mRNA turnover makes significant contributions to the control of gene e
xpression. Recent studies of mRNA turnover in the simple eukaryote Sac
charomyces cerevisiae have led to a better understanding of this proce
ss. These studies suggest that half-lives of individual transcripts ar
e determined in large part by the interplay between specific sequences
within mRNAs and less defined features of an mRNA, such as translatio
n rate. These studies also indicate that yeast mRNAs are degraded thro
ugh a diverse set of decay pathways. The most common of these pathways
is deadenylation-dependent decapping, in which transcripts are deaden
ylated, thereby promoting decapping and exposing the transcript to 5'-
to-3' exonucleolytic digestion. Additional pathways of mRNA decay incl
ude deadenylation-independent decapping 3'-to-5' degradation and possi
bly endonucleolytic cleavage. Recent experiments have also begun to id
entify some of the trans-acting factors responsible for both performin
g and regulating the nucleolytic events in these various pathways. Fur
ther identification of additional trans-acting factors that function i
n mRNA decay and the development of yeast cell-free systems capable of
reproducing in vivo mRNA turnover are major challenges to be addresse
d.