Quantitative microarray profiling provides evidence against widespread coupling of alternative splicing with nonsense-mediated mRNA decay to control gene expression

Genes Dev. 2006 Jan 15;20(2):153-8. doi: 10.1101/gad.1382806.

Abstract

Sequence-based analyses have predicted that approximately 35% of mammalian alternative splicing (AS) events produce premature termination codon (PTC)-containing splice variants that are targeted by the process of nonsense-mediated mRNA decay (NMD). This led to speculation that AS may often regulate gene expression by activating NMD. Using AS microarrays, we show that PTC-containing splice variants are generally produced at uniformly low levels across diverse mammalian cells and tissues, independently of the action of NMD. Our results suggest that most PTC-introducing AS events are not under positive selection pressure and therefore may not contribute important functional roles.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Animals
  • Codon, Nonsense / genetics
  • Codon, Nonsense / metabolism*
  • Computational Biology
  • Gene Expression Regulation*
  • HeLa Cells
  • Humans
  • Mice
  • Oligonucleotide Array Sequence Analysis*
  • Open Reading Frames
  • RNA Helicases / metabolism
  • RNA Stability
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Trans-Activators
  • Transfection

Substances

  • Codon, Nonsense
  • RNA, Messenger
  • Rent1 protein, mouse
  • Trans-Activators
  • RNA Helicases
  • UPF1 protein, human