Engineered NLS-chimera downregulates expression of aggregation-prone endogenous FUS

Nat Commun. 2024 Sep 10;15(1):7887. doi: 10.1038/s41467-024-52151-6.

Abstract

Importin β-superfamily nuclear import receptors (NIRs) mitigate mislocalization and aggregation of RNA-binding proteins (RBPs), like FUS and TDP-43, which are implicated in neurodegenerative diseases. NIRs potently disaggregate RBPs by recognizing their nuclear localization signal (NLS). However, disease-causing mutations in NLS compromise NIR binding and activity. Here, we define features that characterize the anti-aggregation activity of NIR and NLS. We find that high binding affinity between NIR and NLS, and optimal NLS location relative to the aggregating domain plays a role in determining NIR disaggregation activity. A designed FUS chimera (FUSIBB), carrying the importin β binding (IBB) domain, is solubilized by importin β in vitro, translocated to the nucleus in cultured cells, and downregulates the expression of endogenous FUS. In this study, we posit that guiding the mutual recognition of NLSs and NIRs will aid the development of therapeutics, illustrated by the highly soluble FUSIBB replacing the aggregation-prone endogenous FUS.

MeSH terms

  • Active Transport, Cell Nucleus
  • Cell Nucleus / metabolism
  • Down-Regulation*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Nuclear Localization Signals*
  • Protein Aggregates
  • Protein Binding
  • RNA-Binding Protein FUS* / genetics
  • RNA-Binding Protein FUS* / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • beta Karyopherins* / genetics
  • beta Karyopherins* / metabolism

Substances

  • RNA-Binding Protein FUS
  • Nuclear Localization Signals
  • beta Karyopherins
  • FUS protein, human
  • Protein Aggregates
  • Recombinant Fusion Proteins