Resequencing and association study of the NFKB activating protein-like gene (NKAPL) in schizophrenia

被引:13
作者
Chen, Shih-Fen [1 ,2 ]
Chao, Yu-Lin [3 ,4 ]
Shen, Yu-Chih [3 ,4 ]
Chen, Chia-Hsiang [5 ,6 ]
Weng, Ching-Feng [1 ,2 ]
机构
[1] Natl Dong Hwa Univ, Dept Life Sci, Shoufeng 97401, Hualien, Taiwan
[2] Natl Dong Hwa Univ, Inst Biotechnol, Shoufeng 97401, Hualien, Taiwan
[3] Tzu Chi Gen Hosp, Dept Psychiat, Hualien 970, Taiwan
[4] Tzu Chi Univ, Sch Med, Hualien, Taiwan
[5] Chang Gung Mem Hosp Linkou, Dept Psychiat, Taoyuan, Taiwan
[6] Chang Gung Univ, Sch Med, Taoyuan, Taiwan
关键词
NKAPL; Schizophrenia; rs1635; Han Chinese; GENOME-WIDE ASSOCIATION; MULTIPLE RARE ALLELES; HAN CHINESE; DETERMINANTS; MUTATIONS; VARIANTS; MODEL;
D O I
10.1016/j.schres.2014.05.038
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objectives: Schizophrenia is a highly inheritable disorder, but many aspects of its etiology and pathophysiology remain poorly understood. Recently, in the Han Chinese population, a SNP rs1635 located within the exon of the NKAPL gene (encoding NFKB activating protein-like) achieved genome-wide significance in schizophrenia. Methods: In order to find the causal variants of the NKAPL gene in schizophrenia, we searched for genetic variants in the promoter region, and exons (including both UTR ends) using direct sequencing in a sample of patients with schizophrenia (n = 515) and non-psychotic controls (n = 456), all Han Chinese from Taiwan, and conducted an association and rudimentary functional study. Results: We identified 5 common SNPs (defined as minor allele frequency (MAF) > 0.01) in the NKAPL gene. In a case-control association analysis, the minor allele (A) of rs1635 was significantly more common among patients than controls (P = 0.0003, OR = 1.41, 95% CI = 1.17-1.71). A haplotype analysis of the 5 common SNPs indicated a risk haplotype (rs12000C-rs1635A-rs9461446C-rs3734564G-rs1679709G) associated with schizophrenia (P = 2.77e-005, OR = 1.53, 95% CI = 1.25-1.87). In addition, we identified 4 patient-specific rare SNPs (MAF < 0.01) (c.137G > A, c.213G > A, c.752C > T (rs370337122), and c.844G > A (rs147161729)) within the NKAPL gene. In silico analysis demonstrated their functional impact on the protein; however, there was also 1 control-specific rare SNP (c.119G > A) detected within the NKAPL gene, indicating that the clinical relevance of these putatively pathological rare SNPs is not straightforward. Conclusions: This study suggested that rs1635 in the NKAPL gene appeared to play a role in conferring susceptibility to schizophrenia. In addition, some rare SNPs in the NKAPL gene with possibly damaging effects may be important in our patients. Our study provides genetic clues to indicate the involvement of NKAPL in schizophrenia. (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:169 / 174
页数:6
相关论文
共 26 条
[1]   A method and server for predicting damaging missense mutations [J].
Adzhubei, Ivan A. ;
Schmidt, Steffen ;
Peshkin, Leonid ;
Ramensky, Vasily E. ;
Gerasimova, Anna ;
Bork, Peer ;
Kondrashov, Alexey S. ;
Sunyaev, Shamil R. .
NATURE METHODS, 2010, 7 (04) :248-249
[2]  
[Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
[3]   Neurodevelopment, neuroplasticity, and new genes for schizophrenia [J].
Arnold, SE ;
Talbot, K ;
Hahn, CG .
DEVELOPMENT, DYNAMICS AND PATHOLOGY OF NEURONAL NETWORKS: FROM MOLECULES TO FUNCTIONAL CIRCUITS, 2005, 147 :319-345
[4]   Haploview: analysis and visualization of LD and haplotype maps [J].
Barrett, JC ;
Fry, B ;
Maller, J ;
Daly, MJ .
BIOINFORMATICS, 2005, 21 (02) :263-265
[5]   Listening to silence and understanding nonsense: Exonic mutations that affect splicing [J].
Cartegni, L ;
Chew, SL ;
Krainer, AR .
NATURE REVIEWS GENETICS, 2002, 3 (04) :285-298
[6]   Genetic Structure of the Han Chinese Population Revealed by Genome-wide SNP Variation [J].
Chen, Jieming ;
Zheng, Houfeng ;
Bei, Jin-Xin ;
Sun, Liangdan ;
Jia, Wei-hua ;
Li, Tao ;
Zhang, Furen ;
Seielstad, Mark ;
Zeng, Yi-Xin ;
Zhang, Xuejun ;
Liu, Jianjun .
AMERICAN JOURNAL OF HUMAN GENETICS, 2009, 85 (06) :775-785
[7]   Phenotypic and genetic complexity of psychosis - Invited commentary on ... Schizophrenia: a common disease caused by multiple rare alleles [J].
Craddock, Nick ;
O'Donovan, Michael C. ;
Owen, Michael J. .
BRITISH JOURNAL OF PSYCHIATRY, 2007, 190 :200-203
[8]   Rare Variants Create Synthetic Genome-Wide Associations [J].
Dickson, Samuel P. ;
Wang, Kai ;
Krantz, Ian ;
Hakonarson, Hakon ;
Goldstein, David B. .
PLOS BIOLOGY, 2010, 8 (01)
[9]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229
[10]   The International HapMap Project [J].
Gibbs, RA ;
Belmont, JW ;
Hardenbol, P ;
Willis, TD ;
Yu, FL ;
Yang, HM ;
Ch'ang, LY ;
Huang, W ;
Liu, B ;
Shen, Y ;
Tam, PKH ;
Tsui, LC ;
Waye, MMY ;
Wong, JTF ;
Zeng, CQ ;
Zhang, QR ;
Chee, MS ;
Galver, LM ;
Kruglyak, S ;
Murray, SS ;
Oliphant, AR ;
Montpetit, A ;
Hudson, TJ ;
Chagnon, F ;
Ferretti, V ;
Leboeuf, M ;
Phillips, MS ;
Verner, A ;
Kwok, PY ;
Duan, SH ;
Lind, DL ;
Miller, RD ;
Rice, JP ;
Saccone, NL ;
Taillon-Miller, P ;
Xiao, M ;
Nakamura, Y ;
Sekine, A ;
Sorimachi, K ;
Tanaka, T ;
Tanaka, Y ;
Tsunoda, T ;
Yoshino, E ;
Bentley, DR ;
Deloukas, P ;
Hunt, S ;
Powell, D ;
Altshuler, D ;
Gabriel, SB ;
Qiu, RZ .
NATURE, 2003, 426 (6968) :789-796