TY - JOUR
T1 - Polymorphism screening of brain-expressed FABP7, 5 and 3 genes and association studies in autism and schizophrenia in Japanese subjects
AU - Maekawa, Motoko
AU - Iwayama, Yoshimi
AU - Arai, Ryoichi
AU - Nakamura, Kazuhiko
AU - Ohnishi, Tetsuo
AU - Toyota, Tomoko
AU - Tsujii, Masatsugu
AU - Okazaki, Yuji
AU - Osumi, Noriko
AU - Owada, Yuji
AU - Mori, Norio
AU - Yoshikawa, Takeo
PY - 2010/2
Y1 - 2010/2
N2 - 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, 376G>C (Val126Leu) in FABP7 and 340G>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 8A>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.
AB - 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, 376G>C (Val126Leu) in FABP7 and 340G>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 8A>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.
KW - Crystallographic analysis
KW - Fatty acid-binding protein
KW - Missense mutation
UR - http://www.scopus.com/inward/record.url?scp=77649107751&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77649107751&partnerID=8YFLogxK
U2 - 10.1038/jhg.2009.133
DO - 10.1038/jhg.2009.133
M3 - Article
C2 - 20057506
AN - SCOPUS:77649107751
SN - 1434-5161
VL - 55
SP - 127
EP - 130
JO - Journal of Human Genetics
JF - Journal of Human Genetics
IS - 2
ER -