Mutations of ANK3 identified by exome sequencing are associated with Autism susceptibility

被引：97

作者：

Bi, Cheng ^{[2
,3
]}

Wu, Jinyu ^{[1
]}

Jiang, Tao ^{[4
]}

Liu, Qi ^{[1
]}

Cai, Wanshi ^{[1
]}

Yu, Ping ^{[1
]}

Cai, Tao ^{[1
,6
]}

Zhao, Mei ^{[2
]}

Jiang, Yong-hui ^{[5
]}

Sun, Zhong Sheng ^{[1
,6
]}

机构：

[1] Wenzhou Med Coll, Inst Genom Med, Wenzhou, Peoples R China

[2] Chinese Acad Sci, Inst Psychol, Beijing 100101, Peoples R China

[3] Chinese Acad Sci, Grad Univ, Beijing, Peoples R China

[4] Beijing Genom Inst Shenzhen, Shenzhen, Peoples R China

[5] Duke Univ, Sch Med, Dept Pediat & Neurobiol, Durham, NC USA

[6] Chinese Acad Sci, Beijing Inst Life Sci, Beijing, Peoples R China

来源：

HUMAN MUTATION | 2012年 / 33卷 / 12期

关键词：

autism spectrum disorder; de novo mutation; Ankyrin; 3; susceptibility; whole-exome sequencing; DE-NOVO MUTATIONS; SPECTRUM DISORDERS; GENETICS; NETWORK;

D O I：

10.1002/humu.22174

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Autism spectrum disorders (ASDs) are common neurodevelopmental disorders with a strong genetic etiology. However, due to the extreme genetic heterogeneity of ASDs, traditional approaches for gene discovery are challenging. Next-generation sequencing technologies offer an opportunity to accelerate the identification of the genetic causes of ASDs. Here, we report the results of whole-exome sequence in a cohort of 20 ASD patients. By extensive bioinformatic analysis, we identified novel mutations in seven genes that are implicated in synaptic function and neurodevelopment. After sequencing an additional 47 ASD samples, we identified three different missense mutations in ANK3 in four unrelated ASD patients, one of which, c.4705T>G (p.S1569A), is a de novo mutation. Given the fact that ANK3 has been shown to strongly associate with schizophrenia and bipolar disorder, our findings support an association between ANK3 mutations and ASD susceptibility and imply a shared molecular pathophysiology between ASDs and other neuropsychiatric disorders. Hum Mutat 33:16351638, 2012. (c) 2012 Wiley Periodicals, Inc.

引用

页码：1635 / 1638

页数：4

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