Human Molecular Genetics, 2000, Vol. 9, No. 13 2009-2018
© 2000 Oxford University Press
Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity
Laboratory for CAG Repeat Diseases, RIKEN Brain Science Institute, 21 Hirosawa, Wako-shi, Saitama 351-0198, Japan
Huntingtons disease (HD) is an autosomal dominant neurodegenerative disorder caused by polyglutamine expansion in the disease protein, huntingtin. In HD patients and transgenic mice, the affected neurons form characteristic ubiquitin-positive nuclear inclusions (NIs). We have established ecdysone-inducible stable mouse Neuro2a cell lines that express truncated N-terminal huntingtin (tNhtt) with different polyglutamine lengths which form both cytoplasmic and nuclear aggregates in a polyglutamine length- and inducer dose-dependent manner. Here we demonstrate that newly synthesized polyglutamine-expanded truncated huntingtin interacts with members of Hsp40 and Hsp70 families of chaperones in a polyglutamine length-dependent manner. Of these interacting chaperones, only Hdj-2 and Hsc70 frequently (Hdj-2 > Hsc70) co-localize with both the aggregates in the cellular model and with the NIs in the brains of HD exon 1 transgenic mice. However, Hdj-2 and Hsc70 do not co-localize with cytoplasmic aggregates in the brains of transgenic mice despite these chaperones being primarily localized in the cytoplasmic compartment. This strongly suggests that the chaperone interaction and their redistribution to the aggregates are two completely different phenomena of the cellular unfolded protein response. This unfolded protein response is also evident from the dramatic induction of Hsp70 on expression of polyglutamine-expanded protein in the cellular model. Transient overexpression of either Hdj-1 or Hsc70 suppresses the aggregate formation; however, suppression efficiency is much higher in Hdj-1 compared with Hsc70. Overexpression of Hdj-1 and Hsc70 is also able to protect cell death caused by polyglutamine-expanded tNhtt and their combination proved to be most effective.
+ To whom correspondence should be addressed. Tel: +81 48 467 9702; Fax: +81 48 462 4796; Email: nukina@brain.riken.go.jp
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||||
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||||
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||||
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||||
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||||
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||||
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||||
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||||
![]() |
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||||
![]() |
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||||
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||||
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K. Mitsui, H. Nakayama, T. Akagi, M. Nekooki, K. Ohtawa, K. Takio, T. Hashikawa, and N. Nukina Purification of Polyglutamine Aggregates and Identification of Elongation Factor-1alpha and Heat Shock Protein 84 as Aggregate-Interacting Proteins J. Neurosci., November 1, 2002; 22(21): 9267 - 9277. [Abstract] [Full Text] [PDF] |
||||
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V. Fonte, V. Kapulkin, A. Taft, A. Fluet, D. Friedman, and C. D. Link Interaction of intracellular beta amyloid peptide with chaperone proteins PNAS, July 9, 2002; 99(14): 9439 - 9444. [Abstract] [Full Text] [PDF] |
||||
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Y. Kouroku, E. Fujita, A. Jimbo, T. Kikuchi, T. Yamagata, M. Y. Momoi, E. Kominami, K. Kuida, K. Sakamaki, S. Yonehara, et al. Polyglutamine aggregates stimulate ER stress signals and caspase-12 activation Hum. Mol. Genet., June 15, 2002; 11(13): 1505 - 1515. [Abstract] [Full Text] [PDF] |
||||
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||||
![]() |
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||||
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||||
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||||
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||||
![]() |
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||||
![]() |
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||||
![]() |
S Lovestone and D M McLoughlin Protein aggregates and dementia: is there a common toxicity? J. Neurol. Neurosurg. Psychiatry, February 1, 2002; 72(2): 152 - 161. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Zhou, S.-H. Li, and X.-J. Li Chaperone Suppression of Cellular Toxicity of Huntingtin Is Independent of Polyglutamine Aggregation J. Biol. Chem., December 14, 2001; 276(51): 48417 - 48424. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. J. Welch and M. I. Diamond Glucocorticoid modulation of androgen receptor nuclear aggregation and cellular toxicity is associated with distinct forms of soluble expanded polyglutamine protein Hum. Mol. Genet., December 1, 2001; 10(26): 3063 - 3074. [Abstract] [Full Text] [PDF] |
||||
![]() |
S Davies and D B Ramsden Huntington's disease Mol. Pathol., December 1, 2001; 54(6): 409 - 413. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Sathasivam, B. Woodman, A. Mahal, F. Bertaux, E. E. Wanker, D. T. Shima, and G. P. Bates Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients Hum. Mol. Genet., October 1, 2001; 10(21): 2425 - 2435. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Wyttenbach, J. Swartz, H. Kita, T. Thykjaer, J. Carmichael, J. Bradley, R. Brown, M. Maxwell, A. Schapira, T. F. Orntoft, et al. Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington's disease Hum. Mol. Genet., August 1, 2001; 10(17): 1829 - 1845. [Abstract] [Full Text] [PDF] |
||||
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||||
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