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Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy

Progressive retinal degenerations are among the most common causes of blindness both in human and in dogs. Canine progressive retinal atrophy (PRA) resembles human retinitis pigmentosa (RP) and is typically characterized by a progressive loss of rod photoreceptors followed by a loss of cone function...

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Autores principales: Ahonen, Saija J., Arumilli, Meharji, Seppälä, Eija, Hakosalo, Osmo, Kaukonen, Maria K., Komáromy, András M., Lohi, Hannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269413/
https://www.ncbi.nlm.nih.gov/pubmed/25517981
http://dx.doi.org/10.1371/journal.pone.0114552
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author Ahonen, Saija J.
Arumilli, Meharji
Seppälä, Eija
Hakosalo, Osmo
Kaukonen, Maria K.
Komáromy, András M.
Lohi, Hannes
author_facet Ahonen, Saija J.
Arumilli, Meharji
Seppälä, Eija
Hakosalo, Osmo
Kaukonen, Maria K.
Komáromy, András M.
Lohi, Hannes
author_sort Ahonen, Saija J.
collection PubMed
description Progressive retinal degenerations are among the most common causes of blindness both in human and in dogs. Canine progressive retinal atrophy (PRA) resembles human retinitis pigmentosa (RP) and is typically characterized by a progressive loss of rod photoreceptors followed by a loss of cone function. The disease gradually progress from the loss of night and day vision to a complete blindness. We have recently described a unique form of retinopathy characterized by the multifocal gray/brown discoloration and thinning of the retina in the Swedish Vallhund (SV) breed. We aimed to identify the genetic cause by performing a genome wide association analysis in a cohort of 18 affected and 10 healthy control dogs using Illumina's canine 22k SNP array. We mapped the disease to canine chromosome 17 (p = 7.7×10(−5)) and found a 6.1 Mb shared homozygous region in the affected dogs. A combined analysis of the GWAS and replication data with additional 60 dogs confirmed the association (p = 4.3×10(−8), OR = 11.2 for homozygosity). A targeted resequencing of the entire associated region in four cases and four controls with opposite risk haplotypes identified several variants in the coding region of functional candidate genes, such as a known retinopathy gene, MERTK. However, none of the identified coding variants followed a compelling case- or breed-specific segregation pattern. The expression analyses of four candidate genes in the region, MERTK, NPHP1, ANAPC1 and KRCC1, revealed specific upregulation of MERTK in the retina of the affected dogs. Collectively, these results indicate that the retinopathy is associated with overexpression of MERTK, however further investigation is needed to discover the regulatory mutation for the better understanding of the disease pathogenesis. Our study establishes a novel gain-of-function model for the MERTK biology and provides a therapy model for retinopathy MERTK inhibitors. Meanwhile, a marker-based genetic counseling can be developed to revise breeding programs.
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spelling pubmed-42694132014-12-26 Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy Ahonen, Saija J. Arumilli, Meharji Seppälä, Eija Hakosalo, Osmo Kaukonen, Maria K. Komáromy, András M. Lohi, Hannes PLoS One Research Article Progressive retinal degenerations are among the most common causes of blindness both in human and in dogs. Canine progressive retinal atrophy (PRA) resembles human retinitis pigmentosa (RP) and is typically characterized by a progressive loss of rod photoreceptors followed by a loss of cone function. The disease gradually progress from the loss of night and day vision to a complete blindness. We have recently described a unique form of retinopathy characterized by the multifocal gray/brown discoloration and thinning of the retina in the Swedish Vallhund (SV) breed. We aimed to identify the genetic cause by performing a genome wide association analysis in a cohort of 18 affected and 10 healthy control dogs using Illumina's canine 22k SNP array. We mapped the disease to canine chromosome 17 (p = 7.7×10(−5)) and found a 6.1 Mb shared homozygous region in the affected dogs. A combined analysis of the GWAS and replication data with additional 60 dogs confirmed the association (p = 4.3×10(−8), OR = 11.2 for homozygosity). A targeted resequencing of the entire associated region in four cases and four controls with opposite risk haplotypes identified several variants in the coding region of functional candidate genes, such as a known retinopathy gene, MERTK. However, none of the identified coding variants followed a compelling case- or breed-specific segregation pattern. The expression analyses of four candidate genes in the region, MERTK, NPHP1, ANAPC1 and KRCC1, revealed specific upregulation of MERTK in the retina of the affected dogs. Collectively, these results indicate that the retinopathy is associated with overexpression of MERTK, however further investigation is needed to discover the regulatory mutation for the better understanding of the disease pathogenesis. Our study establishes a novel gain-of-function model for the MERTK biology and provides a therapy model for retinopathy MERTK inhibitors. Meanwhile, a marker-based genetic counseling can be developed to revise breeding programs. Public Library of Science 2014-12-17 /pmc/articles/PMC4269413/ /pubmed/25517981 http://dx.doi.org/10.1371/journal.pone.0114552 Text en © 2014 Ahonen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ahonen, Saija J.
Arumilli, Meharji
Seppälä, Eija
Hakosalo, Osmo
Kaukonen, Maria K.
Komáromy, András M.
Lohi, Hannes
Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
title Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
title_full Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
title_fullStr Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
title_full_unstemmed Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
title_short Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy
title_sort increased expression of mertk is associated with a unique form of canine retinopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269413/
https://www.ncbi.nlm.nih.gov/pubmed/25517981
http://dx.doi.org/10.1371/journal.pone.0114552
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