Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch

被引:306
作者
Igarashi, S
Koide, R
Shimohata, T
Yamada, M
Hayashi, Y
Takano, H
Date, H
Oyake, M
Sato, T
Sato, A
Egawa, S
Ikeuchi, T
Tanaka, H
Nakano, R
Tanaka, K
Hozumi, I
Inuzuka, T
Takahashi, H
Tsuji, S
机构
[1] Niigata Univ, Brain Res Inst, Dept Neurol, Niigata 951, Japan
[2] Niigata Univ, Brain Res Inst, Dept Pathol, Niigata 951, Japan
关键词
D O I
10.1038/ng0298-111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To elucidate the molecular mechanisms whereby expanded polyglutamine stretches elicit a gain of toxic function, we expressed full-length and truncated DRPLA (dentatorubral-pallidoluysian atrophy) cDNAs with or without expanded CAG repeats in COS-7 cells. We found that truncated DRPLA proteins containing an expanded polyglutamine stretch form filamentous peri-and intranuclear aggregates and undergo apoptosis. The apoptotic cell death was partially suppressed by the transglutaminase inhibitors cystamine and monodansyl cadaverine (but not putrescine), suggesting involvement of a transglutaminase reaction and providing a potential basis for the development of therapeutic measures for GAG-repeat expansion diseases.
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收藏
页码:111 / 117
页数:7
相关论文
共 38 条
[1]   SCA1 TRANSGENIC MICE - A MODEL FOR NEURODEGENERATION CAUSED BY AN EXPANDED CAG TRINUCLEOTIDE REPEAT [J].
BURRIGHT, EN ;
CLARK, HB ;
SERVADIO, A ;
MATILLA, T ;
FEDDERSEN, RM ;
YUNIS, WS ;
DUVICK, LA ;
ZOGHBI, HY ;
ORR, HT .
CELL, 1995, 82 (06) :937-948
[2]   Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion [J].
David, G ;
Abbas, N ;
Stevanin, G ;
Durr, A ;
Yvert, G ;
Cancel, G ;
Weber, C ;
Imbert, G ;
Saudou, F ;
Antoniou, E ;
Drabkin, H ;
Gemmill, R ;
Giunti, P ;
Benomar, A ;
Wood, N ;
Ruberg, M ;
Agid, Y ;
Mandel, JL ;
Brice, A .
NATURE GENETICS, 1997, 17 (01) :65-70
[3]   Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation [J].
Davies, SW ;
Turmaine, M ;
Cozens, BA ;
DiFiglia, M ;
Sharp, AH ;
Ross, CA ;
Scherzinger, E ;
Wanker, EE ;
Mangiarini, L ;
Bates, GP .
CELL, 1997, 90 (03) :537-548
[4]  
DICKSON RB, 1981, J BIOL CHEM, V256, P3454
[5]   Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain [J].
DiFiglia, M ;
Sapp, E ;
Chase, KO ;
Davies, SW ;
Bates, GP ;
Vonsattel, JP ;
Aronin, N .
SCIENCE, 1997, 277 (5334) :1990-1993
[6]   Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract [J].
Goldberg, YP ;
Nicholson, DW ;
Rasper, DM ;
Kalchman, MA ;
Koide, HB ;
Graham, RK ;
Bromm, M ;
KazemiEsfarjani, P ;
Thornberry, NA ;
Vaillancourt, JP ;
Hayden, MR .
NATURE GENETICS, 1996, 13 (04) :442-449
[7]   Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo [J].
Ikeda, H ;
Yamaguchi, M ;
Sugai, S ;
Aze, Y ;
Narumiya, S ;
Kakizuka, A .
NATURE GENETICS, 1996, 13 (02) :196-202
[8]   DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY - CLINICAL-FEATURES ARE CLOSELY-RELATED TO UNSTABLE EXPANSIONS OF TRINUCLEOTIDE (CAG) REPEAT [J].
IKEUCHI, T ;
KOIDE, R ;
TANAKA, H ;
ONODERA, O ;
IGARASHI, S ;
TAKAHASHI, H ;
KONDO, R ;
ISHIKAWA, A ;
TOMODA, A ;
MIIKE, T ;
SATO, K ;
IHARA, Y ;
HAYABARA, T ;
ISA, F ;
TANABE, H ;
TOKIGUCHI, S ;
HAYASHI, M ;
SHIMIZU, N ;
IKUTA, F ;
NAITO, H ;
TSUJI, S .
ANNALS OF NEUROLOGY, 1995, 37 (06) :769-775
[9]   Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats [J].
Imbert, G ;
Saudou, F ;
Yvert, G ;
Devys, D ;
Trottier, Y ;
Garnier, JM ;
Weber, C ;
Mandel, JL ;
Cancel, G ;
Abbas, N ;
Durr, A ;
Didierjean, O ;
Stevanin, G ;
Agid, Y ;
Brice, A .
NATURE GENETICS, 1996, 14 (03) :285-291
[10]   THE CORTICAL NEURITIC PATHOLOGY OF HUNTINGTONS-DISEASE [J].
JACKSON, M ;
GENTLEMAN, S ;
LENNOX, G ;
WARD, L ;
GRAY, T ;
RANDALL, K ;
MORRELL, K ;
LOWE, J .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1995, 21 (01) :18-26