Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/200574
Type: Artigo de periódico
Title: New Mutation In The Myocilin Gene Segregates With Juvenile-onset Open-angle Glaucoma In A Brazilian Family.
Author: Braghini, Carolina Ayumi
Neshich, Izabella Agostinho Pena
Neshich, Goran
Soardi, Fernanda Caroline
de Mello, Maricilda Palandi
Costa, Vital Paulino
de Vasconcellos, José Paulo Cabral
de Melo, Mônica Barbosa
Abstract: Mutations in the myocilin gene (MYOC) account for most cases of autosomal dominant juvenile-onset open-angle glaucoma (JOAG), an earlier and more severe form of POAG. We accessed seven members of a Brazilian JOAG family by clinical and molecular investigation. Four out of seven family members were diagnosed with JOAG. All of these patients presented high intraocular pressure and two of them were bilaterally blind. The disease onset varied from 20 to 30years old. There was a nine-year-old family member who had not yet manifested the disease, although he was also a carrier of the mutation. Ophthalmologic examination included: evaluation of the visual field and optic disc, intraocular pressure measurement, and gonioscopy. The three exons and intron/exon junctions of the MYOC gene were screened for mutations through direct sequencing of PCR-amplified DNA fragments. Mutation screening revealed an in-frame mutation in the third exon of the MYOC gene: an insertion of six nucleotides between the cDNA positions 1187 and 1188 (c.1187_1188insCCCAGA, p.D395_E396insDP). This mutation presented an autosomal dominant pattern of inheritance, segregating with the disease in four family members for three generations, and it was absent in 60 normal controls. We also performed a computational structure modeling of olfactomedin-like domain of myocilin protein and conducted in silico analysis to predict the structural changes in the myocilin protein due to the presence of the mutation. These findings may be important for future diagnosis of other presymptomatic family members, as well as for the increase of the panel of MYOC mutations and their effects on phenotype.
Subject: Adult
Age Of Onset
Aged
Amino Acid Sequence
Brazil
Computational Biology
Cytoskeletal Proteins
Dna Mutational Analysis
Exons
Eye Proteins
Female
Genetic Predisposition To Disease
Genetic Testing
Glaucoma, Open-angle
Glycoproteins
Gonioscopy
Humans
Intraocular Pressure
Male
Middle Aged
Molecular Sequence Data
Mutation
Ophthalmology
Optic Disk
Pedigree
Phenotype
Protein Structure, Tertiary
Visual Fields
Young Adult
Rights: fechado
Identifier DOI: 10.1016/j.gene.2013.02.054
Address: http://www.ncbi.nlm.nih.gov/pubmed/23566828
Date Issue: 2013
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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