Functional analyses of Pericentrin and Syne-2/Nesprin-2 interaction in ciliogenesis

Author:

Falk Nathalie1ORCID,Kessler Kristin1,Schramm Sinja-Fee1ORCID,Boldt Karsten2ORCID,Becirovic Elvir3ORCID,Michalakis Stylianos3ORCID,Regus-Leidig Hanna1ORCID,Noegel Angelika A.4ORCID,Ueffing Marius2ORCID,Thiel Christian T.5ORCID,Roepman Ronald6ORCID,Brandstätter Johann Helmut1,Gießl Andreas1

Affiliation:

1. Animal Physiology, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany

2. Division of Experimental Ophthalmology and Medical Proteome Center, Center of Ophthalmology, University of Tübingen, 72074 Tübingen, Germany

3. Department of Pharmacy – Center for Drug Research, Ludwig-Maximilians-Universität München, Munich, Germany

4. Institute of Biochemistry I; Medical Faculty, University Hospital, University of Cologne; Köln, Germany

5. Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany

6. Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6525 GA, The Netherlands

Abstract

Pericentrin (Pcnt) is a multifunctional scaffold protein and mutations in the human PCNT gene are associated with diseases including ciliopathies. Pcnt plays a crucial role in ciliary development in olfactory receptor neurons, but its function in the photoreceptor connecting cilium is unknown. We downregulated Pcnt in the retina ex vivo and in vivo via a virus-based RNA interference approach to study Pcnt function in photoreceptors. ShRNA-mediated knockdown of Pcnt impaired the development of the photoreceptor connecting cilium and outer segment and showed a nuclear migration defect. In protein interaction screens, we found Syne-2 as an interaction partner of Pcnt in photoreceptors. Syne-2, an outer nuclear membrane protein, is important for positioning murine photoreceptor cell nuclei and for centrosomal migration during early ciliogenesis. CRISPR/Cas9 mediated knockout of Syne-2 in cell culture led to an overexpression and mislocalization of Pcnt and to ciliogenesis defects. Our findings suggest that the Pcnt/Syne-2 complex is important for ciliogenesis and outer segment formation during retinal development and plays a role in nuclear migration.

Funder

Deutsche Forschungsgemeinschaft

Publisher

The Company of Biologists

Subject

Cell Biology

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