A Novel Missense Mutation in Peripheral Myelin Protein-22 Causes Charcot-Marie-Tooth Disease

• Published in: Chinese medical journal Vol. 130; no. 15; pp. 1779 - 1784
• Main Authors: Li, Li-Xi, Dong, Hai-Lin, Xiao, Bao-Guo, Wu, Zhi-Ying
• Format: Journal Article
• Language: English
• Published: China Medknow Publications and Media Pvt. Ltd 05.08.2017; Lippincott Williams & Wilkins Ovid Technologies; Department of Neurology and Institute of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai 200040, China%Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, The Collaborative Innovation Center for Brain Science, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310009, China; Medknow Publications & Media Pvt Ltd; Wolters Kluwer
• Subjects: Adult; Aged; Apoptosis; Charcot-Marie-Tooth Disease; Endoplasmic Reticulum; Missense Mutation; Peripheral Myelin Protein-22; Charcot-Marie-Tooth disease; Charcot-Marie-Tooth Disease - genetics; CMT; Development and progression; Disease; DNA sequencing; Female; Gene mutation; Genes; Genetic aspects; Genotype & phenotype; HeLa Cells; High-Throughput Nucleotide Sequencing; Hospitals; Humans; Male; Middle Aged; Mutation; Mutation - genetics; Mutation, Missense - genetics; Myelin proteins; Myelin Proteins - genetics; Nervous system; Neurology; Original; Patients; Pedigree; Peripheral neuropathy; Phenotypes; Plasmids; Point Mutation - genetics; Proteins; Software; Studies; Variance analysis; 医学遗传学; 周围神经; 常染色体; 疾病; 突变体蛋白; 致病基因; 髓鞘; United States > US; California; Missense Mutation; Endoplasmic Reticulum; Peripheral Myelin Protein-22; Apoptosis; Charcot-Marie-Tooth Disease
• ISSN: 0366-6999; 2542-5641
• DOI: 10.4103/0366-6999.211539

Background：Charcot-Marie-Tooth disease （CMT） is the most common inherited peripheral neuropathy.A great number of causative genes have been described in CMT,and among them,the heterozygous duplication of peripheral myelin protein-22 （PMP22） is the major cause.Although the missense mutation in PMP22 is rarely reported,it has been demonstrated to be associated with CMT.This study described a novel missense mutation of PMP22 in a Chinese family with CMT phenotype.Methods：Targeted next-generation sequencing （NGS） was used to screen the causative genes in a family featured with an autosomal dominant demyelinating form of CMT.The potential variants identified by targeted NGS were verified by Sanger sequencing and classified according to the American College of Medical Genetics and Genomics standards and guidelines.Further cell transfection studies were performed to characterize the function of the novel variant.Results：Using targeted NGS,a novel heterozygous missense variant in PMP22 （c.320G〉A,p.G107D） was identified.In vitro cell functional studies revealed that mutant PMP22 protein carrying p.G 107D mutation lost the ability to reach the plasma membrane,was mainly retained in the endoplasmic reticulum,and induced cell apoptosis.Conclusions：This study supported the notion that missense mutations in PMP22 give rise to a CMT phenotype,possibly through a toxic gain-of-function mechanism.