| Project/Area Number |
09470206
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Psychiatric science
|
|---|
| Research Institution | Hirosaki University |
|---|
Principal Investigator |
KANEKO Sunao Hirosaki University, School of Medicine, Neuropsychiatry, Professor, 医学部, 教授 (40106852)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
SANO Akira Ehime University, School of Medicine, Department Neuropsychiatry, Assistant-professor, 医学部・付属病院, 助教授 (30178800)
NAKAMURA Yusuke University of Tokyo, Institute of Medical Science, Professor, 医科学研究所・ヒトゲノム解析センター, 教授 (70217909)
TSUJI Shoji Niigata University, Brain Research Institute, Department of Neurology, Professor, 脳研究所, 教授 (70150612)
ONUMA Teiichi National Saigata Hospital, Department of Psychiatry, Director, 院長 (30003536)
MITSUNOME Akihisa Fukuoka University, School of Medicine, Department of Pediatrics, Professor, 医学部, 教授 (30038749)
小国 弘量 東京女子医科大学, 助教授 (60130241)
磯村 実 東京大学, がん化学療法センター・ゲノム解析研究部, 助手 (40272497)
|
|---|
| Project Period (FY) |
1997 – 1999
|
| Project Status |
Completed (Fiscal Year 1999)
|
| Budget Amount *help |
¥13,000,000 (Direct Cost: ¥13,000,000)
Fiscal Year 1999: ¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 1998: ¥4,400,000 (Direct Cost: ¥4,400,000)
Fiscal Year 1997: ¥5,000,000 (Direct Cost: ¥5,000,000)
|
|---|
| Keywords | Epilepsy / Epilepsy genes / autosomal dominant nocturnal frontal lobe epilepsy / benign familial neonatal convulsions / benign adult familial myoclonic epilepsy / ion channel |
|---|
| Research Abstract |
Epilepsy is a neurolagical disorder characterized by recurring seizures. Epilepsy affects more than 0.5% of the world's population and has a large genetic component. The most common human genetic epilepsies display a complex pattern of inheritance and the identity of the susceptibility genes is largely unknown.
This report summarizes our own discovery of two novel mutations in the genes of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) and benign familial neonatal convulsions (BFNC), and our mapping of the genetic locus of benign adult familial myoclonic epilepsy (BAFME). A ""C"" to ""T"" exchange (C752T)was found in exon 5 of the CHRNA4 gene on one allele of individuals with ADNFLE. C752T replaced SerィイD1252ィエD1 in the second membrane spanning domain (M2) of CHRNA4 with a leucine. SerィイD1252ィエD1 is conserved characteristically in the α4 subunit acetylcholine recepter, a α4 subunit acetylcholine receptor that is considered to play an important role in the channel function. We screened six Japanese families with BFNC for mutations of KCNQ3, and found a T to C exchange (cDNA925T> on one allele in affected individuals in a family but not on 200 alleles of healthy volunteers. cDNA925T>C replaced Try262, a conserved residue within P-loop of the KCNQ family, with an Arg (W262R). The gene for BAPME was assigned to chromosome 8q23.3-q24.1 in a Japanese family by this study.
The present results support a hypothesis that some types of idiopathic epilepsy are a form of channelopathy.
Understanding gained from work in this areas of epilepsy research is not only allowing characterization of the molecular and physiologic basis of these epilepsies, but also ultimately sheds light on our understanding of pathophysiology of more common epilepsies, and promises new vistas of AED and may benefit large numbers of affected individuals.
|
