Human Molecular Genetics, 2000, Vol. 9, No. 1 13-25
© 2000 Oxford University Press
Expanded polyglutamine peptides alone are intrinsically cytotoxic and cause neurodegeneration in Drosophila
Developmental Biology Center and Department of Developmental and Cell Biology, and 1Department of Biological Chemistry, D240 Medical Sciences I, University of CaliforniaIrvine, Irvine, CA 92697-1700, USA
Several dominant, late-onset neurodegenerative diseases (e.g. Huntingtons disease) are caused by expansion of polyglutamine (polyQ) repeats within specific proteins. The diverse, yet overlapping, pathology of these diseases could be due to novel deleterious functions unique to each protein or to a common pathophysiology mediated by the long polyQ chains themselves. By engineering Drosophila to express different polyQ peptides, we find that expanded polyQ chains alone are intrinsically cytotoxic and cause neuronal degeneration and early adult death. We further find that this intrinsic toxicity is dependent on cell type and polyQ length and that the inclusion of other amino acids modifies and reduces toxicity. This is the first in vivo evidence that polyQs, when removed from their disease gene context, cause neurotoxicity. These studies provide a basis for understanding the diverse clinical presentations in terms of the intrinsic cytotoxic effect of polyQ peptides being modulated by protein context. Parallel experiments in which cytotoxic polyQ expansions were engineered into Dishevelled, a Drosophila protein containing a naturally occurring polyQ tract, strongly suggest that the effect of a toxic polyQ peptide can be neutralized by protein context. This animal model provides a simple and effective means of screening for therapeutics that relieves the polyQ-induced lethality, independent of any particular disease gene. By quantifying the degree of lethality in several transgenic lines, we have identified a number of genetically modified strains that are suitable for eventual testing of compounds or genes that ameliorate the pathology of polyQ peptides.
+ Present address: Department of Biological Science, California State UniversityFullerton, PO Box 6080, Fullerton, CA 92834-6080, USA
§ To whom correspondence should be addressed. Tel: +1 949 824 6756; Fax: +1 949 824 2688; Email: lmthomps@uci.edu
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
K. Venderova, G. Kabbach, E. Abdel-Messih, Y. Zhang, R. J. Parks, Y. Imai, S. Gehrke, J. Ngsee, M. J. LaVoie, R. S. Slack, et al. Leucine-rich repeat kinase 2 interacts with Parkin, DJ-1 and PINK-1 in a Drosophila melanogaster model of Parkinson's disease Hum. Mol. Genet., November 15, 2009; 18(22): 4390 - 4404. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. T. Aiken, J. S. Steffan, C. M. Guerrero, H. Khashwji, T. Lukacsovich, D. Simmons, J. M. Purcell, K. Menhaji, Y.-Z. Zhu, K. Green, et al. Phosphorylation of Threonine 3: IMPLICATIONS FOR HUNTINGTIN AGGREGATION AND NEUROTOXICITY J. Biol. Chem., October 23, 2009; 284(43): 29427 - 29436. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Raspe, J. Gillis, H. Krol, S. Krom, K. Bosch, H. van Veen, and E. Reits Mimicking proteasomal release of polyglutamine peptides initiates aggregation and toxicity J. Cell Sci., September 15, 2009; 122(18): 3262 - 3271. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Mugat, M.-L. Parmentier, N. Bonneaud, H. Y. E. Chan, and F. Maschat Protective role of Engrailed in a Drosophila model of Huntington's disease Hum. Mol. Genet., November 15, 2008; 17(22): 3601 - 3616. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Southwell, A. Khoshnan, D. E. Dunn, C. W. Bugg, D. C. Lo, and P. H. Patterson Intrabodies Binding the Proline-Rich Domains of Mutant Huntingtin Increase Its Turnover and Reduce Neurotoxicity J. Neurosci., September 3, 2008; 28(36): 9013 - 9020. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. I. Morimoto Proteotoxic stress and inducible chaperone networks in neurodegenerative disease and aging Genes & Dev., June 1, 2008; 22(11): 1427 - 1438. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-C. Lievens, M. Iche, M. Laval, C. Faivre-Sarrailh, and S. Birman AKT-sensitive or insensitive pathways of toxicity in glial cells and neurons in Drosophila models of Huntington's disease Hum. Mol. Genet., March 15, 2008; 17(6): 882 - 894. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Scappini, T.-W. Koh, N. P. Martin, and J. P. O'Bryan Intersectin enhances huntingtin aggregation and neurodegeneration through activation of c-Jun-NH2-terminal kinase Hum. Mol. Genet., August 1, 2007; 16(15): 1862 - 1871. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Latouche, C. Lasbleiz, E. Martin, V. Monnier, T. Debeir, A. Mouatt-Prigent, M.-P. Muriel, L. Morel, M. Ruberg, A. Brice, et al. A Conditional Pan-Neuronal Drosophila Model of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes J. Neurosci., March 7, 2007; 27(10): 2483 - 2492. [Abstract] [Full Text] [PDF] |
||||
![]() |
T.-K. Sang, H.-Y. Chang, G. M. Lawless, A. Ratnaparkhi, L. Mee, L. C. Ackerson, N. T. Maidment, D. E. Krantz, and G. R. Jackson A Drosophila Model of Mutant Human Parkin-Induced Toxicity Demonstrates Selective Loss of Dopaminergic Neurons and Dependence on Cellular Dopamine J. Neurosci., January 31, 2007; 27(5): 981 - 992. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. A. Gavin, M. J. Dolph, N. R. Deleault, J. C. Geoghegan, V. Khurana, M. B. Feany, P. J. Dolph, and S. Supattapone Accelerated Accumulation of Misfolded Prion Protein and Spongiform Degeneration in a Drosophila Model of Gerstmann-Straussler-Scheinker Syndrome J. Neurosci., November 29, 2006; 26(48): 12408 - 12414. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Berger, B. Ravikumar, F. M. Menzies, L. G. Oroz, B. R. Underwood, M. N. Pangalos, I. Schmitt, U. Wullner, B. O. Evert, C. J. O'Kane, et al. Rapamycin alleviates toxicity of different aggregate-prone proteins Hum. Mol. Genet., February 1, 2006; 15(3): 433 - 442. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Delalle, C. M. Pfleger, E. Buff, P. Lueras, and I. K. Hariharan Mutations in the Drosophila Orthologs of the F-Actin Capping Protein {alpha}- and {beta}-Subunits Cause Actin Accumulation and Subsequent Retinal Degeneration Genetics, December 1, 2005; 171(4): 1757 - 1765. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Berger, E. K. Ttofi, C. H. Michel, M. Y. Pasco, S. Tenant, D. C. Rubinsztein, and C. J. O'Kane Lithium rescues toxicity of aggregate-prone proteins in Drosophila by perturbing Wnt pathway Hum. Mol. Genet., October 15, 2005; 14(20): 3003 - 3011. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. L. Benn, C. Landles, H. Li, A. D. Strand, B. Woodman, K. Sathasivam, S.-H. Li, S. Ghazi-Noori, E. Hockly, S. M.N.N. Faruque, et al. Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease Hum. Mol. Genet., October 15, 2005; 14(20): 3065 - 3078. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Celotto and M. J. Palladino Drosophila: A "Model" Model System To Study Neurodegeneration Mol. Interv., October 1, 2005; 5(5): 292 - 303. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. J. Wolfgang, T. W. Miller, J. M. Webster, J. S. Huston, L. M. Thompson, J. L. Marsh, and A. Messer Suppression of Huntington's disease pathology in Drosophila by human single-chain Fv antibodies PNAS, August 9, 2005; 102(32): 11563 - 11568. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Iijima-Ando, P. Wu, E. A. Drier, K. Iijima, and J. C. P. Yin cAMP-response element-binding protein and heat-shock protein 70 additively suppress polyglutamine-mediated toxicity in Drosophila PNAS, July 19, 2005; 102(29): 10261 - 10266. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. J. McLeod, L. V. O'Keefe, and R. I. Richards The pathogenic agent in Drosophila models of 'polyglutamine' diseases Hum. Mol. Genet., April 15, 2005; 14(8): 1041 - 1048. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-C. Lievens, T. Rival, M. Iche, H. Chneiweiss, and S. Birman Expanded polyglutamine peptides disrupt EGF receptor signaling and glutamate transporter expression in Drosophila Hum. Mol. Genet., March 1, 2005; 14(5): 713 - 724. [Abstract] [Full Text] [PDF] |
||||
![]() |
T.-K. Sang, C. Li, W. Liu, A. Rodriguez, J. M. Abrams, S. L. Zipursky, and G. R. Jackson Inactivation of Drosophila Apaf-1 related killer suppresses formation of polyglutamine aggregates and blocks polyglutamine pathogenesis Hum. Mol. Genet., February 1, 2005; 14(3): 357 - 372. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Zhang, D. L. Smith, A. B. Meriin, S. Engemann, D. E. Russel, M. Roark, S. L. Washington, M. M. Maxwell, J. L. Marsh, L. M. Thompson, et al. A potent small molecule inhibits polyglutamine aggregation in Huntington's disease neurons and suppresses neurodegeneration in vivo PNAS, January 18, 2005; 102(3): 892 - 897. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. D. Buckingham, B. Esmaeili, M. Wood, and D. B. Sattelle RNA interference: from model organisms towards therapy for neural and neuromuscular disorders Hum. Mol. Genet., October 1, 2004; 13(suppl_2): R275 - R288. [Abstract] [Full Text] [PDF] |
||||
![]() |
X.-C. Zeng, S. Bhasin, X. Wu, J.-G. Lee, S. Maffi, C. J. Nichols, K. J. Lee, J. P. Taylor, L. E. Greene, and E. Eisenberg Hsp70 dynamics in vivo: effect of heat shock and protein aggregation J. Cell Sci., October 1, 2004; 117(21): 4991 - 5000. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-C. M. Lee, M. Yoshihara, and J. T. Littleton Cytoplasmic aggregates trap polyglutamine-containing proteins and block axonal transport in a Drosophila model of Huntington's disease PNAS, March 2, 2004; 101(9): 3224 - 3229. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Michalik and C. Van Broeckhoven Pathogenesis of polyglutamine disorders: aggregation revisited Hum. Mol. Genet., October 15, 2003; 12(90002): R173 - 186. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Marsh, J. Pallos, and L. M. Thompson Fly models of Huntington's disease Hum. Mol. Genet., October 15, 2003; 12(90002): R187 - 193. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Trushina, M. P. Heldebrant, C. M. Perez-Terzic, R. Bortolon, I. V. Kovtun, J. D. Badger II, A. Terzic, A. Estevez, A. J. Windebank, R. B. Dyer, et al. Microtubule destabilization and nuclear entry are sequential steps leading to toxicity in Huntington's disease PNAS, October 14, 2003; 100(21): 12171 - 12176. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. C. Tsai, P. S. Fishman, N. V. Thakor, and G. A. Oyler Parkin Facilitates the Elimination of Expanded Polyglutamine Proteins and Leads to Preservation of Proteasome Function J. Biol. Chem., June 6, 2003; 278(24): 22044 - 22055. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. L. Apostol, A. Kazantsev, S. Raffioni, K. Illes, J. Pallos, L. Bodai, N. Slepko, J. E. Bear, F. B. Gertler, S. Hersch, et al. A cell-based assay for aggregation inhibitors as therapeutics of polyglutamine-repeat disease and validation in Drosophila PNAS, May 13, 2003; 100(10): 5950 - 5955. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. D. Finley, P. T. Edeen, R. C. Cumming, M. D. Mardahl-Dumesnil, B. J. Taylor, M. H. Rodriguez, C. E. Hwang, M. Benedetti, and M. McKeown blue cheese Mutations Define a Novel, Conserved Gene Involved in Progressive Neural Degeneration J. Neurosci., February 15, 2003; 23(4): 1254 - 1264. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Ross, M. A. Poirier, E. E. Wanker, and M. Amzel Polyglutamine fibrillogenesis: The pathway unfolds PNAS, January 7, 2003; 100(1): 1 - 3. [Full Text] [PDF] |
||||
![]() |
P. W. Faber, C. Voisine, D. C. King, E. A. Bates, and A. C. Hart Glutamine/proline-rich PQE-1 proteins protect Caenorhabditis elegans neurons from huntingtin polyglutamine neurotoxicity PNAS, December 24, 2002; 99(26): 17131 - 17136. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Kazemi-Esfarjani and S. Benzer Suppression of polyglutamine toxicity by a Drosophila homolog of myeloid leukemia factor 1 Hum. Mol. Genet., October 2, 2002; 11(21): 2657 - 2672. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. F. Morley, H. R. Brignull, J. J. Weyers, and R. I. Morimoto The threshold for polyglutamine-expansion protein aggregation and cellular toxicity is dynamic and influenced by aging in Caenorhabditiselegans PNAS, August 6, 2002; 99(16): 10417 - 10422. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Wyttenbach, O. Sauvageot, J. Carmichael, C. Diaz-Latoud, A.-P. Arrigo, and D. C. Rubinsztein Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtin Hum. Mol. Genet., May 1, 2002; 11(9): 1137 - 1151. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Khoshnan, J. Ko, and P. H. Patterson Effects of intracellular expression of anti-huntingtin antibodies of various specificities on mutant huntingtin aggregation and toxicity PNAS, January 22, 2002; 99(2): 1002 - 1007. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. J. Caplen, J. P. Taylor, V. S. Statham, F. Tanaka, A. Fire, and R. A. Morgan Rescue of polyglutamine-mediated cytotoxicity by double-stranded RNA-mediated RNA interference Hum. Mol. Genet., January 1, 2002; 11(2): 175 - 184. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. I. Richards Dynamic mutations: a decade of unstable expanded repeats in human genetic disease Hum. Mol. Genet., October 1, 2001; 10(20): 2187 - 2194. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Adachi, A. Kume, M. Li, Y. Nakagomi, H. Niwa, J. Do, C. Sang, Y. Kobayashi, M. Doyu, and G. Sobue Transgenic mice with an expanded CAG repeat controlled by the human AR promoter show polyglutamine nuclear inclusions and neuronal dysfunction without neuronal cell death Hum. Mol. Genet., May 1, 2001; 10(10): 1039 - 1048. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Kazemi-Esfarjani and S. Benzer Genetic Suppression of Polyglutamine Toxicity in Drosophila Science, March 10, 2000; 287(5459): 1837 - 1840. [Abstract] [Full Text] |
||||
![]() |
A. Khoshnan, J. Ko, and P. H. Patterson Effects of intracellular expression of anti-huntingtin antibodies of various specificities on mutant huntingtin aggregation and toxicity PNAS, January 22, 2002; 99(2): 1002 - 1007. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. E. Hughes, R. S. Lo, C. Davis, A. D. Strand, C. L. Neal, J. M. Olson, and S. Fields Altered transcription in yeast expressing expanded polyglutamine PNAS, November 6, 2001; 98(23): 13201 - 13206. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Parker, J. B. Connolly, C. Wellington, M. Hayden, J. Dausset, and C. Neri Expanded polyglutamines in Caenorhabditis elegans cause axonal abnormalities and severe dysfunction of PLM mechanosensory neurons without cell death PNAS, November 6, 2001; 98(23): 13318 - 13323. [Abstract] [Full Text] [PDF] |
||||








