A simple whole cell lysate system for in vitro splicing reveals a stepwise assembly of the exon-exon junction complex

J Biol Chem. 2004 Feb 20;279(8):7009-13. doi: 10.1074/jbc.M307692200. Epub 2003 Nov 18.

Abstract

Pre-mRNA splicing removes introns and leaves in its wake a multiprotein complex near the exon-exon junctions of mRNAs. This complex, termed the exon-exon junction complex (EJC), contains at least seven proteins and provides a link between pre-mRNA splicing and downstream events, including transport, localization, and nonsense-mediated mRNA decay. Using a simple whole cell lysate system we developed for in vitro splicing, we prepared lysates from cells transfected with tagged EJC proteins and studied the association of these proteins with pre-mRNA, splicing intermediates, and mRNA, as well as formation of the EJC during splicing. Three of the EJC components, Aly/REF, RNPS1, and SRm160, are found on pre-mRNA by the time the spliceosome is formed, whereas Upf3b associates with splicing intermediates during or immediately after the first catalytic step of the splicing reaction (cleavage of exon 1 and intron-lariat formation). In contrast, Y14 and magoh, which remain stably associated with mRNA after export to the cytoplasm, join the EJC during or after completion of exon-exon ligation. These findings indicate that EJC formation is an ordered pathway that involves stepwise association of components and is coupled to specific intermediates of the splicing reaction.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Blotting, Western
  • Catalysis
  • Cell Line
  • Cytoplasm / metabolism
  • Exons*
  • Humans
  • In Vitro Techniques
  • Introns
  • Models, Biological
  • Plasmids / metabolism
  • Precipitin Tests
  • RNA Splicing*
  • RNA, Messenger / metabolism
  • Spliceosomes / metabolism
  • Time Factors
  • Transfection

Substances

  • RNA, Messenger