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全外显子组测序提高遗传性周围神经病的基因诊断。

Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.

机构信息

Northcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia.

Molecular Medicine Laboratory, Concord Hospital Sydney, Australia.

出版信息

Mol Genet Genomic Med. 2015 Mar;3(2):143-54. doi: 10.1002/mgg3.126. Epub 2015 Jan 14.

Abstract

Inherited peripheral neuropathies (IPNs) are a group of related diseases primarily affecting the peripheral motor and sensory neurons. They include the hereditary sensory neuropathies (HSN), hereditary motor neuropathies (HMN), and Charcot-Marie-Tooth disease (CMT). Using whole-exome sequencing (WES) to achieve a genetic diagnosis is particularly suited to IPNs, where over 80 genes are involved with weak genotype-phenotype correlations beyond the most common genes. We performed WES for 110 index patients with IPN where the genetic cause was undetermined after previous screening for mutations in common genes selected by phenotype and mode of inheritance. We identified 41 missense sequence variants in the known IPN genes in our cohort of 110 index patients. Nine variants (8%), identified in the genes MFN2, GJB1, BSCL2, and SETX, are previously reported mutations and considered to be pathogenic in these families. Twelve novel variants (11%) in the genes NEFL, TRPV4, KIF1B, BICD2, and SETX are implicated in the disease but require further evidence of pathogenicity. The remaining 20 variants were confirmed as polymorphisms (not causing the disease) and are detailed here to help interpret sequence variants identified in other family studies. Validation using segregation, normal controls, and bioinformatics tools was valuable as supporting evidence for sequence variants implicated in disease. In addition, we identified one SETX sequence variant (c.7640T>C), previously reported as a putative mutation, which we have confirmed as a nonpathogenic rare polymorphism. This study highlights the advantage of using WES for genetic diagnosis in highly heterogeneous diseases such as IPNs and has been particularly powerful in this cohort where genetic diagnosis could not be achieved due to phenotype and mode of inheritance not being previously obvious. However, first tier testing for common genes in clinically well-defined cases remains important and will account for most positive results.

摘要

遗传性周围神经病(IPN)是一组主要影响周围运动和感觉神经元的相关疾病。它们包括遗传性感觉神经病(HSN)、遗传性运动神经病(HMN)和夏科-马里-图病(CMT)。使用全外显子组测序(WES)进行基因诊断特别适合于 IPN,其中超过 80 个基因与最常见基因之外的弱基因型-表型相关性有关。我们对 110 名遗传性周围神经病患者进行了 WES 检测,这些患者在之前根据表型和遗传方式选择常见基因进行突变筛查后,遗传原因仍未确定。我们在 110 名索引患者的队列中发现了已知 IPN 基因中的 41 个错义序列变异。在 MFN2、GJB1、BSCL2 和 SETX 基因中发现的 9 个变异(8%)是以前报道的突变,被认为在这些家族中具有致病性。在 NEFL、TRPV4、KIF1B、BICD2 和 SETX 基因中发现的 12 个新变异(11%)与疾病有关,但需要进一步的致病性证据。其余 20 个变异被确认为多态性(不引起疾病),并在此详细说明,以帮助解释其他家族研究中发现的序列变异。使用分离、正常对照和生物信息学工具进行验证是支持疾病相关序列变异的有价值证据。此外,我们还鉴定了一个 SETX 序列变异(c.7640T>C),之前被报道为一个假定的突变,我们已经证实它是一个非致病性的罕见多态性。这项研究强调了在高度异质性疾病(如 IPN)中使用 WES 进行基因诊断的优势,并且在由于表型和遗传方式以前不明显而无法进行基因诊断的情况下,该队列特别有效。然而,在临床上定义明确的病例中进行常见基因的一级检测仍然很重要,并且将占大多数阳性结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fd/4367087/0507a1e11666/mgg30003-0143-f1.jpg

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