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Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants
Journal article   Open access   Peer reviewed

Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants

Samuel G Jacobson, Artur V Cideciyan, Igor V Peshenko, Alexander Sumaroka, Elena V Olshevskaya, Lihui Cao, Sharon B Schwartz, Alejandro J Roman, Melani B Olivares, Sam Sadigh, …
Human molecular genetics, Vol.22(1), pp.168-183
01/01/2013
DOI: 10.1093/hmg/dds421
PMCID: PMC3606011
PMID: 23035049
url
https://doi.org/10.1093/hmg/dds421View
Published (Version of record) Open Access

Abstract

The GUCY2D gene encodes retinal membrane guanylyl cyclase (RetGC1), a key component of the phototransduction machinery in photoreceptors. Mutations in GUCY2D cause Leber congenital amaurosis type 1 (LCA1), an autosomal recessive human retinal blinding disease. The effects of RetGC1 deficiency on human rod and cone photoreceptor structure and function are currently unknown. To move LCA1 closer to clinical trials, we characterized a cohort of patients (ages 6 months-37 years) with GUCY2D mutations. In vivo analyses of retinal architecture indicated intact rod photoreceptors in all patients but abnormalities in foveal cones. By functional phenotype, there were patients with and those without detectable cone vision. Rod vision could be retained and did not correlate with the extent of cone vision or age. In patients without cone vision, rod vision functioned unsaturated under bright ambient illumination. In vitro analyses of the mutant alleles showed that in addition to the major truncation of the essential catalytic domain in RetGC1, some missense mutations in LCA1 patients result in a severe loss of function by inactivating its catalytic activity and/or ability to interact with the activator proteins, GCAPs. The differences in rod sensitivities among patients were not explained by the biochemical properties of the mutants. However, the RetGC1 mutant alleles with remaining biochemical activity in vitro were associated with retained cone vision in vivo. We postulate a relationship between the level of RetGC1 activity and the degree of cone vision abnormality, and argue for cone function being the efficacy outcome in clinical trials of gene augmentation therapy in LCA1.
 Catalytic Domain Humans Child, Preschool Receptors, Cell Surface - metabolism Guanylate Cyclase - metabolism Infant Male Mutation, Missense Young Adult Leber Congenital Amaurosis - enzymology Adolescent Adult Female Guanylate Cyclase - genetics Photoreceptor Cells, Vertebrate - metabolism Child Leber Congenital Amaurosis - therapy Retinal Cone Photoreceptor Cells - metabolism Cohort Studies Receptors, Cell Surface - genetics

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