目标区域捕获测序检测常染色体隐性遗传性腓骨肌萎缩症GDAP1基因突变

研究背景腓骨肌萎缩症存在高度临床和遗传异质性,传统基因检测需对众多候选基因逐一筛查,存在效率低、耗时、费力等局限性。本文旨在探讨目标区域捕获测序技术诊断常染色体隐性遗传性腓骨肌萎缩症的可行性。方法采集5例临床拟诊常染色体隐性遗传性腓骨肌萎缩症患者的临床资料和外周血样本,采用目标区域捕获测序技术筛查腓骨肌萎缩症相关基因突变,Sanger测序对候选变异位点在患者及其父母外周血样本中进行验证。结果目标区域捕获测序显示,2例检出GDAP1基因复合杂合突变,余3例未检出致病性突变。经Sanger测序证实2例患儿存在GDAP1基因突变,例1为GDAP1基因复合杂合突变c.767A〉G（p.His256Ar...

Full description

Saved in:
Bibliographic Details
Published in中国现代神经疾病杂志 Vol. 17; no. 8; pp. 603 - 608
Main Author 何瑾 许国荣 林涵 王柠 陈万金
Format Journal Article
LanguageChinese
Published 福建医科大学附属第一医院神经内科,福州,350005 2017
Subjects
基因
夏科-马里-图斯病
突变
系谱
隐性
Genes,recessive
Pedigree
Charcot-Marie-Tooth disease
夏科-马里-图斯病
突变
系谱
Mutation
基因,隐性
Online AccessGet full text
ISSN1672-6731
DOI10.3969/j.issn.1672-6731.2017.08.009

Cover

More Information
Summary:研究背景腓骨肌萎缩症存在高度临床和遗传异质性,传统基因检测需对众多候选基因逐一筛查,存在效率低、耗时、费力等局限性。本文旨在探讨目标区域捕获测序技术诊断常染色体隐性遗传性腓骨肌萎缩症的可行性。方法采集5例临床拟诊常染色体隐性遗传性腓骨肌萎缩症患者的临床资料和外周血样本,采用目标区域捕获测序技术筛查腓骨肌萎缩症相关基因突变,Sanger测序对候选变异位点在患者及其父母外周血样本中进行验证。结果目标区域捕获测序显示,2例检出GDAP1基因复合杂合突变,余3例未检出致病性突变。经Sanger测序证实2例患儿存在GDAP1基因突变,例1为GDAP1基因复合杂合突变c.767A〉G（p.His256Arg）和c.866T〉A（p.Phe289Tyr）,其父携带c.866T〉A（p.Phe289Tyr）突变,其母携带c.767A〉G（p.His256Arg）突变;例2为GDAP1基因复合杂合突变c.571C〉T（p.Arg191X）和c.589del C（p.Asp198IlefsX8）,其父携带c.589del C（p.Asp198IlefsX8）突变,其母携带c.571C〉T（p.Arg191X）突变,最终明确诊断为常染色体隐性遗传性腓骨肌萎缩症。结论目标区域捕获测序技术是一项高效基因检测方法,适用于常染色体隐性遗传性腓骨肌萎缩症的基因诊断。
Bibliography:Charcot-Marie-Tooth disease; Genes; recessive; Mutation; Pedigree
Background Owing to the clinical variability and molecular heterogeneity,the traditional Sanger sequencing takes time and effort and is inefficient.In this paper,target region capture sequencing in the diagnosing of autosomal recessive Charcot-Marie-Tooth disease（AR-CMT） is explored.Methods Clinical data and peripheral blood sample of 5 clinically suspected AR.CMT patients were collected.Charcot-Marie-Tooth disease（CMT） related gene mutation were detected by target region capture sequencing.The candidate variants were confirmed in the peripheral blood sample of the patients and their parents by Sanger sequencing.Results Target region capture sequencing revealed that compound heterozygous mutations of GDAP1 gene was found in 2 patients,and was not seen in the other 3 patients.Sanger sequencing revealed that among the 2 patients with mutation of GDAP1 gene,compound heterozygous mutation c.767A G（p.His256Arg） and c.866T A（p.Phe289Tyr） were seen in
ISSN:1672-6731
DOI:10.3969/j.issn.1672-6731.2017.08.009