In growing cells of the yeast Saccharomyces cerevisiae, proaminopeptidase I
reaches the vacuole via the selective cytoplasm-to-vacuole targeting (cvt)
pathway. During nutrient limitation, autophagy is also responsible for the
transport of proaminopeptidase I. These two nonclassical protein transport
pathways to the vacuole are distinct in their characteristics but in large
part use identical components. We expanded our initial screen for aut(-) m
utants and isolated aut9-1 cells, which show a defect in both pathways, the
vacuolar targeting of proaminopeptidase I and autophagy. By complementatio
n of the sporulation defect of homocygous diploid aut9-1 mutant cells with
a genomic library, in this study we identified and characterized the AUT9 g
ene, which is allelic with CVT7. aut9-deficient cells have no obvious defec
ts in growth on rich media, vacuolar biogenesis, and acidification, but lik
e other mutant cells with a defect in autophagy, they exhibit a reduced sur
vival rate and reduced total protein turnover during starvation. Aut9p is t
he first putative integral membrane protein essential for autophagy. A biol
ogically active green fluorescent protein-Aut9 fusion protein was visualize
d at punctate structures in the cytosol of growing cells.