Toxic effects of mutant huntingtin in axons are mediated by its proline-rich domain

Brain. 2024 Jun 3;147(6):2098-2113. doi: 10.1093/brain/awad280.

Abstract

Huntington's disease results from expansion of a polyglutamine tract (polyQ) in mutant huntingtin (mHTT) protein, but mechanisms underlying polyQ expansion-mediated toxic gain-of-mHTT function remain elusive. Here, deletion and antibody-based experiments revealed that a proline-rich domain (PRD) adjacent to the polyQ tract is necessary for mHTT to inhibit fast axonal transport and promote axonal pathology in cultured mammalian neurons. Further, polypeptides corresponding to subregions of the PRD sufficed to elicit the toxic effect on fast axonal transport, which was mediated by c-Jun N-terminal kinases (JNKs) and involved PRD binding to one or more SH3-domain containing proteins. Collectively, these data suggested a mechanism whereby polyQ tract expansion in mHTT promotes aberrant PRD exposure and interactions of this domain with SH3 domain-containing proteins including some involved in activation of JNKs. In support, biochemical and immunohistochemical experiments linked aberrant PRD exposure to increased JNK activation in striatal tissues of the zQ175 mouse model and from post-mortem Huntington's disease patients. Together, these findings support a critical role of PRD on mHTT toxicity, suggesting a novel framework for the potential development of therapies aimed to halt or reduce axonal pathology in Huntington's disease.

Keywords: Huntington’s disease; JNK3; SH3-binding domain; axonal transport; huntingtin; proline-rich domain.

MeSH terms

  • Animals
  • Axonal Transport
  • Axons* / metabolism
  • Axons* / pathology
  • Cells, Cultured
  • Disease Models, Animal
  • Female
  • Humans
  • Huntingtin Protein* / genetics
  • Huntingtin Protein* / metabolism
  • Huntington Disease* / genetics
  • Huntington Disease* / metabolism
  • Huntington Disease* / pathology
  • Male
  • Mice
  • Mice, Transgenic
  • Mutation / genetics
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurons / metabolism
  • Neurons / pathology
  • Peptides / metabolism
  • Proline / genetics
  • Proline / metabolism
  • Proline-Rich Protein Domains

Substances

  • Huntingtin Protein
  • Nerve Tissue Proteins
  • HTT protein, human
  • Peptides
  • Proline