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A Two-Stage Association Study Suggests BRAP as a Susceptibility Gene for Schizophrenia
Author(s) -
Fuquan Zhang,
Chenxing Liu,
Yong Xu,
Guoyang Qi,
Guozhen Yuan,
Zaohuo Cheng,
Jidong Wang,
Guoqiang Wang,
Zhiqiang Wang,
Wei Zhu,
Zhenhe Zhou,
Xingfu Zhao,
Lin Tian,
Chunhui Jin,
Janmin Yuan,
Guofu Zhang,
Yaguang Chen,
Lifang Wang,
Tianlan Lu,
Hao Yan,
Yanyan Ruan,
Weihua Yue,
Dai Zhang
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0086037
Subject(s) - single nucleotide polymorphism , biology , genome wide association study , population , genetics , genotype , gene , medicine , environmental health
Schizophrenia (SZ) is a neurodevelopmental disorder in which altered immune function typically plays an important role in mediating the effect of environmental insults and regulation of inflammation. The breast cancer suppressor protein associated protein (BRAP) is suggested to exert vital effects in neurodevelopment by modulating the mitogen-activated protein kinase cascade and inflammation signaling. To explore the possible role of BRAP in SZ, we conducted a two-stage study to examine the association of BRAP polymorphisms with SZ in the Han Chinese population. In stage one, we screened SNPs in BRAP from our GWAS data, which detected three associated SNPs, with rs3782886 being the most significant one (P  =  2.31E-6, OR  =  0.67). In stage two, we validated these three SNPs in an independently collected population including 1957 patients and 1509 controls, supporting the association of rs3782886 with SZ (P  =  1.43E-6, OR  =  0.73). Furthermore, cis-eQTL analysis indicates that rs3782886 genotypes are associated with mRNA levels of aldehyde dehydrogenase 2 family (ALDH2) (P  =  0.0039) and myosin regulatory light chain 2 (MYL2) (P < 1.0E-4). Our data suggest that the BRAP gene may confer vulnerability for SZ in Han Chinese population, adding further evidence for the involvement of developmental and/or neuroinflammatory cascades in the illness.

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