五个Dysferlinopathy家系的DYSF基因变异分析  

Analysis of genetic variants in five pedigrees affected with Dysferlinopathy

作　　者：夏艳洁 时盼来 侯雅勤[1] 陈铎[1] 代鹏[1] 赵莘瑜[2] 孔祥东[1] Xia Yanjie;Shi Panlai;Hou Yaqin;Chen Duo;Dai Peng;Zhao Xinyu;Kong Xiangdong(Prenatal Diagnosis Center,the First Affiliated Hospital of Zhengzhou University,Zhengzhou,Henan 450052,China;Department of Neurology,the First Affiliated Hospital of Zhengzhou University,Zhengzhou,Henan 450052,China)

机构地区：[1]郑州大学第一附属医院产前诊断中心,450052 [2]郑州大学第一附属医院神经内科,450052

出　　处：《中华医学遗传学杂志》2021年第3期205-209,共5页Chinese Journal of Medical Genetics

基　　金：国家重点研发计划(2018YFC1002203)。

摘　　要：目的对5个Dysferlinopathy家系进行DYSF基因变异分析,明确其致病原因。方法应用高通量测序技术进行检测,确定可疑变异后应用Sanger测序进行变异位点验证,根据美国医学遗传学及基因组学学会(American College of Medical Genetics and Genomics,ACMG)遗传变异分类标准与指南对变异的致病性进行评估。结果高通量靶向测序和Sanger测序结果显示,5个Dysferlinopathy家系中共检测出10个DYSF基因变异位点(5个移码变异、3个剪切区变异、1个错义变异和1个无义变异)。其中c.1375dupA(p.Met459Asnfs*15)、c.610C>T(p.Arg204X)、c.1180+5G>A和c.1284+2T>C为已报道过的致病性变异,而c.4008_4010delCCTinsAC(p.Leu1337Argfs*8)、c.1137_1169del(p.379_390del)、c.754 A>G(p.Thr252Ala)、c.1175_1176insGCAGAGTG(p.Met394Serfs*7)、c.3114_3115insCGGC(p.Arg1040 Profs*74)和c.1053+3G>C为未报道过的新变异,根据ACMG遗传变异分类标准与指南,c.1137_1169del、c.1175_1176 insGCAGAGTG和c.3114_3115insCGGC为致病性变异(PVS1+PM2+PM3),c.4008_4010delCCTinsAC变异为可能致病性变异(PVS1+PM2),c.754A>G和c.1053+3G>C为意义不明确的变异(PM2+PM3+PP3)。结论DYSF基因变异可能为这5个Dysferlinopathy家系患者的致病原因,新变异的检出丰富了DYSF基因变异谱。Objective To analyze the clinical phenotype and genetic variants in five Chinese pedigrees affected with Dysferlinopathy.Methods Next generation sequencing(NGS)was carried out for the probands from the five pedigrees.Suspected variants were validated by Sanger sequencing.Pathogenicity of the variants was assessed based on the standards and guidelines by the American College of Medical Genetics and Genomics(ACMG).Results Ten DYSF gene variants(including 5 frameshift variants,3 splicing variants,1 missense variant and 1 nonsense variant)were detected.Among these,c.1375dupA(p.Met459Asnfs*15),c.610C>T(p.Arg204X),c.1180+5G>A and c.1284+2T>C were known to be pathogenic,while c.4008_4010delCCTinsAC(p.Leu1337Argfs*8),c.1137_1169del(p.379_390del),c.754 A>G(p.Thr252Ala),c.1175_1176insGCAGAGTG(p.Met394Serfs*7),c.3114_3115insCGGC(p.Arg1040 Profs*74)and c.1053+3G>C were unreported previously.Of the six novel variants,c.1137_1169del,c.1175_1176 insGCAGAGTG and c.3114_3115insCGGC were predicted as pathogenic(PVS1+PM2+PM3),c.4008_4010delCCTinsAC as likely pathogenic(PVS1+PM2),c.754A>G and c.1053+3G>C as variants of uncertain significance based on the ACMG standards and guidelines.Conclusion Variants of the DYSF gene probably underlay Dysferlinopathy in the patients among the five pedigrees.Above finding has enriched the spectrum of DYSF gene variants.

关 键 词：Dysfer肌病 DYSF基因 高通量测序 复合杂合变异 

分 类 号：R681[医药卫生—骨科学]