A conserved role for cytoplasmic poly(A)-binding protein 1 (PABPC1) in nonsense-mediated mRNA decay

EMBO J. 2007 Mar 21;26(6):1591-601. doi: 10.1038/sj.emboj.7601588. Epub 2007 Feb 22.


The nonsense-mediated mRNA decay (NMD) pathway degrades mRNAs with premature translation termination codons (PTCs). The mechanisms by which PTCs and natural stop codons are discriminated remain unclear. We show that the position of stops relative to the poly(A) tail (and thus of PABPC1) is a critical determinant for PTC definition in Drosophila melanogaster. Indeed, tethering of PABPC1 downstream of a PTC abolishes NMD. Conversely, natural stops trigger NMD when the length of the 3' UTR is increased. However, many endogenous transcripts with exceptionally long 3' UTRs escape NMD, suggesting that the increase in 3' UTR length has co-evolved with the acquisition of features that suppress NMD. We provide evidence for the existence of 3' UTRs conferring immunity to NMD. We also show that PABPC1 binding is sufficient for PTC recognition, regardless of cleavage or polyadenylation. The role of PABPC1 in NMD must go beyond that of providing positional information for PTC definition, because its depletion suppresses NMD under conditions in which translation efficiency is not affected. These findings reveal a conserved role for PABPC1 in mRNA surveillance.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • 3' Untranslated Regions / metabolism*
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Cell Line
  • Codon, Nonsense / genetics
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / metabolism
  • Poly(A)-Binding Protein I / metabolism*
  • RNA Interference
  • RNA Stability / genetics
  • RNA Stability / physiology*
  • RNA, Messenger / metabolism*


  • 3' Untranslated Regions
  • Codon, Nonsense
  • Poly(A)-Binding Protein I
  • RNA, Messenger