Binding proteins for mRNA localization and local translation, and their dysfunction in genetic neurological disease

Curr Opin Neurobiol. 2004 Oct;14(5):574-81. doi: 10.1016/j.conb.2004.08.010.

Abstract

Neurons utilize mRNA transport and local translation as a means to influence development and plasticity. The molecular mechanisms for this mRNA sorting involve the recognition of cis-acting sequences by distinct mRNA binding proteins that have a dual role, acting in both mRNA transport and translational regulation. Other proteins play a part in the assembly of messenger ribonucleoprotein complexes into transport granules. mRNA binding proteins are crucial targets of phosphorylation signals that regulate local translation. Fragile X syndrome and spinal muscular atrophy have emerged as two genetic neurological diseases that could result, in part, from impaired assembly, localization, and translational regulation of these messenger ribonucleoproteins.

Publication types

  • Review

MeSH terms

  • Active Transport, Cell Nucleus / genetics
  • Animals
  • Central Nervous System / metabolism*
  • Central Nervous System / physiopathology
  • Fragile X Syndrome / genetics
  • Fragile X Syndrome / metabolism
  • Heredodegenerative Disorders, Nervous System / genetics*
  • Heredodegenerative Disorders, Nervous System / metabolism
  • Heredodegenerative Disorders, Nervous System / physiopathology
  • Humans
  • Muscular Atrophy, Spinal / genetics
  • Muscular Atrophy, Spinal / metabolism
  • Protein Biosynthesis / genetics
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*

Substances

  • RNA, Messenger
  • RNA-Binding Proteins