Proteasome mapping reveals sexual dimorphism in tissue-specific sensitivity to protein aggregations

EMBO Rep. 2020 Apr 3;21(4):e48978. doi: 10.15252/embr.201948978. Epub 2020 Feb 23.

Abstract

Defects in the proteasome can result in pathological proteinopathies. However, the pathogenic role of sex- and tissue-specific sensitivity to proteotoxic stress remains elusive. Here, we map the proteasome activity across nine tissues, in male and female mice, and demonstrate strong sexual dimorphism in proteasome activity, where females have significantly higher activity in several tissues. Further, we report drastic differences in proteasome activity among tissues, independently of proteasome concentration, which are exacerbated under stress conditions. Sexual dimorphism in proteasome activity is confirmed in a SOD1 ALS mouse model, in which the spinal cord, a tissue with comparatively low proteasome activity, is severely affected. Our results offer mechanistic insight into tissue-specific sensitivities to proteostasis stress and into sex differences in the progression of neurodegenerative proteinopathies.

Keywords: amyotrophic lateral sclerosis; gender differences; proteasome; protein aggregates; ubiquitin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amyotrophic Lateral Sclerosis*
  • Animals
  • Disease Models, Animal
  • Female
  • Male
  • Mice
  • Mice, Transgenic
  • Proteasome Endopeptidase Complex / genetics
  • Protein Aggregates
  • Sex Characteristics*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase-1 / genetics

Substances

  • Protein Aggregates
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • Proteasome Endopeptidase Complex