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在 Hailey-Hailey 病患者中鉴定出 ATP2C1 的新型和反复出现的变体。

Novel and recurrent variants of ATP2C1 identified in patients with Hailey-Hailey disease.

机构信息

Medical Genetics Department, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, PL, Poland.

Department of Dermatology and Immunodermatology, Medical University of Warsaw, Koszykowa 82A, 00-001, Warsaw, PL, Poland.

出版信息

J Appl Genet. 2020 May;61(2):187-193. doi: 10.1007/s13353-020-00538-8. Epub 2020 Jan 25.

Abstract

Hailey-Hailey disease (HHD) is a rare, late-onset autosomal dominant genodermatosis characterized by blisters, vesicular lesions, crusted erosions, and erythematous scaly plaques predominantly in intertriginous regions. HHD is caused by ATP2C1 mutations. About 180 distinct mutations have been identified so far; however, data of only few cases from Central Europe are available. The aim was to analyze the ATP2C1 gene in a cohort of Polish HHD patients. A group of 18 patients was enrolled in the study based on specific clinical symptoms. Mutations were detected using Sanger or next generation sequencing. In silico analysis was performed by prediction algorisms and dynamic structural modeling. In two cases, mRNA analysis was performed to confirm aberrant splicing. We detected 13 different mutations, including 8 novel, 2 recurrent (p.Gly850Ter and c.325-3 T > G), and 6 sporadic (c.423-1G > T, c.899 + 1G > A, p.Leu539Pro, p.Thr808TyrfsTer16, p.Gln855Arg and a complex allele: c.[1610C > G;1741 + 3A > G]). In silico analysis shows that all novel missense variants are pathogenic or likely pathogenic. We confirmed pathogenic status for two novel variants c.325-3 T > G and c.[1610C > G;1741 + 3A > G] by mRNA analysis. Our results broaden the knowledge about genetic heterogeneity in Central European patients with ATP2C1 mutations and also give further evidence that careful and multifactorial evaluation of variant pathogenicity status is essential.

摘要

Hailey-Hailey 病(HHD)是一种罕见的迟发性常染色体显性遗传皮肤病,其特征为水疱、疱疹样病变、结痂性糜烂和红斑性鳞屑性斑块,主要发生于皱褶部位。HHD 由 ATP2C1 基因突变引起。迄今为止,已经鉴定出大约 180 种不同的突变;然而,来自中欧的数据仅适用于少数病例。本研究旨在分析一组波兰 HHD 患者的 ATP2C1 基因。根据特定的临床症状,招募了 18 名患者参加研究。使用 Sanger 或下一代测序检测突变。通过预测算法和动态结构建模进行了体外分析。在两种情况下,进行了 mRNA 分析以确认异常剪接。我们检测到 13 种不同的突变,包括 8 种新突变、2 种重复突变(p.Gly850Ter 和 c.325-3 T > G)和 6 种散发性突变(c.423-1 G > T、c.899 + 1 G > A、p.Leu539Pro、p.Thr808TyrfsTer16、p.Gln855Arg 和一个复杂等位基因:c.[1610C > G;1741 + 3A > G])。体外分析表明,所有新的错义突变都是致病性或可能致病性的。我们通过 mRNA 分析证实了两个新的突变 c.325-3 T > G 和 c.[1610C > G;1741 + 3A > G]的致病性。我们的结果拓宽了对中欧 ATP2C1 突变患者遗传异质性的认识,并进一步证明了仔细和多因素评估变异致病性状态至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d108/7148260/c829b1a5f3bb/13353_2020_538_Fig1_HTML.jpg

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