U1-independent pre-mRNA splicing contributes to the regulation of alternative splicing

Nucleic Acids Res. 2009 Apr;37(6):1907-14. doi: 10.1093/nar/gkp050. Epub 2009 Feb 3.

Abstract

U1 snRNP plays a crucial role in the 5' splice site recognition during splicing. Here we report the first example of naturally occurring U1-independent U2-type splicing in humans. The U1 components were not included in the pre-spliceosomal E complex formed on the human F1gamma (hF1gamma) intron 9 in vitro. Moreover, hF1gamma intron 9 was efficiently spliced even in U1-disrupted Xenopus oocytes as well as in U1-inactivated HeLa nuclear extracts. Finally, hF1gamma exon 9 skipping induced by an alternative splicing regulator Fox-1 was impaired when intron 9 was changed to the U1-dependent one. Our results suggest that U1-independent splicing contributes to the regulation of alternative splicing of a class of pre-mRNAs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Animals
  • Exons
  • HeLa Cells
  • Humans
  • Proton-Translocating ATPases / genetics
  • RNA Precursors / metabolism*
  • RNA Splice Sites
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / metabolism
  • Ribonucleoprotein, U1 Small Nuclear / metabolism*
  • Spliceosomes / metabolism*
  • Xenopus

Substances

  • RNA Precursors
  • RNA Splice Sites
  • RNA, Messenger
  • RNA-Binding Proteins
  • Ribonucleoprotein, U1 Small Nuclear
  • gamma subunit, F(1) ATPase
  • Proton-Translocating ATPases