Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK.
School of Molecular and Cellular Biology, University of Leeds, Leeds, UK.
Hum Mutat. 2021 Feb;42(2):164-176. doi: 10.1002/humu.24140. Epub 2020 Nov 30.
Biallelic mutations in G-Protein coupled receptor kinase 1 (GRK1) cause Oguchi disease, a rare subtype of congenital stationary night blindness (CSNB). The purpose of this study was to identify disease causing GRK1 variants and use in-depth bioinformatic analyses to evaluate how their impact on protein structure could lead to pathogenicity. Patients' genomic DNA was sequenced by whole genome, whole exome or focused exome sequencing. Disease associated variants, published and novel, were compared to nondisease associated missense variants. The impact of GRK1 missense variants at the protein level were then predicted using a series of computational tools. We identified twelve previously unpublished cases with biallelic disease associated GRK1 variants, including eight novel variants, and reviewed all GRK1 disease associated variants. Further structure-based scoring revealed a hotspot for missense variants in the kinase domain. In addition, to aid future clinical interpretation, we identified the bioinformatics tools best able to differentiate disease associated from nondisease associated variants. We identified GRK1 variants in Oguchi disease patients and investigated how disease-causing variants may impede protein function in-silico.
G 蛋白偶联受体激酶 1(GRK1)的双等位基因突变导致奥古斯特病,这是先天性静止性夜盲症(CSNB)的一种罕见亚型。本研究旨在鉴定致病的 GRK1 变体,并利用深入的生物信息学分析来评估其对蛋白质结构的影响如何导致致病性。通过全基因组、全外显子或靶向外显子测序对患者的基因组 DNA 进行测序。将新发现的和已发表的与疾病相关的变异与非疾病相关的错义变异进行比较。然后使用一系列计算工具预测 GRK1 错义变异在蛋白质水平上的影响。我们确定了 12 个以前未发表的具有双等位基因疾病相关 GRK1 变体的病例,包括 8 个新变体,并回顾了所有与 GRK1 疾病相关的变体。进一步的基于结构的评分显示激酶结构域中存在错义变异的热点。此外,为了帮助未来的临床解释,我们确定了最能区分疾病相关和非疾病相关变体的生物信息学工具。我们在奥古斯特病患者中鉴定出 GRK1 变体,并研究了致病变体如何在计算机上阻碍蛋白质功能。