TD , UK

4. University of Bristol 4 Proteomics Facility, Faculty of Life Sciences , , Bristol BS8 1TD , UK

Abstract

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.

Funder

Biotechnology and Biological Sciences Research Council

Wellcome Trust

University of Bristol

Publisher

The Company of Biologists

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