Purification by affinity chromatography of H1o RNA-binding proteins from rat brain

Int J Mol Med. 2003 Apr;11(4):509-13.

Abstract

Post-transcriptional regulation of mRNA metabolism is involved in processes as different as cell fate specification in development and cell response to a large variety of environmental cues. Regulation of all steps of RNA metabolism depends on RNA-binding proteins (RBPs). By using a T1 RNase-protection assay, we previously identified three H1 degrees RNA-binding factors (p40, p70 and p110), highly expressed in the rat brain. Here we report enrichment of these factors from brain extracts, obtained by affinity chromato-graphy of biotinylated H1 degrees RNA-protein complexes on streptavidin-conjugated paramagnetic particles. The purified proteins maintain RNA-binding ability and preference for histone messages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Chromatography, Affinity
  • HSP40 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins / metabolism
  • Heat-Shock Proteins / metabolism
  • Molecular Sequence Data
  • RNA / metabolism
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / isolation & purification*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • HSP40 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins
  • Heat-Shock Proteins
  • RNA-Binding Proteins
  • RNA

Associated data

  • GENBANK/X70685
  • GENBANK/X73683