BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone

Author:

Ye Fan12,Nager Andrew R.2,Nachury Maxence V.12ORCID

Affiliation:

1. Department of Ophthalmology, University of California, San Francisco, San Francisco, CA

2. Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA

Abstract

A diffusion barrier at the transition zone enables the compartmentalization of signaling molecules by cilia. The BBSome and the small guanosine triphosphatase Arl6, which triggers BBSome coat polymerization, are required for the exit of activated signaling receptors from cilia, but how diffusion barriers are crossed when membrane proteins exit cilia remains to be determined. In this study, we found that activation of the ciliary G protein–coupled receptors (GPCRs) Smoothened and SSTR3 drove the Arl6-dependent assembly of large, highly processive, and cargo-laden retrograde BBSome trains. Single-molecule imaging revealed that the assembly of BBSome trains enables the lateral transport of ciliary GPCRs across the transition zone. However, the removal of activated GPCRs from cilia was inefficient because a second periciliary diffusion barrier was infrequently crossed. We conclude that exit from cilia is a two-step process in which BBSome/Arl6 trains first move activated GPCRs through the transition zone before a periciliary barrier can be crossed.

Funder

National Institutes of Health

Damon Runyan Cancer Research Foundation

Publisher

Rockefeller University Press

Subject

Cell Biology

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