2003 Fiscal Year Final Research Report Summary
Identification of genomic regions associated with schizophrenia using exploratory eye movements
| Project/Area Number |
14370295
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Psychiatric science
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| Research Institution | Nihon University |
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Principal Investigator |
KOJIMA Takuya Nihon University, Department of Neuropsychiatry, School of Medicine, Professor, 医学部, 教授 (40014203)
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| Co-Investigator(Kenkyū-buntansha) |
OHKUBO Tatsunobu Nihon University, Department of Neuropsychiatry, School of Medicine, Lecturer, 医学部, 講師 (90328716)
ARINAMI Tadao University Tsukuba, Department of Medical Genetics, Institute of Basic Medical Science, Professor, 基礎医学系, 教授 (10212648)
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| Project Period (FY) |
2002 – 2003
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| Keywords | Schizophrenia / Exploratory Eye / Linkage Analysis / Quantitative Trait Measure / Endophenotype / Endophenotype |
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| Research Abstract |
A biological marker that is related to a genetic predisposition to schizophrenia could lead to identification of a major susceptibility locus for schizophrenic illness. Our previous study of a genome-wide scan for a locus responsible for exploratory eye movement (EEM), which can be disturbed in association with schizophrenia, revealed significant linkage between EEM and 22q. Identifying gene(s) on chromosome 22q associated with the EEM phenotype may forward our understanding of the etiology of schizophrenia. To identify genomic region(s) associated with schizophrenia on 22q, we examined 22q in association with schizophrenia.
A total of 68 families with 274 members were analyzed. At least one schizophrenic patient was included in each family Deletion screening was performed for 1505 unrelated Japanese subjects. Short andem repeat polymorphisms (STRPs) and single nucleotide polymorphisms (SNPs) were detected and genotyped for assessing linkage disequilibrium (LD) blocks. LD blocks were computed by a GOLD program and LD/association with schizophrenia was assessed by transmission disequilibrium test (TDT). In addition to 22q11.2, 22q12.1, and 22q12.3, mutations were screened for four genes of APOL1, APOL2, APOL3, and APOL4 in 22q12.3. The study was approved by the Ethics Committees of Nihon University and University of Tsukuba.
we identified novel STRPs in 22q11.2 region and detected LD blocks associated with schizophrenia. We also found that genomic neighboring regions of the APOL1 and APOL4 geneswere associated with schizophrenia. We clearly demonstrated that deletion of the PRODH gene do not raise a risk of schizophrenia greatly
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Research Products
(19 results)
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[Publications] Takahashi S, Ohtsuki T, Yu SY, Tanabe E, Yara K, Kamioka M, Matsushima E, Matsuura M, Ishikawa K, Minowa Y, Noguchi E, Nakayama J, Yamakawa-Kobayashi K, Arinami T, Kojima T: "Significant Linkage to Chromosome 22q for Exploratory Eye Movement Dysfunction in Schizophre"Am J Med Genet. 123B. 27-32 (2003)
Description
「研究成果報告書概要(欧文)」より
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