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Vol. 10, Issue 6, 1873-1889, June 1999

and
*Department of Biochemistry, University of Texas Southwestern
Medical Center at Dallas, Dallas, Texas 75235-9038; and
Activated GTP-bound Rab proteins are thought to interact with
effectors to elicit vesicle targeting and fusion events.
Vesicle-associated v-SNARE and target membrane t-SNARE proteins are
also involved in vesicular transport. Little is known about the
functional relationship between Rabs and SNARE protein complexes. We
have constructed an activated allele of VPS21, a yeast
Rab protein involved in vacuolar protein sorting, and demonstrated an
allele-specific interaction between Vps21p and Vac1p. Vac1p was found
to bind the Sec1p homologue Vps45p. Although no association between
Vps21p and Vps45p was seen, a genetic interaction between
VPS21 and VPS45 was observed. Vac1p
contains a zinc-binding FYVE finger that may bind
phosphatidylinositol 3-phosphate [PtdIns(3)P]. In other FYVE domain proteins, this motif and PtdIns(3)P are necessary for membrane association. Vac1 proteins with mutant FYVE fingers still associated with membranes but showed vacuolar protein sorting defects and reduced
interactions with Vps45p and activated Vps21p. Vac1p membrane association was not dependent on PtdIns(3)P, Pep12p, Vps21p, Vps45p, or
the PtdIns 3-kinase, Vps34p. Vac1p FYVE finger mutant missorting phenotypes were suppressed by a defective allele of
VPS34. These data indicate that PtdIns(3)P may perform a
regulatory role, possibly involved in mediating Vac1p protein-protein
interactions. We propose that activated-Vps21p interacts with its
effector, Vac1p, which interacts with Vps45p to regulate the Golgi to
endosome SNARE complex.
Department of Biology, Utah State University, Logan, Utah
84322-5305
Corresponding author. E-mail
address: bhoraz{at}biochem.swmed.edu.
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