Recent evidence supports the idea that pre-mRNA splicing and
mRNA export are mechanistically coupled. In metazoans, this
process appears to be mediated by a multicomponent complex,
which associates with the spliced RNA upstream of the
exon–exon junction. One of these components (Aly/REF)
has a homolog in the budding yeast Saccharomyces
cerevisiae known as Yra1p. The YRA1 gene is essential
for growth and required for mRNA export. Notably, YRA1
is one of the only ∼5% intron-containing genes in yeast.
Moreover, the YRA1 intron has several unusual features
and is conserved in other budding yeast species. Previously,
overexpression of intronless YRA1 was shown to be toxic.
We show here that overexpression of the intron-containing gene
results in increased levels of unspliced pre-mRNA but normal
levels of Yra1 protein; conversely, expression of the cDNA results
in increased levels of protein and accumulation of nuclear
poly(A)+ RNA. Two additional lines of evidence suggest
that expression of Yra1p is autoregulated: First, expression
of excess Yra1p from a plasmid reduces the level of tagged,
chromosomal Yra1p, and, second, this effect requires wild-type
protein. Replacement of the YRA1 intron with that of
other S. cerevisiae genes cannot rescue the
dominant-negative growth defect of intronless YRA1.
We conclude that the level of Yra1p is negatively autoregulated
by a mechanism that involves splicing of its unusual intron.
Tight control of the levels of Yra1p might be necessary to couple
the rates of pre-mRNA splicing and mRNA export.