2006 Fiscal Year Final Research Report Summary
The analysis of Familial Parkinson's disease gene products and the research for identification of a novel Familial Parkinson's disease gene
Project/Area Number |
17390256
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Neurology
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Research Institution | JUNTENDO UNIVERSITY |
Principal Investigator |
HATTORI Nobutaka Juntendo Medical, Professor, 医学部, 教授 (80218510)
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Co-Investigator(Kenkyū-buntansha) |
SATO Kenichi Juntendo Medical, Associate Professor, 医学部, 准教授 (00276461)
KUBO Shin-ichiro Juntendo Medical, Associate Professor, 医学部, 准教授 (20327795)
HIRASAWA Motoyuki Juntendo Medical, Associate Professor, 医学部, 准教授 (90338393)
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Project Period (FY) |
2005 – 2006
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Keywords | Parkinson's disease / Familial Parkinson's disease / ubiquitin-proteasome / 24-kDa subunit / mitochondrial dysfunction / PINK1 / DJ-1 / Knock-out mice |
Research Abstract |
Parkinson's disease (PD) is the second most common neurodegenerative disorder with a prevalence of 1% in individuals older than 65 years of age. Although the majority of PD cases are sporadic, it is now clear that genetic factors contribute to the pathogenesis of PD. Until now, seven causative genes for familial PD (FPD) have been identified. Considering the clinical phenotypes such as parkinsonism, it would be possible that FPD gene products share a common pathway. As parkin is direct linked to ubiquitin-pathway as an E3, this product is also thought to function for mitochondria. PINK1 and DJ-1 are also associated with mitochondria. Thus, mitochondrion is a target organella for elucidating the pathogenesis of FPD. In the present study, we found a common pathway between α-synuclein, parkin, PINK1, and DJ-1. In contrast, half of the autosomal recessive FPD showed no mutations in the known causative genes Therefore, we continue to perform the linkage study for identification of a novel gene. On the mapping for a causative gene responsible for late onset PD with autosomal recessive mode of inheritance, a few loci for this form of PD could be identified.
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Research Products
(30 results)
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[Journal Article] Sept4, a Component of Presynaptic Scaffold and Lewy Bodies, Is Required for the Suppression of alpha-Synuclein Neurotoxicity.2007
Author(s)
Ihara M, Yamasaki N, Hagiwara A, Tanigaki A, Kitano A, Hikawa R, Tomimoto H, Noda M, Takanashi M, Mori H, Hattori N, Miyakawa T, Kinoshita M.
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Journal Title
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.2007
Author(s)
Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari PA, Leppert D, Surh L, Reeves KH, Thomas S, Ragone L, Hattori N, Pahwa R, Jankovic J, Nance M, Freeman A, Gouider-Khouja N, Kefi M, Zouari M, Ben Sassi S, Ben Yahmed S, El Euch-Fayeche G, Middleton L, Burn DJ, Watts RL, Hentati F
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Journal Title
Mov Disord 22
Pages: 55-61
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier2007
Author(s)
Kono S, Shirakawa K, Ouchi Y, Sakamoto M, Ida H, Sugiura T, Tomiyama H, Suzuki H, Takahashi Y, Miyajima H, Hattori N, Mizuno Y.
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Journal Title
J Neurol Sci 252
Pages: 181-184
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Parkinson's disease : a hint to elucidate the mechanisms of nigral degeneration.2007
Author(s)
Ihara M, Yamasaki N, Hagiwara A, Tanigaki A, Kitano A, Hikawa R, Tomimoto H, Noda M, Takanashi M, Mori H, Hattori N, Miyakawa T, Kinoshita M, Familial
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Journal Title
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families2007
Author(s)
Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari PA, Leppert D, Surh L, Reeves KH, Thomas S, Ragone L, Hattori N, Pahwa R, Jankovic J, Nance M, Freeman A, Gouider-Khouja N, Kefi M, Zouari M, Ben Sassi S, Ben Yahmed S, El Euch-Fayeche G, Middleton L, Burn DJ, Watts RL, Hentati F
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Journal Title
Mov Disord 22
Pages: 55-61
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Decline of striatal dopamine release in parkin-deficient mice shown by ex vivo autoradiography2007
Author(s)
Sato S, Chiba T, Nishiyama S, Kakiuchi T, Tsukada H, Hatano T, Fukuda T, Yasoshima Y, Kai N, Kobayashi K, Mizuno Y, Tanaka K, Hattori N
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Journal Title
J Neurosci Res 84
Pages: 1350-1357
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Prognosis of Parkinson's disease : time to stage III, IV, V, and to motor fluctuations2007
Author(s)
Sato K, Hatano T, Yamashiro K, Kagohashi M, Nishioka K, Izawa N, Mochizuki H, Hattori N, Mori H, Mizuno Y
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Journal Title
Mov Disord 21
Pages: 1384-1395
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier2007
Author(s)
Kono S, Shirakawa K, Ouchi Y, Sakamoto M, Ida H, Sugiura T, Tomiyama H, Suzuki H, Takahashi Y, Miyajima H, Hattori N, Mizuno Y
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Journal Title
J Neurol Sci 252
Pages: 181-184
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Prognosis of Parkinson's disease : time to stage III, IV, V, and to motor fluctuations.2006
Author(s)
Sato K, Hatano T, Yamashiro K, Kagohashi M, Nishioka K, Izawa N, Mochizuki H, Hattori N, Mori H, Mizuno Y
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Journal Title
Mov Disord 21
Pages: 1384-1395
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Decline of striatal dopamine release in parkin-deficient mice shown by ex vivo autoradiography2006
Author(s)
Sato S, Chiba T, Nishiyama S, Kakiuchi T, Tsukada H, Hatano T, Fukuda T, YasoshimaY, Kai N, Kobayashi K, Mizuno Y, Tanaka K, Hattori N
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Journal Title
J Neurosci Res 84
Pages: 1350-1357
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Bispecific antibodies against modified protein and DNA with oxidized lipids2006
Author(s)
Akagawa M, Ito S, Toyoda K, Ishii Y, Tatsuda E, Shibata T, Kawai Y, Ishino K, Kishi Y, Adachi T, Tsubata T, Takasaki Y, Hattori N, Matsuda T, Uchida K
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Journal Title
Proc Natl Acad Sci USA 103
Pages: 6160-6165
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries2006
Author(s)
Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu C-S, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N
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Journal Title
Mov Disord 21
Pages: 1102-1108
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease2006
Author(s)
Nishioka K, Hayashi S, Farrer MJ, Singleton AB, Yoshino H, Imai H, Kitami T, Sato K, Kuroda R, Tomiyama H, Mizoguchi K, Murata M, Toda T, Imoto I, Inazawa J, Mizuno Y, Hattori N
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Journal Title
Ann Neurol 59
Pages: 298-309
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease2006
Author(s)
Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T
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Journal Title
Hum Mol Genet 15
Pages: 1151-1158
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Clinical features of Parkinson's patients with and without LRRK2 mutations2006
Author(s)
Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari A, Leppert D, Surh L, Reeves KH, Thomas S, Ragone L, Hattori N, Pahwa R, Jankovic J, Nance M, Freeman A, Gouider-Khouja N, Kefi M, Bouar M, Sassi SB, Yahmed SB, Euch-Fayeche EG, Middleton L, Burn DJ, Watts RL, I Hentati F
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Journal Title
Arch Neurol 63
Pages: 1250-1254
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease2006
Author(s)
Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Kruger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G, Hattori N, Kawakami H, Lambert JC, Lynch T, Mellick GD, Papapetropoulos S, Parsian A, Quattrone A, Riess O, Tan EK, Van Broeckhoven C
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Journal Title
Description
「研究成果報告書概要(和文)」より
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[Journal Article] Clinical features of Parkinson's patients with and without LRRK2 mutations2006
Author(s)
Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari A, Leppert D, Surh L, Reeves KH, Thomas S, Ragone L, Hattori N, Pahwa R, Jankovic J, Nance M, Freeman A, Gouider-Khouja N, Kefi M, Bouar M, Sassi SB, Yahmed SB, Euch-Fayeche EG, Middleton L, Burn DJ, Watts RL, 1 Hentati F
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Journal Title
Arch Neurol 63
Pages: 1250-1254
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Van Broeckhoven C, Collaborative analysis of alnha-synuclein gene promoter variability and Parkinson disease2006
Author(s)
Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Kruger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, Ferrarese C, Hadjigeorgiou G Hattori N, Kawakami H, Lambert JC, Lynch T, Mellick GD, Papapetropoulos S, Parsian A, Quattrone A, Riess O, Tan EK
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Journal Title
Description
「研究成果報告書概要(欧文)」より
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