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LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells.
Kawamura, Yuichi; Suga, Akiko; Fujimaki, Takuro; Yoshitake, Kazutoshi; Tsunoda, Kazushige; Murakami, Akira; Iwata, Takeshi.
Afiliação
  • Kawamura Y; Division of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization, Tokyo Medical Center, 2-5-1, Higashigaoka, Meguro-ku, Tokyo, 152-8902, Japan.
  • Suga A; Department of Ophthalmology, Juntendo University Graduate School of Medicine, 2-1-1, Hongou, Bunkyo-ku, Tokyo, 113-8421, Japan.
  • Fujimaki T; Division of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization, Tokyo Medical Center, 2-5-1, Higashigaoka, Meguro-ku, Tokyo, 152-8902, Japan.
  • Yoshitake K; Department of Ophthalmology, Juntendo University Graduate School of Medicine, 2-1-1, Hongou, Bunkyo-ku, Tokyo, 113-8421, Japan.
  • Tsunoda K; Division of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization, Tokyo Medical Center, 2-5-1, Higashigaoka, Meguro-ku, Tokyo, 152-8902, Japan.
  • Murakami A; Division of Vision Research, National Institute of Sensory Organs, National Hospital Organization, Tokyo Medical Center, 2-5-1, Higashigaoka, Meguro-ku, Tokyo, 152-8902, Japan.
  • Iwata T; Department of Ophthalmology, Juntendo University Graduate School of Medicine, 2-1-1, Hongou, Bunkyo-ku, Tokyo, 113-8421, Japan.
J Hum Genet ; 63(8): 893-900, 2018 Aug.
Article em En | MEDLINE | ID: mdl-29760528
The macula is a unique structure in higher primates, where cone and rod photoreceptors show highest density in the fovea and the surrounding area, respectively. The hereditary macular dystrophies represent a heterozygous group of rare disorders characterized by central visual loss and atrophy of the macula and surrounding retina. Here we report an atypical absence of ON-type bipolar cell response in a Japanese patient with autosomal dominant macular dystrophy (adMD). To identify a causal genetic mutation for the adMD, we performed whole-exome sequencing (WES) on four affected and four-non affected members of the family for three generations, and identified a novel p.C538Y mutation in a post-synaptic gene, LRRTM4. WES analysis revealed seven rare genetic variations in patients. We further referred to our in-house WES data from 1360 families with inherited retinal diseases, and found that only p.C538Y mutation in LRRTM4 was associated with adMD-affected patients. Combinatorial filtration using public database of single-nucleotide polymorphism frequency and genotype-phenotype annotated database identified novel mutation in atypical adMD.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Células Bipolares da Retina / Estudos de Associação Genética / Degeneração Macular / Proteínas de Membrana / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Animals / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Células Bipolares da Retina / Estudos de Associação Genética / Degeneração Macular / Proteínas de Membrana / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Animals / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão