Abstract

Nonsense-mediated mRNA decay is a eukaryotic pathway that degrades transcripts with premature termination codons (PTCs). In most eukaryotes, thousands of transcripts are degraded by NMD, including many important regulators of developmental and stress response pathways. Transcripts can be targeted to NMD by the presence of an upstream ORF or by introduction of a PTC through alternative splicing. Many factors involved in the recognition of PTCs and the destruction of NMD targets have been characterized. While some are highly conserved, others have been repeatedly lost in eukaryotic lineages. Here, I detail the factors involved in NMD, our current understanding of their interactions and how they have evolved. I outline a classification system to describe NMD pathways based on the presence/absence of key NMD factors. These types of NMD pathways exist in multiple different lineages, indicating the plasticity of the NMD pathway through recurrent losses of NMD factors during eukaryotic evolution. By classifying the NMD pathways in this way, gaps in our understanding are revealed, even within well studied organisms. Finally, I discuss the likely driving force behind the origins of the NMD pathway before the appearance of the last eukaryotic common ancestor: transposable element expansion and the consequential origin of introns.

Highlights

  • Nonsense-mediated mRNA decay is a eukaryotic pathway that degrades transcripts with premature termination codons (PTCs)

  • In particular new information relating to the proteinprotein interactions of UPF1 and SMG5/6/7 family members was added in yeast and animals because evidence for direction, phosphorylation-independent interactions informs us of how to view the mechanism and evolution of nonsense-mediated mRNA decay (NMD), especially regarding the role of SMG1 and how it could have been independently lost multiple times throughout eukaryotic evolution

  • I propose that the classical NMD involves UPF1-3, the UPF1-kinase SMG1 and the SMG5/6/7 family

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Summary

15 Aug 2018 report report report report

Any reports and responses or comments on the article can be found at the end of the article. Mammalian SMG6 has been found to bind UPF1 independent of phosphorylation, suggesting some level of conservation of phosphorylation-independent recruitment of decay factors in NMD It is not clear why a phosphorylation checkpoint is needed for NMD in some organisms like mammals and plants, but likely not others such as yeast, but direct interaction seems likely to be the mechanism. The EJC mode has even found support in plants, with reporter genes and transcriptomewide studies supporting a role for exon-exon junctions in 3’ UTRs eliciting NMD47,85–87 These findings would suggest that the EJC mode is an ancient mechanism for targeting transcripts to NMD. Future research efforts can resolve these and other unknowns surrounding NMD

Conclusion
16. Ponting CP
Figure 3
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