A Short Sequence Targets Transmembrane Proteins to Primary Cilia

Author:

Macarelli Viviana12ORCID,Harding Edward C.1ORCID,Gershlick David C.3ORCID,Merkle Florian T.12ORCID

Affiliation:

1. Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, UK

2. Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, UK

3. Cambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, UK

Abstract

Primary cilia are finger-like sensory organelles that extend from the bodies of most cell types and have a distinct lipid and protein composition from the plasma membrane. This partitioning is maintained by a diffusion barrier that restricts the entry of non-ciliary proteins, and allows the selective entry of proteins harboring a ciliary targeting sequence (CTS). However, CTSs are not stereotyped and previously reported sequences are insufficient to drive efficient ciliary localisation across diverse cell types. Here, we describe a short peptide sequence that efficiently targets transmembrane proteins to primary cilia in all tested cell types, including human neurons. We generate human-induced pluripotent stem cell (hiPSC) lines stably expressing a transmembrane construct bearing an extracellular HaloTag and intracellular fluorescent protein, which enables the bright, specific labeling of primary cilia in neurons and other cell types to facilitate studies of cilia in health and disease. We demonstrate the utility of this resource by developing an image analysis pipeline for the automated measurement of primary cilia to detect changes in their length associated with altered signaling or disease state.

Funder

New York Stem Cell Foundation

Ben Barres

Wellcome Trust and Royal Society

Wellcome Trust/Royal Society

Biotechnology and Biological Sciences Research Council

Publisher

MDPI AG

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