Pathogenesis of polyglutamine diseases: Piecing together a complex molecular puzzle

J Exp Med. 2026 Jan 5;223(1):e20241336. doi: 10.1084/jem.20241336. Epub 2025 Oct 23.

Abstract

Polyglutamine (polyQ) diseases, caused by a CAG repeat expansion encoding a glutamine tract in nine distinct proteins, present a complex molecular puzzle in which each piece contributes to neurodegeneration. While each of the causative proteins has a distinct function, the downstream consequences of polyQ toxicity are often similar, including protein accumulation, transcriptional dysregulation, somatic CAG repeat instability, disrupted energy homeostasis, compromised synaptic function, and selective neuronal death. This review summarizes emerging insights into how proteins with an expanded polyQ tract disrupt distinct cellular functions, and we examine a multitude of discoveries that are inspiring and reshaping novel therapeutic strategies.

Publication types

  • Review

MeSH terms

  • Animals
  • Humans
  • Neurodegenerative Diseases* / genetics
  • Neurodegenerative Diseases* / metabolism
  • Neurodegenerative Diseases* / pathology
  • Peptides* / genetics
  • Peptides* / metabolism
  • Trinucleotide Repeat Expansion / genetics

Substances

  • polyglutamine
  • Peptides