| Project/Area Number |
12670967
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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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 | RIKEN |
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Principal Investigator |
EBIHARA Mitsuru Riken, Laboratory for molecular psychiatry, Researcher, 分子精神科学研究チーム, 研究員 (80232974)
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| Co-Investigator(Kenkyū-buntansha) |
OHBA Hisako Riken, Laboratory for molecular psychiatry, Technical stuff, 分子精神科学研究チーム, テクニカルスタッフ(研究職)
YOSHIKAWA Takeo Riken, Laboratory for molecular psychiatry, Team Leader, 分子精神科学研究チーム, チームリーダー(研究職) (30249958)
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| Project Period (FY) |
2000 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2001: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 2000: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | Epilepsy / BAFME / Potassium channel / Channelopathy / Whole genome scan / Linkage analysis / channellopathy / FEME / FAME |
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| Research Abstract |
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant idiopathic epilepsy characterized by adult-onset, high penetration rate, myoclonus, tremulous finger movement and infrequent epileptic seizure. BAFME was recognized only in Japan.
Linkage analysis was carried out in a Japanese family using ABI Linkage Map Set. Chyomosome 2, 7, 8, 10 and 17 were not excluded by linkage analysis, but it was strongly suggested that BAFME susceptibility locus is within 4.4cM on the human chromosome 8q23-24 by using extra markers. We have isolated more than 40 BAC clones covering one third of BAFME susceptibility region. We also had YAC contig spanning this region. By using these BAC and YAC clones, exon trapping was performed, resulted in the isolation of two novel exonic sequences. The isolation of the longest cDNAS clone from cDNA library revealed that they have neither homology with the other gene, nor ORF in their sequences. We are still going to isolate more 5' region of these clones, containing ORF. We also found three different potassium channel genes (KCNQ3, Kv8.I and Kv9.2) on 8q23-24.Because epilepsies are thought to be channelopathy, these are candidate genes for BAFME. Mutation search was performed on these three potassium channel genes in a Japanese family. We couldn't find any mutation both in the KCNQ3 and Kv8.I gene, but we found an extra 5' exon and possible alternative 3' end in the Kv8.I gene. No mutation was found in the Kv9.2 gene either. Mutation search in the promoter region of these three potassium channel gene are in progress. The possibility of founder effect in Japanese families is also excluded by genotyping of the other families with BAFME.
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