Research for development of therapy of Machado-Joseph disease by siRNA
| Project/Area Number |
15590880
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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 |
Neurology
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| Research Institution | The University of Tokyo |
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Principal Investigator |
GOTO Jun The University of Tokyo, Faculty of Medicine, Lecturer, 医学部附属病院, 講師 (10211252)
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2005: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2004: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2003: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | Machado-Joseph disease / CAG repeat / Polyglutamine / siRNA / Huntington's disease |
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| Research Abstract |
Machado-Joseph disease is a progressive heredodegenerative disease that is caused by unstable expansions of CAG repeats in MJD which is located at chromosome 14q32.1. The mutant ataxin-3, the gene product of MJD, carrying the expanded polyglutamine stretch gains an adverse function and causes dysfunction of neurons, leading to neuronal death. No effective therapeutics has been established. If the expression of the mutant protein could be inhibited, we could treat the disease very well. Short interfering RNA (siRNA) would be a good candidate to establish an effective therapeutics.
Huntington's disease is also one of the polyglutamine diseases and cased by an abnormally expanded CAG repeats in exon 1 of the HD gene. It was investigated that the effects of siRNAs directed against the HD gene in order to knock down its expression in cultured cells. One siRNA, named as siRNA-HD-Exon1, which is targeted against the region at immediate upstream of the CAG repeats, can efficiently and specifically inhibit the expression of HD exon 1-EGFP fusion mini-gene. It also did efficiently suppress the endogenous huntingtin expression in cultured cell lines derived from human neuroblastoma (Proc Japan Acad 79(Ser B) : 293-298, 2003).
There are several single nucleotide polymorphisms (SNPs) in the MJD gene. In Japanese population, there are two haplotypes of those SNPs. One is c527T-c669A-c987C-c1118A and the other is c527C-c669G-c987G-c1118C.Disease chromosomes which carry the abnormally expanded CAG repeats show exclusively the former haplotype. If the expression of the allele carrying that haplotype could be specifically and effectively inhibited by a suitable siRNA, it would be the first step toward the development of a radical therapy for MJD. Two research groups reported successful suppression of the haplotype-specific expression by the siRNA of which the target is the sequence surrounding c987C/G SNP.
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Report
(4 results)
Research Products
(18 results)
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[Journal Article] Japanese SCA families with an autosomal phenotype linked toa locus overlapping with SCA15 locus.2004
Author(s)
Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S
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Journal Title
Neurology 62
Pages: 648-651
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Journal Article] Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan2003
Author(s)
Li M, Ishikawa K, Toru S, Tomimitsu H, Takashiam M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H
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Journal Title
Jornal of Human Genetics 48
Pages: 111-118
NAID
Description
「研究成果報告書概要(欧文)」より
Related Report
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