TDP-35 sequesters TDP-43 into cytoplasmic inclusions through binding with RNA

FEBS Lett. 2015 Jul 8;589(15):1920-8. doi: 10.1016/j.febslet.2015.06.009. Epub 2015 Jun 19.

Abstract

TDP-43 (TAR DNA binding protein of 43 kDa) and its C-terminal fragments are thought to be linked to the pathologies of amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Here, we demonstrate that the aggregates or inclusions formed by its 35-kDa fragment (namely TDP-35) sequester full-length TDP-43 into cytoplasmic inclusions; and this sequestration is mediated by binding with RNA that is enriched in the cytoplasmic inclusions. RNA recognition motif 1 (RRM1) of TDP-43/TDP-35 plays a dominant role in nucleic-acid binding; mutation in this moiety abrogates formation of the TDP-35 inclusions and its RNA-assisted association with TDP-43. Thus, TDP-35 is able to sequester TDP-43 from nuclear localization into cytoplasmic inclusions, and RNA binding plays an essential role in this process.

Keywords: C-terminal fragment of ∼35kDa; Cytoplasmic inclusion; RNA recognition motif; Sequestration; TAR DNA binding protein of 43kDa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cytoplasm / metabolism*
  • DNA Primers
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • HEK293 Cells
  • Humans
  • Mutation
  • Peptide Fragments / genetics
  • Peptide Fragments / physiology*
  • Polymerase Chain Reaction
  • Protein Binding
  • RNA / genetics
  • RNA / metabolism*

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • Peptide Fragments
  • TARDBP protein, human
  • RNA