Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70. (Q52574703)

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2 November 2019

title

Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70 (English)

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2 November 2019

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1 reference

2

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2 November 2019

author name string

J M Warrick

1

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2 November 2019

G L Gray-Board

3

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2 November 2019

Y Chai

4

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2 November 2019

H L Paulson

5

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2 November 2019

N M Bonini

6

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2 November 2019

language of work or name

English

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publication date

1 December 1999

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2 November 2019

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2 November 2019

volume

23

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2 November 2019

issue

4

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2 November 2019

page(s)

425-428

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Protein fate in neurodegenerative proteinopathies: polyglutamine diseases join the (mis)fold

2 November 2019

cites work

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Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

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Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone

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Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease

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Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila

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Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients

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Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

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Molecular chaperones in cellular protein folding

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Conserved features of eukaryotic hsp70 genes revealed by comparison with the nucleotide sequence of human hsp70

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Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice

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Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

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Tissue-specific expression of dominant negative mutant Drosophila HSC70 causes developmental defects and lethality

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Chaperone-supervised conversion of prion protein to its protease-resistant form

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Hsp104, Hsp70, and Hsp40: a novel chaperone system that rescues previously aggregated proteins

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Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons.

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Genetic Transformation of Drosophila with Transposable Element Vectors

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