p97/UBXD1 Generate Ubiquitylated Proteins That Are Sequestered into Nuclear Envelope Herniations in Torsin-Deficient Cells

Int J Mol Sci. 2022 Apr 21;23(9):4627. doi: 10.3390/ijms23094627.

Abstract

DYT1 dystonia is a debilitating neurological movement disorder that arises upon Torsin ATPase deficiency. Nuclear envelope (NE) blebs that contain FG-nucleoporins (FG-Nups) and K48-linked ubiquitin are the hallmark phenotype of Torsin manipulation across disease models of DYT1 dystonia. While the aberrant deposition of FG-Nups is caused by defective nuclear pore complex assembly, the source of K48-ubiquitylated proteins inside NE blebs is not known. Here, we demonstrate that the characteristic K48-ubiquitin accumulation inside blebs requires p97 activity. This activity is highly dependent on the p97 adaptor UBXD1. We show that p97 does not significantly depend on the Ufd1/Npl4 heterodimer to generate the K48-ubiquitylated proteins inside blebs, nor does inhibiting translation affect the ubiquitin sequestration in blebs. However, stimulating global ubiquitylation by heat shock greatly increases the amount of K48-ubiquitin sequestered inside blebs. These results suggest that blebs have an extraordinarily high capacity for sequestering ubiquitylated protein generated in a p97-dependent manner. The p97/UBXD1 axis is thus a major factor contributing to cellular DYT1 dystonia pathology and its modulation represents an unexplored potential for therapeutic development.

Keywords: DYT1; ERAD; TorsinA; UBXD1; Ufd1/Npl4; YOD1; dystonia; p97; ubiquitin.

MeSH terms

  • Adaptor Proteins, Vesicular Transport* / genetics
  • Adaptor Proteins, Vesicular Transport* / metabolism
  • Adenosine Triphosphatases* / metabolism
  • Autophagy-Related Proteins* / genetics
  • Autophagy-Related Proteins* / metabolism
  • Cell Membrane Structures / metabolism
  • Dystonia Musculorum Deformans
  • Dystonia* / genetics
  • Dystonia* / metabolism
  • Humans
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Nuclear Envelope* / metabolism
  • Nuclear Pore Complex Proteins / metabolism
  • Nuclear Proteins* / genetics
  • Nuclear Proteins* / metabolism
  • Ubiquitin / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Autophagy-Related Proteins
  • Molecular Chaperones
  • Nuclear Pore Complex Proteins
  • Nuclear Proteins
  • TOR1A protein, human
  • UBXN6 protein, human
  • Ubiquitin
  • Adenosine Triphosphatases
  • p97 ATPase

Supplementary concepts

  • Dystonia musculorum deformans type 1