Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish

Primary congenital glaucoma (PCG) is a heterogeneous, inherited, and severe optical neuropathy caused by apoptotic degeneration of the retinal ganglion cell layer. Whole-exome sequencing analysis of one PCG family identified two affected siblings who carried a low-frequency homozygous nonsense GUCA1...

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Detalles Bibliográficos
Autores: Morales Cámara, Samuel, Alexandre Moreno, Susana, Bonet Fernández, Juan Manuel, Atienzar Aroca, Raquel, Aroca Aguilar, José Daniel, Ferre Fernández, Jesús José, Méndez Hernández, Carmen Dora, Morales Fernández, Laura, Fernández Sánchez, Laura, Cuenca Navarro, Nicolás, Coca Prados, Miguel, Martínez de la Casa Fernández-Borrella, José María, García Feijoo, Julián, Escribano Martínez, Julio
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universidad de Castilla-La Mancha
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/29134
Acceso en línea:https://hdl.handle.net/10578/29134
Access Level:acceso abierto
Palabra clave:Primary congenital glaucoma
Exome sequencing
GUCA1C
GCAP3
Zebrafish
CRISPR/Cas9
Descripción
Sumario:Primary congenital glaucoma (PCG) is a heterogeneous, inherited, and severe optical neuropathy caused by apoptotic degeneration of the retinal ganglion cell layer. Whole-exome sequencing analysis of one PCG family identified two affected siblings who carried a low-frequency homozygous nonsense GUCA1C variant (c.52G > T/p.Glu18Ter/rs143174402). This gene encodes GCAP3, a member of the guanylate cyclase activating protein family, involved in phototransduction andwith a potential role in intraocularpressure regulation. Segregation analysis supported thenotionthat thevariantwas coinherited with the disease in an autosomal recessive fashion. GCAP3 was detected immunohistochemically in the adult human ocular ciliary epithelium and retina. To evaluate the ocular effect of GUCA1C loss-of-function, a guca1c knockout zebrafish line was generated by CRISPR/Cas9 genome editing. Immunohistochemistry demonstrated the presence of GCAP3 in the non-pigmented ciliary epithelium and retina of adult wild-type fishes. Knockout animals presented up-regulation of the glial fibrillary acidic protein in Müller cells and evidence of retinal ganglion cell apoptosis, indicating the existence of gliosis and glaucoma-like retinal damage. In summary, our data provide evidence for the role of GUCA1C as a candidate gene in PCG and offer new insights into the function of this gene in the ocular anterior segment and the retina.

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