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应用定制的 NGS 基因 panel 为遗传性共济失调的分子检测提供了高诊断效用。

Application of a custom NGS gene panel revealed a high diagnostic utility for molecular testing of hereditary ataxias.

机构信息

Department of Genetics, Institute of Psychiatry and Neurology, 9 Sobieskiego Street, 02-957, Warsaw, Poland.

Department of Internal Medicine and Gerontology, Faculty of Medicine, Jagiellonian University Medical College, Krakow, Poland.

出版信息

J Appl Genet. 2022 Sep;63(3):513-525. doi: 10.1007/s13353-022-00701-3. Epub 2022 May 19.

DOI:10.1007/s13353-022-00701-3
PMID:35588347
Abstract

Hereditary ataxias (HA) are a rare group of heterogeneous disorders. Here, we present the results of molecular testing of a group of ataxia patients using a custom-designed next-generation sequencing (NGS) panel. Due to the genetic and clinical overlapping of hereditary ataxias and spastic paraplegias (HSP), the panel encompasses together HA and HSP genes. The NGS libraries, comprising coding sequences for 152 genes, were performed using KAPA HyperPlus and HyperCap Target Enrichment Kit, sequenced on the MiSeq instrument. The results were analyzed using the BaseSpace Variant Interpreter and Integrative Genomics Viewer. All pathogenic and likely pathogenic variants were confirmed using Sanger sequencing. A total of 29 patients with hereditary ataxias were enrolled in the NGS testing, and 16 patients had a confirmed molecular diagnosis with diagnostic accuracy rate of 55.2%. Pathogenic or likely pathogenic mutations were identified in 10 different genes: POLG (PEOA1, n = 3; SCAE, n = 2), CACNA1A (EA2, n = 2), SACS (ARSACS, n = 2), SLC33A1 (SPG42, n = 2), STUB1 (SCA48, n = 1), SPTBN2 (SCA5, n = 1), TGM6 (SCA35, n = 1), SETX (AOA2, n = 1), ANO10 (SCAR10, n = 1), and SPAST (SPG4, n = 1). We demonstrated that an approach based on the targeted use of the NGS panel can be highly effective and a useful tool in the molecular diagnosis of ataxia patients. Furthermore, we highlight the fact that a sequencing panel targeting both ataxias and HSP genes increases the diagnostic success level.

摘要

遗传性共济失调(HA)是一组罕见的异质性疾病。在这里,我们报告了使用定制设计的下一代测序(NGS)面板对一组共济失调患者进行分子检测的结果。由于遗传性共济失调和痉挛性截瘫(HSP)的遗传和临床重叠,该面板同时包含 HA 和 HSP 基因。NGS 文库包含 152 个基因的编码序列,使用 KAPA HyperPlus 和 HyperCap Target Enrichment Kit 进行制备,在 MiSeq 仪器上进行测序。使用 BaseSpace Variant Interpreter 和 Integrative Genomics Viewer 分析结果。使用 Sanger 测序法对所有致病性和可能致病性的变体进行确认。共有 29 名遗传性共济失调患者接受了 NGS 检测,16 名患者获得了明确的分子诊断,诊断准确率为 55.2%。在 10 个不同的基因中发现了致病性或可能致病性的突变:POLG(PEOA1,n=3;SCAE,n=2)、CACNA1A(EA2,n=2)、SACS(ARSACS,n=2)、SLC33A1(SPG42,n=2)、STUB1(SCA48,n=1)、SPCN2(SCA5,n=1)、TGM6(SCA35,n=1)、SETX(AOA2,n=1)、ANO10(SCAR10,n=1)和 SPAST(SPG4,n=1)。我们证明,基于靶向使用 NGS 面板的方法可以非常有效,并且是分子诊断患者的有用工具。此外,我们强调了一个事实,即针对共济失调和 HSP 基因的测序面板可以提高诊断成功率。

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本文引用的文献

1
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Acta Neurol Belg. 2021 Dec;121(6):1823-1830. doi: 10.1007/s13760-020-01552-7. Epub 2020 Nov 26.
2
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.下一代测序研究揭示遗传性痉挛性截瘫及相关表型的更广泛变异谱。
Neurogenetics. 2019 Mar;20(1):27-38. doi: 10.1007/s10048-019-00565-6. Epub 2019 Feb 19.
3
Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant.
Tremor Other Hyperkinet Mov (N Y). 2024 Jan 8;14:2. doi: 10.5334/tohm.835. eCollection 2024.
4
Diagnostic Yield of NGS Tests for Hereditary Ataxia: a Systematic Review.遗传性共济失调的 NGS 检测的诊断率:系统评价。
Cerebellum. 2024 Aug;23(4):1552-1565. doi: 10.1007/s12311-023-01629-y. Epub 2023 Nov 11.
由于CACNA1A致病变异导致的主要家族内表型异质性和不完全外显率。
Eur J Med Genet. 2019 Jun;62(6):103530. doi: 10.1016/j.ejmg.2018.08.011. Epub 2018 Aug 22.
4
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.外显子组测序在散发性或家族性小脑共济失调临床诊断中的应用
JAMA Neurol. 2014 Oct;71(10):1237-46. doi: 10.1001/jamaneurol.2014.1944.
5
Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.SLC33A1 基因突变导致一种致命的常染色体隐性遗传病,其特征为先天性白内障、听力损失以及血清铜和铜蓝蛋白水平降低。
Am J Hum Genet. 2012 Jan 13;90(1):61-8. doi: 10.1016/j.ajhg.2011.11.030.
6
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.常染色体显性小脑共济失调:多聚谷氨酰胺扩展及其他。
Lancet Neurol. 2010 Sep;9(9):885-94. doi: 10.1016/S1474-4422(10)70183-6.
7
A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42).共 220 名常染色体显性痉挛性截瘫患者未显示 SLC33A1 基因(SPG42)突变。
Eur J Hum Genet. 2010 Sep;18(9):1065-7. doi: 10.1038/ejhg.2010.68. Epub 2010 May 12.
8
A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).编码乙酰辅酶A转运蛋白的SLC33A1基因中的错义突变会导致常染色体显性遗传性痉挛性截瘫(SPG42)。
Am J Hum Genet. 2008 Dec;83(6):752-9. doi: 10.1016/j.ajhg.2008.11.003.
9
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.一个近亲家庭中由三种不同基因缺陷导致的常染色体隐性共济失调。
J Neurogenet. 2008;22(2):139-48. doi: 10.1080/01677060802025233.
10
Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood.线粒体DNA耗竭是儿童期多种呼吸链缺陷的常见原因。
J Pediatr. 2007 May;150(5):531-4, 534.e1-6. doi: 10.1016/j.jpeds.2007.01.044.