中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss

文献类型:期刊论文

作者Zhao, Yali1; Zhao, Feifan1; Zong, Liang1; Zhang, Peng2; Guan, Liping2; Zhang, Jianguo2,3; Wang, Dayong1; Wang, Jing4; Chai, Wei5; Lan, Lan1
刊名PLOS ONE
出版日期2013
卷号8期号:7
ISSN号1932-6203
产权排序4
通讯作者Wang, QJ (reprint author), Chinese Peoples Liberat Army Gen Hosp, Inst Otolaryngol, Dept Otorhinolaryngol Head & Neck Surg, Beijing, Peoples R China.
英文摘要In this study, a five-generation Chinese family (family F013) with progressive autosomal dominant hearing loss was mapped to a critical region spanning 28.54 Mb on chromosome 9q31.3-q34.3 by linkage analysis, which was a novel DFNA locus, assigned as DFNA56. In this interval, there were 398 annotated genes. Then, whole exome sequencing was applied in three patients and one normal individual from this family. Six single nucleotide variants and two indels were found co-segregated with the phenotypes. Then using mass spectrum (Sequenom, Inc.) to rank the eight sites, we found only the TNC gene be co-segregated with hearing loss in 53 subjects of F013. And this missense mutation (c.5317G>A, p.V1773M) of TNC located exactly in the critical linked interval. Further screening to the coding region of this gene in 587 subjects with nonsyndromic hearing loss (NSHL) found a second missense mutation, c.5368A>T (p. T1796S), co-segregating with phenotype in the other family. These two mutations located in the conserved region of TNC and were absent in the 387 normal hearing individuals of matched geographical ancestry. Functional effects of the two mutations were predicted using SIFT and both mutations were deleterious. All these results supported that TNC may be the causal gene for the hearing loss inherited in these families. TNC encodes tenascin-C, a member of the extracellular matrix (ECM), is present in the basilar membrane (BM), and the osseous spiral lamina of the cochlea. It plays an important role in cochlear development. The up-regulated expression of TNC gene in tissue repair and neural regeneration was seen in human and zebrafish, and in sensory receptor recovery in the vestibular organ after ototoxic injury in birds. Then the absence of normal tenascin-C was supposed to cause irreversible injuries in cochlea and caused hearing loss.
学科主题Physiological psychology/Biological Psychology
收录类别SCI
项目简介This work was supported by the grants of the National Natural Science Foundation of China, Major Project, No. 81120108009 and National Natural Science Foundation of Youth Science Foundation No.81100719. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
原文出处http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728356/pdf/pone.0069549.pdf
语种英语
WOS记录号WOS:000323114200039
源URL[http://ir.psych.ac.cn/handle/311026/10629]  
专题心理研究所_中国科学院心理健康重点实验室
作者单位1.Chinese Peoples Liberat Army Gen Hosp, Inst Otolaryngol, Dept Otorhinolaryngol Head & Neck Surg, Beijing, Peoples R China
2.BGI Shenzhen, Shenzhen, Peoples R China
3.Fudan Univ, T Life Res Ctr, Shanghai 200433, Peoples R China
4.Chinese Acad Sci, Inst Psychol, Key Lab Mental Hlth, Beijing 100101, Peoples R China
5.Chinese Peoples Liberat Army Gen Hosp, Dept Orthopaed Surg, Beijing, Peoples R China
6.BGI Tianjin, Tianjin, Peoples R China
7.S China Univ Technol, Sch Biosci & Biotechnol, Guangzhou, Guangdong, Peoples R China
8.China Agr Univ, Coll Biol Sci, State Key Lab AgroBiotechnol, Beijing 100094, Peoples R China
9.Chinese Peoples Liberat Army Gen Hosp, Inst Life Sci, Beijing, Peoples R China
10.Coll France, F-75231 Paris, France
推荐引用方式
GB/T 7714
Zhao, Yali,Zhao, Feifan,Zong, Liang,et al. Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss[J]. PLOS ONE,2013,8(7).
APA Zhao, Yali.,Zhao, Feifan.,Zong, Liang.,Zhang, Peng.,Guan, Liping.,...&Wang, Qiuju.(2013).Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss.PLOS ONE,8(7).
MLA Zhao, Yali,et al."Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss".PLOS ONE 8.7(2013).

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来源:心理研究所

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