Arginine-rich dipeptide-repeat proteins as phase disruptors in C9-ALS/FTD

Emerg Top Life Sci. 2020 Dec 11;4(3):293-305. doi: 10.1042/ETLS20190167.

Abstract

A hexanucleotide repeat expansion GGGGCC (G4C2) within chromosome 9 open reading frame 72 (C9orf72) is the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia (C9-ALS/FTD). This seminal realization has rapidly focused our attention to the non-canonical translation (RAN translation) of the repeat expansion, which yields dipeptide-repeat protein products (DPRs). The mechanisms by which DPRs might contribute to C9-ALS/FTD are widely studied. Arginine-rich DPRs (R-DPRs) are the most toxic of the five different DPRs produced in neurons, but how do R-DPRs promote C9-ALS/FTD pathogenesis? Proteomic analyses have uncovered potential pathways to explore. For example, the vast majority of the R-DPR interactome is comprised of disease-linked RNA-binding proteins (RBPs) with low-complexity domains (LCDs), strongly suggesting a link between R-DPRs and aberrations in liquid-liquid phase separation (LLPS). In this review, we showcase several potential mechanisms by which R-DPRs disrupt various phase-separated compartments to elicit deleterious neurodegeneration. We also discuss potential therapeutic strategies to counter R-DPR toxicity in C9-ALS/FTD.

Keywords: ALS; FTD; RAN translation; dipeptide-repeat proteins; neurodegeneration; phase separation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Amyotrophic Lateral Sclerosis*
  • Arginine
  • C9orf72 Protein / genetics
  • DNA Repeat Expansion*
  • Dipeptides / genetics
  • Frontotemporal Dementia* / genetics
  • Humans
  • Proteomics

Substances

  • C9orf72 Protein
  • Dipeptides
  • Arginine

Supplementary concepts

  • Amyotrophic Lateral Sclerosis 2, Juvenile