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Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene

Baz-Redón, Noelia; Sánchez-Bellver, Laura; Fernández-Cancio, Mónica; Rovira-Amigo, Sandra; Burgoyne, Thomas; Rai, Ranjit; Aquino, Virginia; Toro-Barrios, Noemí; Carmona, Rosario; Polverino, Eva; Cols, Maria; Moreno-Galdó, Antonio; Camats-Tarruella, Núria; Marfany, Gemma

Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene Thumbnail


Authors

Noelia Baz-Redón

Laura Sánchez-Bellver

Mónica Fernández-Cancio

Sandra Rovira-Amigo

Thomas Burgoyne

Profile image of Ranjit Rai

Ranjit Rai ranjit.k.rai@durham.ac.uk
PGR Student Doctor of Philosophy

Virginia Aquino

Noemí Toro-Barrios

Rosario Carmona

Eva Polverino

Maria Cols

Antonio Moreno-Galdó

Núria Camats-Tarruella

Gemma Marfany



Abstract

We report a novel RPGR missense variant co-segregated with a familial X-linked retinitis pigmentosa (XLRP) case. The brothers were hemizygous for this variant, but only the proband presented with primary ciliary dyskinesia (PCD). Thus, we aimed to elucidate the role of the RPGR variant and other modifier genes in the phenotypic variability observed in the family and its impact on motile cilia. The pathogenicity of the variant on the RPGR protein was evaluated by in vitro studies transiently transfecting the mutated RPGR gene, and immunofluorescence analysis on nasal brushing samples. Whole-exome sequencing was conducted to identify potential modifier variants. In vitro studies showed that the mutated RPGR protein could not localise to the cilium and impaired cilium formation. Accordingly, RPGR was abnormally distributed in the siblings’ nasal brushing samples. In addition, a missense variant in CEP290 was identified. The concurrent RPGR variant influenced ciliary mislocalisation of the protein. We provide a comprehensive characterisation of motile cilia in this XLRP family, with only the proband presenting PCD symptoms. The variant’s pathogenicity was confirmed, although it alone does not explain the respiratory symptoms. Finally, the CEP290 gene may be a potential modifier for respiratory symptoms in patients with RPGR mutations.

Citation

Baz-Redón, N., Sánchez-Bellver, L., Fernández-Cancio, M., Rovira-Amigo, S., Burgoyne, T., Rai, R., Aquino, V., Toro-Barrios, N., Carmona, R., Polverino, E., Cols, M., Moreno-Galdó, A., Camats-Tarruella, N., & Marfany, G. (2024). Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene. Cells, 13(6), Article 524. https://doi.org/10.3390/cells13060524

Journal Article Type Article
Acceptance Date Mar 13, 2024
Online Publication Date Mar 16, 2024
Publication Date Mar 16, 2024
Deposit Date May 22, 2024
Publicly Available Date May 22, 2024
Journal Cells
Electronic ISSN 2073-4409
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 13
Issue 6
Article Number 524
DOI https://doi.org/10.3390/cells13060524
Public URL https://durham-repository.worktribe.com/output/2456007

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