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Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia
Tang, Jinsong1,2,3; Fan, Yu4; Li, Hong1,2,3,15; Xiang, Qun4,5; Zhang, Deng-Feng4; Li, Zongchang1,2,3; He, Ying1,2,3; Liao, Yanhui1,2,3; Wang, Ya6,7; He, Fan8,9,10; Zhang, Fengyu1,2,3; Shugart, Yin Yao11; Liu, Chunyu12; Tang, Yanqing13; Chan, Raymond C. K.6,7; Wang, Chuan-Yue8,9,10; Yao, Yong-Gang4,5,14; Chen, Xiaogang1,2,3
2017-06-20
发表期刊JOURNAL OF GENETICS AND GENOMICS
ISSN1673-8527
文章类型Article
卷号44期号:6页码:295-306
摘要

Schizophrenia is a common disorder with a high heritability, but its genetic architecture is still elusive. We implemented whole-genome sequencing (WGS) analysis of 8 families with monozygotic (MZ) twin pairs discordant for schizophrenia to assess potential association of de novo mutations (DNMs) or inherited variants with susceptibility to schizophrenia. Eight non-synonymous DNMs (including one splicing site) were identified and shared by twins, which were either located in previously reported schizophrenia risk genes (p. V24689I mutation in TTN, p. S2506T mutation in GCN1L1, IVS3+1G > T in DOCK1) or had a benign to damaging effect according to in silico prediction analysis. By searching the inherited rare damaging or loss-of-function (LOF) variants and common susceptible alleles from three classes of schizophrenia candidate genes, we were able to distill genetic alterations in several schizophrenia risk genes, including GAD1, PLXNA2, RELN and FEZ1. Four inherited copy number variations (CNVs; including a large deletion at 16p13.11) implicated for schizophrenia were identified in four families, respectively. Most of families carried both missense DNMs and inherited risk variants, which might suggest that DNMs, inherited rare damaging variants and common risk alleles together conferred to schizophrenia susceptibility. Our results support that schizophrenia is caused by a combination of multiple genetic factors, with each DNM/variant showing a relatively small effect size. Copyright (C) 2017, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Limited and Science Press. All rights reserved.

关键词Whole-genome sequencing Schizophrenia Monozygotic twin De novo mutation Combined effect Susceptibility
DOI10.1016/j.jgg.2017.05.005
收录类别SCI
语种英语
项目资助者Strategic Priority Research Program of the Chinese Academy of Sciences(XDB02020003 ; Bureau of Frontier Sciences and Education, Chinese Academy of Sciences(QYZDJ-SSW-SMC005) ; National Natural Science Foundation of China(81088001 ; Beijing Training Project for the Leading Talents in S T(Z151100000315020) ; National Key Basic Research and Development Program (973)(2012CB517904) ; CAS/SAFEA International Partnership Programme for Creative Research Teams(Y2CX131003) ; XDB02030002) ; 81271484 ; 81471361 ; 81371480)
WOS研究方向Biochemistry & Molecular Biology ; Genetics & Heredity
WOS类目Biochemistry & Molecular Biology ; Genetics & Heredity
WOS记录号WOS:000404557900002
WOS标题词Science & Technology ; Life Sciences & Biomedicine
关键词[WOS]DE-NOVO MUTATIONS ; STRUCTURAL VARIANT DISCOVERY ; WIDE ASSOCIATION ; PSYCHIATRIC-DISORDERS ; SYNAPTIC PLASTICITY ; DISEASE MECHANISMS ; BIPOLAR DISORDER ; PROTEIN FUNCTION ; COMPLEX TRAITS ; MESSENGER-RNA
引用统计
被引频次:3[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.psych.ac.cn/handle/311026/21599
专题中国科学院心理健康重点实验室
作者单位1.Cent S Univ, Natl Clin Res Ctr Mental Hlth Disorders, Inst Mental Hlth, Xiangya Hosp 2, Changsha 410011, Hunan, Peoples R China
2.Cent S Univ, Xiangya Hosp 2, Natl Technol Inst Psychiat, Changsha 410011, Hunan, Peoples R China
3.Cent S Univ, Xiangya Hosp 2, Key Lab Psychiat & Mental Hlth Hunan Prov, Changsha 410011, Hunan, Peoples R China
4.Chinese Acad Sci & Yunnan Prov, Key Lab Anim Models & Human Dis Mech, Kunming Inst Zool, Kunming 650223, Peoples R China
5.Univ Chinese Acad Sci, Kunming Coll Life Sci, Kunming 650204, Peoples R China
6.Chinese Acad Sci, Neuropsychol & Appl Cognit Neurosci Lab, Inst Psychol, Beijing 100101, Peoples R China
7.Chinese Acad Sci, CAS Key Lab Mental Hlth, Inst Psychol, Beijing 100101, Peoples R China
8.Capital Med Univ, Beijing Key Lab Mental Disorders, Dept Psychiat, Beijing Anding Hosp, Beijing 100088, Peoples R China
9.Capital Med Univ, Ctr Schizophrenia, Beijing Inst Brain Disorders, Minist Sci & Technol, Beijing 100088, Peoples R China
10.Capital Med Univ, Lab Brain Disorders, Minist Sci & Technol, Beijing 100088, Peoples R China
11.NIMH, Unit Stat Genom, Intramural Res Programs, NIH, Bethesda, MD 20892 USA
12.Univ Illinois, Inst Human Genet, Chicago, IL 60607 USA
13.China Med Univ, Affiliated Hosp 1, Dept Psychiat, Shenyang 110122, Peoples R China
14.Chinese Acad Sci, CAS Ctr Excellence Brain Sci & Intelligence Techn, Shanghai 200031, Peoples R China
15.Zhengzhou Univ, Affiliated Hosp 1, Dept Psychiat, Zhengzhou 450052, Peoples R China
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Tang, Jinsong,Fan, Yu,Li, Hong,et al. Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia[J]. JOURNAL OF GENETICS AND GENOMICS,2017,44(6):295-306.
APA Tang, Jinsong.,Fan, Yu.,Li, Hong.,Xiang, Qun.,Zhang, Deng-Feng.,...&Chen, Xiaogang.(2017).Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia.JOURNAL OF GENETICS AND GENOMICS,44(6),295-306.
MLA Tang, Jinsong,et al."Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia".JOURNAL OF GENETICS AND GENOMICS 44.6(2017):295-306.
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