TY - JOUR
T1 - Exon 3 of tyrosine hydroxylase gene
T2 - Lack of association with Japanese schizophrenic patients
AU - Ota, M.
AU - Nakashima, A.
AU - Ikemoto, K.
AU - Nojima, S.
AU - Tanaka, M.
AU - Okuda, M.
AU - Koga, H.
AU - Mori, K.
AU - Kaneko, Y. S.
AU - Fujiwara, K.
AU - Yamamoto, H.
AU - Nagatsu, T.
AU - Ota, A.
N1 - Funding Information:
We would like to express our gratitude to all patients and control individuals for their participation in this study. We also thank to Dr Y Ono (Fujita Health University) for his critical reading of the manuscript. This study was supported by grants-in-aid from Fujita Health University, Japan, to A Ota.
PY - 2001
Y1 - 2001
N2 - Tyrosine hydroxylase (TH) is the rate-limiting enzyme in dopamine (DA) biosynthesis. Exon 3 of the human TH gene encodes the sequence from Set31 to Glu104 of type 1 enzyme, which contains the critical parts for regulation of the catalytic activity. The amino acid residues Gly36-Arg37-Arg38 were identified as a key sequence for DA to exert its inhibitory effect on catalytic activity. Therefore, we screened the nucleotide sequences of exon 3 from 201 Japanese patients with schizophrenia to explain the elevation in the synaptic or presynaptic DA concentrations in the schizophrenic brain, based on the hypothesis that any mutation changing the amino acid sequence Gly36-Arg37-Arg38 would result in the elevation of DA synthesis, due to a reduced inhibitory effect of DA on the catalytic activity. However, no mutated sequences of exon 3 and both exon-intron boundaries were detected in any of the patients examined. Polymorphisms generating Val81 and Met81 were compared of the distributions of genotype and allele between the patients and 175 Japanese healthy controls, which did not suggest an association between the polymorphism and schizophrenia. These results indicate that exon 3 of the human TH gene lacks association with schizophrenia in Japanese patients.
AB - Tyrosine hydroxylase (TH) is the rate-limiting enzyme in dopamine (DA) biosynthesis. Exon 3 of the human TH gene encodes the sequence from Set31 to Glu104 of type 1 enzyme, which contains the critical parts for regulation of the catalytic activity. The amino acid residues Gly36-Arg37-Arg38 were identified as a key sequence for DA to exert its inhibitory effect on catalytic activity. Therefore, we screened the nucleotide sequences of exon 3 from 201 Japanese patients with schizophrenia to explain the elevation in the synaptic or presynaptic DA concentrations in the schizophrenic brain, based on the hypothesis that any mutation changing the amino acid sequence Gly36-Arg37-Arg38 would result in the elevation of DA synthesis, due to a reduced inhibitory effect of DA on the catalytic activity. However, no mutated sequences of exon 3 and both exon-intron boundaries were detected in any of the patients examined. Polymorphisms generating Val81 and Met81 were compared of the distributions of genotype and allele between the patients and 175 Japanese healthy controls, which did not suggest an association between the polymorphism and schizophrenia. These results indicate that exon 3 of the human TH gene lacks association with schizophrenia in Japanese patients.
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U2 - 10.1038/sj.mp.4000840
DO - 10.1038/sj.mp.4000840
M3 - Article
C2 - 11326301
AN - SCOPUS:17744397099
SN - 1359-4184
VL - 6
SP - 315
EP - 319
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 3
ER -