Noelia Baz-Redón
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
Authors
Laura Sánchez-Bellver
Mónica Fernández-Cancio
Sandra Rovira-Amigo
Thomas Burgoyne
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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