The interplay between RPGR, PDEδ and Arl2/3 regulate the ciliary targeting of farnesylated cargo

Wätzlich, D., Vetter, I., Gotthardt, K., Miertzschke, M., Chen, Y.-X., Wittinghofer, A. and Ismail, S. (2013) The interplay between RPGR, PDEδ and Arl2/3 regulate the ciliary targeting of farnesylated cargo. EMBO Reports, 14(5), pp. 465-472. (doi: 10.1038/embor.2013.37) (PMID:23559067) (PMCID:PMC3642377)

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Abstract

Defects in primary cilia result in human diseases known as ciliopathies. The retinitis pigmentosa GTPase regulator (RPGR), mutated in the most severe form of the eye disease, is located at the transition zone of the ciliary organelle. The RPGR-interacting partner PDEδ is involved in trafficking of farnesylated ciliary cargo, but the significance of this interaction is unknown. The crystal structure of the propeller domain of RPGR shows the location of patient mutations and how they perturb the structure. The RPGR·PDEδ complex structure shows PDEδ on a highly conserved surface patch of RPGR. Biochemical experiments and structural considerations show that RPGR can bind with high affinity to cargo-loaded PDEδ and exposes the Arl2/Arl3-binding site on PDEδ. On the basis of these results, we propose a model where RPGR is acting as a scaffold protein recruiting cargo-loaded PDEδ and Arl3 to release lipidated cargo into cilia.

Item Type:Articles
Additional Information:This work was supported by a grant from the European Research Council (ERC grant 268782 to A.W.).
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Ismail, Dr Shehab
Authors: Wätzlich, D., Vetter, I., Gotthardt, K., Miertzschke, M., Chen, Y.-X., Wittinghofer, A., and Ismail, S.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:EMBO Reports
Publisher:EMBO Press
ISSN:1469-221X
ISSN (Online):1469-3178

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