Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects

被引:35
|
作者
Maekawa, Motoko [1 ]
Iwayama, Yoshimi [1 ]
Arai, Ryoichi [2 ]
Nakamura, Kazuhiko [3 ]
Ohnishi, Tetsuo [1 ]
Toyota, Tomoko [1 ]
Tsujii, Masatsugu [4 ]
Okazaki, Yuji [5 ]
Osumi, Noriko [6 ,7 ]
Owada, Yuji [8 ]
Mori, Norio [3 ]
Yoshikawa, Takeo [1 ,7 ]
机构
[1] RIKEN, Lab Mol Psychiat, Brain Sci Inst, Wako, Saitama 3510198, Japan
[2] Shinshu Univ, Int Young Researchers Empowerment Ctr, Nagano, Japan
[3] Hamamatsu Univ Sch Med, Dept Psychiat & Neurol, Shizuoka, Japan
[4] Chukyo Univ, Fac Sociol, Aichi, Japan
[5] Tokyo Metropolitan Matsuzawa Hosp, Tokyo, Japan
[6] Tohoku Univ, Grad Sch Med, Dept Dev Neurobiol, Sendai, Miyagi 980, Japan
[7] Japanese Sci & Technol Agcy, CREST, Tokyo, Japan
[8] Yamaguchi Univ, Grad Sch Med, Dept Organ Anat, Yamaguchi, Japan
关键词
crystallographic analysis; fatty acid-binding protein; missense mutation; ACID-BINDING PROTEIN;
D O I
10.1038/jhg.2009.133
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fatty acid-binding protein (FABP) gene family encode fatty acid-binding proteins and consist of at least 12 members, of which FABP7, 5 and 3 are expressed in the brain. We previously showed that FABP7 is associated with schizophrenia and bipolar disorder. Recently, genetic overlap between autism and schizophrenia has been reported. Therefore, in this study, we set out to examine the possible roles of brain-expressed FABPs in autism, focusing primarily on potentially functional polymorphisms (that is, missense polymorphisms). First, we resequenced the three genes using 285 autism samples. We identified 13 polymorphisms, of which 7 are novel. Of the novel single-nucleotide polymorphisms (SNPs), two are missense mutations, namely, 376G4>C (Val126Leu) in FABP7 and 340G4>C (Gly114Arg) in FABP5. Second, we tested for the genetic association of four missense SNPs with autism and schizophrenia, but failed to detect significant results. Finally, as a web-based algorithm predicts that the 8A4>G (Asp3Gly; rs17848124) in FABP3 is 'probably damaging', we estimated the possible impact of this SNP, and found that the loss of charge and salt bridge, caused by the Asp3-to-Gly3, may affect stability of the FABP3 protein. Future searches for associated phenotypes with missense SNPs using larger samples are highly warranted. Journal of Human Genetics (2010) 55, 127-130; doi: 10.1038/jhg.2009.133; published online 8 January 2010
引用
收藏
页码:127 / 130
页数:4
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