Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis

Autor(es)

Motta, Fabiana Louise ^[1] ; Filippelli-Silva, Rafael ^[2] ; Kitajima, Joao Paulo ^[3] ; Batista, Denise A. ^[4] ; Wohler, Elizabeth S. ^[5] ; Sobreira, Nara L. ^[5] ; Martin, Renan Paulo ^{[2, 5]} ; Ferraz Sallum, Juliana Maria ^{[1, 6]}

Afiliação do(s) autor(es)

^[1] Univ Fed Sao Paulo, Dept Ophthalmol, Sao Paulo - Brazil

^[2] Univ Fed Sao Paulo, Dept Biophys, Sao Paulo - Brazil

^[3] Mendel Analise Genom SA, Sao Paulo - Brazil

^[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD - USA

^[5] Johns Hopkins Med, McKusick Nathans Dept Genet Med, Baltimore, MD - USA

^[6] Inst Genet Ocular, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: OPHTHALMIC GENETICS; v. 42, n. 5, p. 553-560, SEP 3 2021.
• Citações Web of Science: 0

Resumo

Purpose: This study aims to demonstrate the possibility of detecting segmental uniparental isodisomy (iUPD) using a next-generation sequencing gene panel by reporting a Leber congenital amaurosis (LCA) case caused by a homozygous pathogenic variant in RPE65 (c.1022 T > C:p.Leu341Ser) inherited exclusively from the proband's mother. Methods: Samples from the trio (proband, mother, and father) were sequenced with a next-generation sequencing (NGS) retinopathy gene panel (224 genes) and the VCF file containing all variants was used in order to determine single nucleotide variant (SNV) counts from each sample across all chromosomes. Results: Trio analysis showed that of 81 Chr1 inherited variants 41 were exclusively maternal, including 21 homozygous. The other 40 variants were common to both parents. On remaining autosomal chromosomes (Chr2-22) 645 inherited variants were found, 147 of them were exclusively maternal and 132 exclusively paternal. Based on these NGS data, it was possible to note that the proband's chromosomes 1 are more similar to his mother's chromosome 1 than his father's, suggesting the pathogenic homozygous variant found in this patient was inherited exclusively from the mother due to uniparental maternal isodisomy. Conclusions: This study presents a secondary analysis pipeline to identify responsible variants for a phenotype and the correct inheritance pattern, which is a critical step to the proper and accurate genetic counseling of all family members. In addition, this approach could be used to determine iUPD in different Mendelian disorders if the sequencing panel identifies variants spread throughout the genome. (AU)

• Processo FAPESP: 14/20965-3 - Estudo in silico de mutações gênicas causadoras do angioedema hereditário
• Beneficiário: Renan Paulo Martin
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado