Towards understanding RNA-mediated neurological disorders

J Genet Genomics. 2014 Sep 20;41(9):473-84. doi: 10.1016/j.jgg.2014.08.003. Epub 2014 Aug 23.

Abstract

RNA-mediated mechanisms of disease pathogenesis in neurological disorders have been recognized in the context of certain repeat expansion disorders. This RNA-initiated neurodegeneration may play a more pervasive role in disease pathology beyond the classic dynamic mutation disorders. Here, we review the mechanisms of RNA toxicity and aberrant RNA processing that have been implicated in ageing-related neurological disorders. We focus on diseases with aberrant sequestration of RNA-binding proteins, bi-directional transcription, aberrant translation of repeat expansion RNA transcripts (repeat-associated non-ATG (RAN) translation), and the formation of pathological RNA:DNA secondary structure (R-loop). It is likely that repeat expansion disorders arise from common mechanisms caused by the repeat expansion mutations. However, the context of the repeat expansion determines the specific molecular consequences, leading to clinically distinct disorders.

Keywords: Neurodegeneration; R-loop; RAN translation; RNA toxicity; Repeat expansion.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Humans
  • Nervous System Diseases / genetics*
  • Nervous System Diseases / metabolism
  • Nervous System Diseases / therapy
  • Protein Biosynthesis
  • RNA / genetics*
  • RNA / metabolism
  • RNA-Binding Proteins / metabolism
  • Transcription, Genetic

Substances

  • RNA-Binding Proteins
  • RNA