Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones

Maria Udan-Johns, Rocio Bengoechea, Shaughn Bell, Jieya Shao, Marc I. Diamond, Heather L. True, Conrad C. Weihl, Robert H. Baloh

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

TDP-43 aggregation in the cytoplasm or nucleusis a key feature of the pathology of amyotrophic lateral sclerosis and frontotemporal dementia and is observed in numerous other neurodegenerative diseases, including Alzheimer's disease. Despite this fact, the inciting events leading to TDP-43 aggregation remain unclear. We observed that endogenous TDP-43 undergoes reversible aggregation in the nucleus after the heat shock and that this behavior is mediated by the C-terminal prion domain. Substitution of the prion domain from TIA-1 or an authentic yeast prion domain from RNQ1 into TDP-43 can completely recapitulate heat shock-induced aggregation. TDP-43 is constitutively bound to members of the Hsp40/Hsp70 family, and we found that heat shockinduced TDP-43 aggregation is mediated by the availability of these chaperones interacting with the inherently disordered C-terminal prion domain. Finally, we observed that the aggregation of TDP-43 during heat shock led to decreased binding tohnRNPA1, and a change in TDP-43 RNA-binding partners suggesting that TDP-43 aggregation alters its function in response to misfolded protein stress. These findings indicate that TDP-43 shares properties with physiologic prions from yeast, in that self-aggregation is mediated by a Q/N-rich disordered domain, is modulated by chaperone proteins and leads to altered function of the protein. Furthermore, they indicate that TDP-43 aggregation is regulated by chaperone availability, explaining the recurrent observation of TDP-43 aggregates in degenerative diseases of both the brain and muscle where protein homeostasis is disrupted.

Original languageEnglish (US)
Article numberddt408
Pages (from-to)157-170
Number of pages14
JournalHuman Molecular Genetics
Volume23
Issue number1
DOIs
StatePublished - Jan 2014

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Prions
Shock
Hot Temperature
Yeasts
Muscle Proteins
Brain Diseases
Heat-Shock Proteins
Neurodegenerative Diseases
Alzheimer Disease
Cytoplasm
Proteins
Homeostasis
Observation
RNA
Pathology

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)
  • Molecular Biology

Cite this

Udan-Johns, M., Bengoechea, R., Bell, S., Shao, J., Diamond, M. I., True, H. L., ... Baloh, R. H. (2014). Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones. Human Molecular Genetics, 23(1), 157-170. [ddt408]. https://doi.org/10.1093/hmg/ddt408

Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones. / Udan-Johns, Maria; Bengoechea, Rocio; Bell, Shaughn; Shao, Jieya; Diamond, Marc I.; True, Heather L.; Weihl, Conrad C.; Baloh, Robert H.

In: Human Molecular Genetics, Vol. 23, No. 1, ddt408, 01.2014, p. 157-170.

Research output: Contribution to journalArticle

Udan-Johns, M, Bengoechea, R, Bell, S, Shao, J, Diamond, MI, True, HL, Weihl, CC & Baloh, RH 2014, 'Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones', Human Molecular Genetics, vol. 23, no. 1, ddt408, pp. 157-170. https://doi.org/10.1093/hmg/ddt408
Udan-Johns, Maria ; Bengoechea, Rocio ; Bell, Shaughn ; Shao, Jieya ; Diamond, Marc I. ; True, Heather L. ; Weihl, Conrad C. ; Baloh, Robert H. / Prion-like nuclear aggregation of TDP-43 during heat shock is regulated by HSP40/70 chaperones. In: Human Molecular Genetics. 2014 ; Vol. 23, No. 1. pp. 157-170.
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