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Mol. Cell. Biol., Feb 1995, 809-823, Vol 15, No. 2
KW Hagan, MJ Ruiz-Echevarria, Y Quan and SW Peltz
Several lines of evidence indicate that the processes of mRNA turnover and
translation are intimately linked and that understanding this relationship
is critical to elucidating the mechanism of mRNA decay. One clear example
of this relationship is the observation that nonsense mutations can
accelerate the decay of mRNAs in a process that we term nonsense-mediated
mRNA decay. The experiments described here demonstrate that in the yeast
Saccharomyces cerevisiae premature translational termination within the
initial two-thirds of the PGK1 coding region accelerates decay of that
transcript regardless of which of the stop codons is used. Nonsense
mutations within the last quarter of the coding region have no effect on
PGK1 mRNA decay. The sequences required for nonsense-mediated mRNA decay
include a termination codon and specific sequences 3' to the nonsense
mutation. Translation of two- thirds of the PGK1 coding region inactivates
the nonsense-mediated mRNA decay pathway. This observation explains why
carboxyl-terminal nonsense mutations are resistant to accelerated decay.
Characterization of the decay of nonsense-containing HIS4 transcripts
yielded results mirroring those described above, suggesting that the
sequence requirements described for the PGK1 transcript are likely to be a
general characteristic of this decay pathway. In addition, an analysis of
the decay intermediates of nonsense-containing mRNAs indicates that
nonsense-mediated mRNA decay flows through a pathway similar to that
described for a class of wild-type transcripts. The initial cleavage event
occurs near the 5' terminus of the nonsense-containing transcript and is
followed by 5'-->3' exonucleolytic digestion. A model for
nonsense-mediated mRNA decay based on these results is discussed.
Copyright © 1995, American Society for Microbiology
Characterization of cis-acting sequences and decay intermediates involved in nonsense-mediated mRNA turnover
Department of Molecular Genetics and Microbiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854.
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