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一个家族中存在 Eyes Shut Homolog(EYS)基因突变导致的假性显性遗传的视网膜色素变性。

Pseudodominant inheritance of retinitis pigmentosa in a family with mutations in the Eyes Shut Homolog (EYS) gene.

机构信息

Department of Molecular Medicine, University of Padova, 35121, Padova, Italy.

Clinical Genetics Unit, Azienda Ospedaliero Universitaria di Padova, 35121, Padova, Italy.

出版信息

Sci Rep. 2024 Aug 10;14(1):18580. doi: 10.1038/s41598-024-69640-9.

Abstract

Sequence variants in Eyes Shut Homolog (EYS) gene are one of the most frequent causes of autosomal recessive retinitis pigmentosa (RP). Herein, we describe an Italian RP family characterized by EYS-related pseudodominant inheritance. The female proband, her brother, and both her sons showed typical RP, with diminished or non-recordable full-field electroretinogram, narrowing of visual field, and variable losses of central vision. To investigate this apparently autosomal dominant pedigree, next generation sequencing (NGS) of a custom panel of RP-related genes was performed, further enhanced by bioinformatic detection of copy-number variations (CNVs). Unexpectedly, all patients had a compound heterozygosity involving two known pathogenic EYS variants i.e., the exon 33 frameshift mutation c.6714delT and the exon 29 deletion c.(5927þ1_5928-1)_(6078þ1_6079-1)del, with the exception of the youngest son who was homozygous for the above-detailed frameshift mutation. No pathologic eye conditions were instead observed in the proband's husband, who was a heterozygous healthy carrier of the same c.6714delT variant in exon 33 of EYS gene. These findings provide evidence that pseudodominant pattern of inheritance can hide an autosomal recessive RP partially or totally due to CNVs, recommending CNVs study in those pedigrees which remain genetically unsolved after the completion of NGS or whole exome sequencing analysis.

摘要

Eyes Shut Homolog (EYS) 基因中的序列变异是常染色体隐性遗传视网膜色素变性 (RP) 的最常见原因之一。在此,我们描述了一个意大利 RP 家族,其特征为 EYS 相关的拟显性遗传。女性先证者、她的兄弟和两个儿子均表现出典型的 RP,全视野视网膜电图减弱或无法记录,视野变窄,中心视力可变丧失。为了研究这个明显的常染色体显性遗传家系,对 RP 相关基因的定制面板进行了下一代测序 (NGS),并通过生物信息学检测拷贝数变异 (CNVs) 进一步增强。出乎意料的是,所有患者均为涉及两个已知致病性 EYS 变异的复合杂合性,即外显子 33 移码突变 c.6714delT 和外显子 29 缺失 c.(5927þ1_5928-1)_(6078þ1_6079-1)del,除了最年轻的儿子为上述详细移码突变的纯合子。然而,先证者的丈夫未观察到病理性眼部疾病,他是 EYS 基因外显子 33 中相同 c.6714delT 变异的杂合健康携带者。这些发现表明,拟显性遗传模式可能由于 CNVs 而部分或完全掩盖常染色体隐性 RP,建议对 NGS 或全外显子测序分析完成后仍未遗传解决的家系进行 CNVs 研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/11316741/2d74684b43b9/41598_2024_69640_Fig1_HTML.jpg

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