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Vol. 15, Issue 7, 3196-3209, July 2004

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Soi3p/Rav1p Functions at the Early Endosome to Regulate Endocytic Trafficking to the Vacuole and Localization of Trans-Golgi Network Transmembrane Proteins

György Sipos ^*  , Jason H. Brickner ^*  , E.J. Brace ^*, Linyi Chen ^|| ¶, Alain Rambourg ^#, Francois Kepes ^# @, and Robert S. Fuller ^* **

^* Department of Biological Chemistry, University of Michigan Medical Center, Ann Arbor, Michigan 48109-0606; ^|| Department of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan 48201, France; and ^# Departement de Biologie Cellulaire et Moleculaire, Commissariat á l'Energie Atomique Saclay, Gif-sur-Yvette 91191 Cedex, France

Submitted October 22, 2003; Revised April 5, 2004; Accepted April 7, 2004
Monitoring Editor: Randy Schekman

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION ACKNOWLEDGMENTS REFERENCES

 
SOI3 was identified by a mutation, soi3-1, that suppressed a mutant trans-Golgi network (TGN) localization signal in the Kex2p cytosolic tail. SOI3, identical to RAV1, encodes a protein important for regulated assembly of vacuolar ATPase. Here, we show that Soi3/Rav1p is required for transport between the early endosome and the late endosome/prevacuolar compartment (PVC). By electron microscopy, soi3-1 mutants massively accumulated structures that resembled early endosomes. soi3 mutants exhibited a kinetic delay in transfer of the endocytic tracer dye FM4-64, from the 14°C endocytic intermediate to the vacuole. The soi3 mutation delayed vacuolar degradation but not internalization of the a-factor receptor Ste3p. By density gradient fractionation, Soi3/Rav1p associated as a peripheral protein with membranes of a density characteristic of early endosomes. The soi3 null mutation markedly reduced the rate of Kex2p transport from the TGN to the PVC but had no effect on vacuolar protein sorting or cycling of Vps10p. These results suggest that assembly of vacuolar ATPase at the early endosome is required for transport of both Ste3p and Kex2p from the early endosome to the PVC and support a model in which cycling through the early endosome is part of the normal itinerary of Kex2p and other TGN-resident proteins.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION ACKNOWLEDGMENTS REFERENCES

 
Steady-state localization of trans-Golgi network (TGN) membrane proteins in the budding yeast Saccharomyces cerevisiae is achieved by continuous cycles of vesicular transport between the TGN and post-TGN compartments such as the late endosome or prevacuolar compartment (PVC) (Fuller et al., 1988; Vida et al., 1993; Cereghino et al., 1995; Brickner and Fuller, 1997; Bryant and Stevens, 1997). Kex2p and Ste13p, proteolytic processing enzymes involved in maturation of -mating factor and other substrates (Fuller et al., 1988), are localized to the TGN by the function of TGN localization signals (TLSs) in their cytosolic tails (C-tails) (Brickner and Fuller, 1997; Bryant and Stevens, 1997). TLS1 directs retrieval from the PVC to the TGN and consists of two essential aromatic residues separated by a nonessential charged or polar residue (Tyr₇₁₃Glu₇₁₄Phe₇₁₅ for Kex2p and Phe₈₅Gln₈₆Phe₈₇ for Ste13p) (Wilcox et al., 1992; Nothwehr et al., 1993; Redding et al., 1996a). Substitutions for Tyr₇₁₃ in the TLS1 of Kex2p leads to loss of TGN localization and rapid delivery of the protein to the vacuole (Wilcox et al., 1992; Redding et al., 1996a). A less well defined signal, TLS2, requires sequences distal to TLS1 in the Kex2p C-tail and functions to delay transport of Kex2p from the TGN to the PVC, possibly by promoting TGN retention (Brickner and Fuller, 1997). A signal similar to TLS2 is found in the Ste13p C-tail (Bryant and Stevens, 1997).

Using a mating assay sensitive to the efficiency of -factor processing by Kex2p, we isolated allele-specific mutant suppressors soi1, SOI2, and soi3 that suppressed the effects of a TLS1 point mutation (Y₇₁₃A) in Kex2p but not of a deletion of TLS1 or of the entire C-tail (Redding et al., 1996a). These soi mutations also suppressed effects of point mutations in the Ste13p TLS1 signal (Redding et al., 1996a). Cloning of SOI1, allelic to VPS13, revealed that this gene encoded a novel 350-kDa peripheral membrane protein whose human homologues include two disease loci (Brickner and Fuller, 1997; Rampoldi et al., 2001; Ueno et al., 2001; Kolehmainen et al., 2003). Suppression of the mislocalization of Y₇₁₃A Kex2p by a soi1 mutation required TLS2, indicating that TLS2 function became activated in the absence of Soi1p, slowing the escape of Kex2p from the TGN (Brickner and Fuller, 1997). The soi1 mutants also displayed defective TLS1-dependent localization, resulting in aberrant localization not only of Kex2p but also of the vacuolar precursor sorting receptor Vps10p and of A-ALP, a hybrid protein in which the Ste13p C-tail is fused to alkaline phosphatase (ALP). These results indicated that Soi1p acts both at the PVC to stimulate TLS1 function and at the TGN to repress TLS2 function and consequently facilitates cycling of transmembrane proteins between the TGN and PVC (Brickner and Fuller, 1997).

Transport of Kex2p from the TGN to the PVC requires clathrin and the dynamin homolog Vps1p (Seeger and Payne, 1992; Wilsbach and Payne, 1993; Nothwehr et al., 1995; Redding et al., 1996a,b). Mutations in two types of clathrin adaptors affect Kex2p localization. These are the Gga proteins, encoded by GGA1 and GGA2, and the Adaptor Protein (AP)-1 adaptor complex (Black and Pelham, 2001). Mutations in the GGA genes blocked transport of carboxypeptidase Y (CPY) to the vacuole, abrogated TGN to PVC transport of Vps10p and Pep12p, and altered the efficiency of pro--factor processing by Kex2p (Black and Pelham, 2000; Dell'Angelica et al., 2000; Hirst et al., 2000; Costaguta et al., 2001). Effects of mutations in genes encoding AP-1 subunits are only seen in combination with either gga mutations or clathrin mutations (Phan et al., 1994; Stepp et al., 1995; Huang et al., 1999; Yeung et al., 1999), suggesting that the transport pathway governed by AP-1 is either less important for Kex2p localization or is redundant with other pathways. Recently, it has been suggested that AP-1 adaptors function in transport between the TGN and early endosome of Kex2p, Ste13p, and chitin synthase III (Chs3p), suggesting that TGN membrane proteins such as Kex2p and Ste13p access the early endosome (Valdivia et al., 2002; Ha et al., 2003).

Here, we have cloned the SOI3 gene, which we find to be identical to RAV1. Rav1p was isolated as a Skp1p-interacting protein that is part of a complex that contains Rav2p and the V₁ subcomplex of the proton-translocating vacuolar ATPase (V-ATPase) (Seol et al., 2001; Smardon et al., 2002). Both RAV1 and RAV2 were shown to be important for glucose-regulated assembly of V₁ onto V₀ to form functional V-ATPase on the vacuolar membrane (Seol et al., 2001). Analysis of the effects of soi3 mutations demonstrates that loss of Soi3p function results both in alterations in the localization of TGN membrane proteins as well as selective defects in delivery of endocytic cargo to the vacuole. A synthesis of these results suggests that assembly of vacuolar ATPase at the early endosome in yeast is essential for early endosome maturation and efficient transport from the early endosome to the PVC.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION ACKNOWLEDGMENTS REFERENCES

 
Antibodies and Reagents
Antisera against the Kex2 Ctail and lumenal domains were as described previously (Wilcox and Fuller, 1991; Wilcox et al., 1992). Anti-Pep12 and anti-CPY monoclonal antibodies were from Molecular Probes (Eugene, OR). Anti-hemagglutinin (HA) monoclonal antibody 12CA5 was from Roche Diagnostics (Indianapolis, IN). Antisera against Anp1p, Mnn1p, Chs3p, Pep12p, Vps10p, CPY, ALP, aminopeptidase I (API), and Ste3p were gifts of Drs. S. Munro (Medical Research Council, Cambridge, United Kingdom), T. Graham (Vanderbilt University, Nashville, TN), R. Schekman (University of California, Berkeley, CA), S. Emr (University of California, San Diego, CA), D. Klionsky (University of Michigan, Ann Arbor, MI), and N. Davis (Wayne State University, Detroit, MI). Antibodies against Ste3p were affinity purified as described previously (Redding et al., 1991; Roth et al., 1998). Rabbit anti-mouse IgG was from Jackson ImmunoResearch Laboratories (West Grove, PA), and horseradish peroxidase-conjugated secondary antibodies were from Amersham Biosciences (Piscataway, NJ). Boc-Leu-Lys-Arg-7-amino-4-methylcoumarin (LKR-AMC) was from Bachem Biosciences (King of Prussia, PA). Restriction and DNA modification enzymes were from New England Biolabs (Beverly, MA). Unless indicated otherwise, all other chemicals and reagents were from Sigma-Aldrich (St. Louis, MO).

Strains and Plasmids
Plasmids containing KEX2 under the KEX2 promoter on yeast centromere plasmids were pCWKX10 (wild-type Kex2p), pCWKX11 (Y₇₁₃A-Kex2p), and pCWKX10-I718tail (I718tail-Kex2p) (Wilcox et al., 1992; Redding et al., 1996a; Brickner and Fuller, 1997). Plasmids containing KEX2 under the GAL1 promoter on yeast centromere plasmids were pCWKX20 (wild type), pCWKX21 (Y₇₁₃A-Kex2p), pCWKX27 (C-tail-Kex2p), pCWKX20-I718tail (I718tail-Kex2p), and pCWKX21-I718tail (Y₇₁₃A, I718tail-Kex2p) (Wilcox et al., 1992; Redding et al., 1996a; Brickner and Fuller, 1997). Plasmids pRS303-SOI3.1 and pRS313-SOI3 were constructed by ligating an EcoRI fragment containing base pairs 491021-498250 from yeast chromosome X into pRS303 (HIS3 integrating plasmid) and pRS313 (HIS3 CEN ARS plasmid), respectively (Sikorski and Hieter, 1989). Plasmid pSOI3-HA was generated from pRS313-SOI3.1 by mutating the final three codons of SOI3 from GAC TTT GTA to GGC GGC CGC by polymerase chain reaction (PCR) to generate a NotI site and ligating a fragment encoding a triple HA epitope tag (Tyers et al., 1992). Plasmid p413ADH-SOI3 was constructed by PCR amplifying the SOI3 structural gene and ligating the resulting fragment into the EcoRI site of p413ADH (Mumberg et al., 1995). To express a Soi3p fusion to green fluorescent protein (GFP), pSOI3-GFP was created by ligating the 0.75-kb NotI fragment of pSF-GP1 (gift of Jeanne Hirsch, Mt. Sinai School of Medicine, New York, NY) into the NotI site of pRS313-SOI3.1. Plasmids pSOI3-GFP-SL and pSOI3-HA-SL were created by replacing the SacI sites in pSOI3-GFP and pSOI3-HA with a SalI site by linker ligation. Plasmids p413ADH-SOI3-GFP and p413ADH-SOI3-HA were created by ligating the NarI/SalI fragments of pSOI3-GFP-SL and pSOI3-HA-SL containing the C termini of SOI3-GFP and SOI3-HA, into p413ADH-SOI3 cleaved by NarI plus SalI. Expression of Soi3-Soi3-GFP fully complemented the soi3 null mutation (our unpublished data).

Strains used in this study, created by standard genetic crosses and/or by transformation, are shown in Table 1. Yeast media were as described (Rose et al., 1990). Two-step gene replacements were used to convert STE3 either to Gal1-STE3, Gal1-STE3-HA or to Gal1-STE3365, as described previously (Roth and Davis, 1996; Chen and Davis, 2002). To delete VPS1, the complete coding sequence of VPS1 was replaced with Kluyveromyces lactis LEU2 as described previously (Gueldener et al., 2002). The vps1-100-ts allele was introduced by transplacement. Plasmid pCAV40 (generous gift of Tom Stevens, University of Oregon, Portland, OR) containing vps1-100-ts was digested with EcoRI, transformed into CRY1, and Ura⁺ transformants were selected. Ura^- recombinants isolated by 5-fluoroorotic acid selection were tested by the CPY colony blot assay to identify a strain carrying the vps1-100-ts allele (EBY73).

Cloning and Analysis of SOI3
Strain SPB400-3D carrying plasmid pCWKX10 was transformed with the CEN ARS LEU2 genomic library YPH1 (ATCC no. 77162). Library transformants were screened by replica-plating to both YPD + 6 mM ZnCl₂ and YPD + 10 mM ZnCl₂. Zinc-resistant transformants were tested for plasmid dependence and for their ability to complement the Soi⁺ phenotype measured by the onset of impotence experiment as described previously (Redding et al., 1996a). Two independent transformants displayed plasmid-dependent complementation of both the Zn²⁺ sensitivity and the Soi⁺ phenotype (Redding et al., 1996a). DNA sequencing revealed that the inserts corresponded to base pairs 491021-498727 on chromosome X. To determine whether this DNA region corresponded to SOI3, an EcoRI fragment corresponding to base pairs 491021-498250 from chromosome X was cloned into pRS303 (HIS3 integrating plasmid) (Sikorski and Hieter, 1989) to create pRS303-SOI3.1A. This plasmid was linearized with StuI, transformed into KRY18-1B, and His⁺ transformants were crossed to SPB400-3D transformed with pKWKX21. The resulting diploid was sporulated and analyzed by random spore analysis, demonstrating linkage of the integrated marker and soi3-1 (46 MATMAT strains: 0 Soi⁺ His⁺, 12 Soi⁺ His^-, 32 Soi^- His⁺, and 0 Soi^- His^-), also confirmed by tetrad analysis (our unpublished data). DNA sequence analysis of the inserts combined with examination of the published yeast genomic sequence showed that only two full-length open reading frames, YJR033c and PET191, were contained within the overlapping region. YJR033c was seen as the more likely candidate, because soi3-1 strains grew on nonfermentable carbon sources (our unpublished data). However, subclones containing YJR033c along with 232 base pairs of the 5' untranslated region and 220 base pairs of PET191 did not fully complement both the Zn²⁺ sensitivity and suppressor phenotypes (our unpublished data). To confirm that expression of YJR033c alone complemented soi3-1 phenotypes, YJR033c was amplified by PCR and subcloned under the control of the ADH promoter on a single copy CEN plasmid (Mumberg et al., 1995), resulting in plasmid pADH-YJR033c.

Heterozygous replacement of the complete coding sequence of the SOI3 gene with the kan^r gene (Wach et al., 1994) in diploid strain KRY18 resulted in GSY11, which was sporulated to generate haploid soi3 strains (Table 1).

Microscopy
For electron microscopy (EM), cells were fixed, stained, and visualized as described previously (Rambourg et al., 1993). For FM4-64 uptake experiments, strains GSY11-2A (soi3) and GSY11-4D (SOI3) were grown in 10 ml of YPD to OD₆₀₀ = 0.9, harvested, and resuspended in 500 µl of cold YPD + 40 µM FM4-64 (Molecular Probes). Cells were incubated on ice for 1 h, washed in cold YPD, and resuspended in 1 ml of cold YPD and incubated at 14°C, with shaking. After 40 min at 14°C, 500 µl of cells was harvested and resuspended in 400 µl of prewarmed 30°C YPD. Cells were harvested, washed in 1x 100 µl of 10 mM NaN₃, 0 mM NaF, resuspended in 25 µl of 10 mM NaN₃, 10 mM NaF, and stored on ice until they were examined using an Axioskop microscope (Carl Zeiss, Thornwood, NY), recording data on film as described previously (Brickner and Fuller, 1997). Soi3-GFP images were examined using a Nikon Eclipse 800 microscope and an ORCA2 charge-coupled device (Hamamatsu, Bridgewater, NJ). Cells were grown in log phase in minimal medium at 25°C and mounted in low-temperature agarose. Z-stacks were created using eight 0.25-µm steps. ISEE Software (Inovision, Raleigh, NC) was used for image capture and deconvolution of Z-stacks.

Ste3p and Zrt1-HAp Endocytosis
Constitutive turnover of the Ste3p and the a-factor-dependent internalization, recycling, and turnover of Ste3365p were all performed as described previously (Chen and Davis, 2000). Expression of Ste3p and related proteins (Ste3365p and Ste3HAp) was regulated from the GAL1 promoter (Chen and Davis, 2000). Single HA epitope-tagged Zrt1p (Zrt1-HAp) was expressed from its own promoter on plasmid pMC5-HSET (Gitan et al., 1998), a gift of David Eide (University of Missouri, Columbia, MO). To induce Zrt1-HAp in soi3 cells, soi3 and control cells were pretreated with 1 mM EDTA for 3 h to induce Zrt1-HAp expression, and internalization was initiated by the addition of 2 mM Zn²⁺. Cell disruption and sample preparation protocols were as described previously (Davis et al., 1993).

Subcellular Fractionation
Fractionation procedures followed published methods (Sipos and Fuller, 2002). Cells were spheroplasted with lyticase, and 200-µl samples equivalent to 50 ml of cells (OD₆₀₀ = 1) were frozen over liquid N₂. For differential centrifugation, spheroplasts were thawed and homogenized, and lysates were centrifuged twice at 500 x g for 5 min. The supernatant was centrifuged for 15 min at 13,000 x g. The resulting pellet (P13) was washed with buffer and pelleted again for 15 min at 13,000. The medium speed supernatant (S13) was split into three samples. One was adjusted to 1 M NaCl, a second to 1% Triton X-100. These samples were incubated on ice for 20 min and centrifuged in a TLS55 rotor in a TLX centrifuge (Beckman Coulter, Fullerton, CA) at 55,000 rpm (200,000 x g at r_avg) for 30 min to generate P200 and S200 fractions. Samples equivalent to 1 ml of cells (OD₆₀₀ = 1.0) of the P13, S13, P200, and S200 fractions were fractionated by SDS-PAGE, and the presence of markers were analyzed by immunoblotting.

For sucrose gradient fractionation, 0.5 ml of P200 fraction, equivalent to 200 ml of cells (OD₆₀₀ = 1.0), was loaded on the top of the following sucrose step gradient (from the bottom): 0.5 ml of 60%/2.0 ml of 48%/2.5 ml of 40%/2.5 ml of 36%/2.5 ml of 32%/2.0 ml of 29%. The gradient was centrifuged at 41,000 rpm for 17 h at 4°C by using a Beckman Coulter SW41 rotor. Fractions (250 µl) were collected, and 10- to 15-µl samples from each interface were analyzed by immunoblotting and assayed for Kex2 activity, as described previously (Sipos and Fuller, 2002).

³⁵S Pulse-Chase/Immunoprecipitation
³⁵S Pulse-chase/immunoprecipitation experiments were performed essentially as described previously (Wilcox and Fuller, 1991). Cells were labeled with ³⁵S-labeled amino acids (Express Label; Amersham Biosciences). Five-minute pulses were used for ALP, CPY, and API, and 10-min pulses were used for Kex2p and Vps10p. Pulses were followed by chase with nonradioactive methionine and cysteine at 10 mM, and cell samples removed at various times were subjected to glass-bead lysis under denaturing conditions. Immunoprecipitations (IPs) of Kex2p and Vps10p were carried out twice. Other proteins were subjected to single IPs. IPs used polyclonal antisera and Pansorbin (Calbiochem-Novabichem, La Jolla, CA) (2.5 µl of 50% slurry per equivalent of 1 ml of cells at OD₆₀₀ = 1.0). IPs were fractionated by SDS-PAGE, and radioactive signals were captured and quantified using a PhosphorImager (Amersham Biosciences) and IPLabgel software (Signal Analytics, Vienna, VA). Half-lives were calculated by linear regression.

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION ACKNOWLEDGMENTS REFERENCES

 
SOI3 Corresponds to YJR033c/RAV1
Unlike soi1 mutations (Brickner and Fuller, 1997), dominant SOI2 mutations and the recessive soi3-1 mutation (Redding et al., 1996a) suppressed the Y₇₁₃A substitution in TLS1 in the context of a shortened Kex2p C-tail (I718tail) that lacks TLS2 (Figure 1). Neither the SOI2 mutations nor soi3-1 suppressed deletion of the C-tail, suggesting initially that both suppress through TLS1, i.e., by improving retrieval from the PVC back to the TGN. However, further analysis of the soi3 null mutant, detailed in this work, showed that Soi3p functions in a distinct transport step important to Kex2p localization, between the early and late endosome.

View larger version (46K): [in this window] [in a new window]   Figure 1. soi3-1 mutation suppresses a TLS1 mutation in Kex2p in the absence of TLS2. (A) Schematic diagram of Kex2p indicating various C-tail mutants. C-tail ending at 778 is TLS2+; C-tail ending at 772 is TLS2- (Brickner and Fuller, 1997). (B) SOI2 and soi3-1 mutations improve the localization defect of Y713A mutation of Kex2p in the context of both the short (I718tail) and full-length C-tail. KRY18-1A (wild type), JBY135-1C (soi1), KRY200-r2 (SOI2-3), and KRY208-r3 (soi3-1) were transformed either with pCWKX21 (Y713A-Kex2p) or pCWKX21-I718tail (Y713A, I718tail-Kex2p). Cells were shifted from galactose to glucose for 5 h and tested for mating competence (Redding et al., 1996a).

Phenotypic analysis revealed that hypersensitivity to both Zn²⁺ and Co²⁺ cosegregated with the suppressor phenotype caused by the soi3-1 mutation (our unpublished data). Wild-type SOI3 was cloned from a yeast genomic library by complementing the Zn²⁺ hypersensitivity. Two clones (clones 3 and 4) (Figure 2A) contained overlapping inserts, complemented the suppressor phenotype, and were shown by segregation analysis to map to the soi3-1 locus (see MATERIALS AND METHODS). A single yeast open reading frame from this locus, YJR033c, when placed under control of the moderate ADH promoter in the single copy CEN plasmid pADH-YJR033c (see MATERIALS AND METHODS), complemented both the Zn²⁺ hypersensitivity (Figure 2B) and Soi⁺ suppressor phenotypes of soi3-1 (our unpublished data), confirming the identity of YJR033c as SOI3. As described previously (Kraemer et al., 1998; Seol et al., 2001), YJR033c encodes a large protein (150 kDa) homologous to the DmX protein of Drosophila melanogaster and the human homolog DMXL1 2000) (Kraemer et al., 1998; Kraemer et al., 2000). Soi3p, approximately one-half the size of the metazoan homologues, is predicted to contain at least seven WD40 repeat sequences (Smith et al., 1999), whereas DmX and DMLX1 may contain 28-30 WD repeats (Kraemer et al., 2000). The carboxy terminus of the Soi3p sequence suggests the presence of a coiled-coil domain (residues 1311-1340). Soi3p is identical to Rav1p, which was isolated as a Skp1p-interacting protein implicated in assembly of vacuolar ATPase (V-ATPase) (Seol et al., 2001). This work focuses on the role of Soi3/Rav1p in early endosome to PVC transport, but implicit in this is the expectation that it is the role of the protein in V-ATPase assembly at the early endosome that is key. Unpublished data from our laboratory along with published data support the conclusion that V-ATPase mutants have phenotypes similar to those exhibited by soi3 mutants (our unpublished data) (Perzov et al., 2002). Because soi3-1 was described earlier than RAV1 (Redding et al., 1996a; Seol et al., 2001), SOI3 and Soi3p will be used here except where identity between Soi3p with Rav1p needs emphasis.

View larger version (53K): [in this window] [in a new window]   Figure 2. Cloning of SOI3. Zn2+-resistant (Znr) clones were isolated by transforming SPB400-3D (soi3-1) cells carrying pCWKX10 with a yeast CEN ARS genomic library. (A) After the pCWKX10 plasmid was replaced with pCWKX21, Znr clones were tested for the ability to revert the Soi+ phenotype to wild-type. Clones 3 and 4 were able to complement the Soi+ phenotype and both contained the full-length YJR033c ORF. (B) Expression of YJR033c complemented soi3-1 zinc hypersensitivity. Strains SPB400-r8 (soi3-1) containing pCWKX10 and pADH-YJR033c, SPB400-r8 containing pCWKX10 and vector p413ADH and KRY18-1A (SOI3) containing pCWKX10 were streaked on a YPAD plate containing 5 mM ZnCl2.

soi3-1 Accumulates Early Endosome-like Structures
Electron microscopic analysis of the soi3-1 mutant was conducted using thick sections (250 nm) analyzed at tilt angles to permit creation of stereo pairs (Rambourg et al., 1993). The soi3-1 mutant cells massively accumulated ovoid membrane structures that consisted of clusters of basket-like structures formed from anastomosed tubules (Figure 3). Clusters occurred near the vacuole or facing finger-like invaginations of the plasma membrane, suggestive in appearance of early endosomal tubulo-vesicular structures shown to label with positively charged nanogold (Prescianotto-Baschong and Riezman, 1998). These structures, which might be aberrant early or late endosomes, also were found adjacent to the vacuole, and, in some cases, seemed to be fusing with vacuoles (Figure 3, B and C). These structures were distinct from probable lipid particles, which also seemed to accumulate in the soi3-1 mutant (Figure 3D).

View larger version (153K): [in this window] [in a new window]   Figure 3. Aberrant organelles accumulate in soi3-1 cells. Electron microscopy of wild-type (CRY2) (A) and soi3-1 (SPB400-r8) cells (B-D). Black arrowheads indicate the accumulation of fenestrated ovoids (endosome-like structures, B and C) and white arrowheads point to ovoids contiguous with and apparently fusing with vacuoles (B). Asterisks label excess lipid particles also seen in soi3-1 mutants (D).

soi3 Causes a Kinetic Delay in Endocytic Delivery of FM4-64 to the Vacuole
To assess the effects of loss of Soi3p function on bulk-phase endocytosis, soi3 cells were stained, on ice, with the lipophilic fluorescent dye FM4-64, warmed to 14°C, and then treated with sodium azide and sodium fluoride to deplete ATP (Figure 4). At 14°C, FM4-64 was found to accumulate in peripheral, punctate, endocytic structures in both wild-type and soi3 strains, as has been observed previously for cells maintained at 15°C (Vida and Emr, 1995). When cells were then shifted to 30°C for 5 min, FM4-64 chased to the vacuolar membrane in wild-type cells but persisted in punctate structures in soi3 cells. Extensive vacuolar membrane staining was observed in the soi3 cells after 30 min at 30°C, although persistent staining of one or two extravacuolar punctate structures was still apparent (Figure 4). No delay was observed in internalization of FM4-64 from the plasma membrane to internal sites when cells stained on ice were warmed to 30°C (our unpublished data), suggesting that loss of Soi3p results in a decreased rate of trafficking from an early endocytic intermediate to the vacuole.

View larger version (97K): [in this window] [in a new window]   Figure 4. soi3 cells exhibit a kinetic delay in the uptake of FM 4-64 to the vacuole. Cells were preincubated with FM4-64 on ice, washed, and shifted to 14°C for 40 min to allow uptake in the 14°C early endosomal compartment. Cells were shifted to 30°C and at 5 or 30 min, treated with sodium azide plus fluoride, and visualized by fluorescence microscopy. The difference in plasma membrane staining between the wild-type and soi3 strains seen at 5 min in the figure was not a reproducible observation (our unpublished data). Strains were: GSY11-2A (soi3) and GSY11-4D (wild type).

The soi3 Mutant Is Defective in Constitutive Vacuolar Degradation of Ste3p but Not Defective in Internalization or Endocytic Recycling of Ste3p.
The a-factor receptor, Ste3p, undergoes endocytic internalization followed by delivery to the vacuole and degradation. Internalization occurs by two pathways. Constitutive internalization, which occurs in the absence of ligand, depends on ubiquitination within a PEST sequence in the C-terminal cytosoplasmic tail domain of Ste3p and results in a 20-min t_1/2 (Roth and Davis, 1996). Deletion of this PEST region by truncation of 105 residues of the C-terminal domain results in persistence of receptor at the plasma membrane. The truncated receptor, Ste3365p, however, can be induced to undergo internalization by addition of a-factor. Ligand-dependent internalization of Ste3365p leads to its recycling to the cell surface and slow vacuolar degradation. The effect of the soi3 mutation on each of these three pathways of Ste3p metabolism, constitutive endocytosis, ligand-dependent vacuolar turnover, and recycling to the plasma membrane was examined (Figure 5, A-D). Constitutive vacuolar degradation of Ste3p was found to occur with a t_1/2 of 27 min in the WT background. Ste3p was clearly stabilized in the soi3 strain, exhibiting a t_1/2 of 40 min (Figure 5A), indicating that vacuolar delivery by the constitutive internalization pathway was impaired. In contrast, a soi1 strain exhibited kinetics of constitutive vacuolar turnover of Ste3p indistinguishable from wild-type (our unpublished data).

View larger version (30K): [in this window] [in a new window]   Figure 5. Turnover of Ste3p, Ste3365p, and Zrt1HAp in soi3 cells. (A) Constitutive turnover of Ste3p. Ste3p expression was induced with galactose and terminated by the addition of glucose. (B) Ligand-induced turnover of Ste3365p. After induction with galactose followed by a glucose chase (30 min), endocytosis was initiated by addition of a-factor. (C) Internalization assay for Ste3365p. During ligand-dependent endocytosis, the level of internalized Ste3365p was followed by a protease protection assay. (D) Recycling assay for Ste3365p. After internalization was induced by adding a-factor, recycling of Ste3365p to the cell surface was monitored by protease shaving after removal of the a-factor. (A-D) Strains containing GAL1 promoter-driven STE3 and STE3365 genes were GSY32 (GAL1-STE3), GSY34 (GAL1-STE3 soi3), GSY36 (GAL1-STE3 soi3 pep4), GSY40 (GAL1-STE3365), and GSY41 (GAL1-STE3365 soi3). The ste3 control was GSY51. (E) Zn2+-induced constitutive endocytosis of Zrt1HAp. Zrt1-HAp expression from pMC5-HSET in strains GSY11-4D (wild-type) and GSY11-2A (soi3) was induced by 1 mM EDTA for 3 h, and turnover was initiated by adding fresh media containing 2 mM ZnCl2.(A-E) Protein turnover was monitored by immunoblotting by using anti-HA (12CA5) and affinity-purified anti-Ste3p antibodies.

Ligand-dependent turnover of Ste3365p occurs, after a lag, with a t_1/2 of 80 min (Chen and Davis, 2000). Ligand-induced turnover was only slightly slower in the mutant background, as evident by the persistence of a higher level of receptor in the mutant at 2 h after addition of a-factor (Figure 5B). Kinetics of ligand-induced internalization of the truncated receptor, as measured by protease shaving, however, were indistinguishable in the wild-type and soi3 strains (Figure 5C). Finally, kinetics of receptor recycling, as measured by sensitivity of receptor to external protease at times after removal of a-factor, were indistinguishable in the wild-type and mutant strains (Figure 5D). The fact that ligand-induced internalization and recycling rates were unchanged but that the overall rate of degradation of Ste3365p was slowed suggests that transport from an endocytic compartment to the vacuole is delayed in the soi3 mutant strain.

The soi3 Mutant Is Not Defective in Zn²⁺-induced Vacuolar Degradation of Zrt1p
To extend the analysis of loss of Soi3p function to other internalization events, we examined the Zn²⁺-induced internalization of the high-affinity Zn²⁺ transporter Zrt1p (Gitan et al., 1998; Gitan and Eide, 2000). Expression of Zrt1p was extremely low in the soi3 strain relative to wild-type (data not shown). We hypothesized that soi3 strains have a higher constitutive concentration of free Zn²⁺ in the cytosol, resulting in repression of Zrt1p synthesis (Bird et al., 2000). To express Zrt1p in soi3 and wild-type strains at comparable levels, cells expressing an epitope-tagged form of Zrt1p (Zrt1-HAp) under the ZRT1 promoter were grown in the presence of 1 mM EDTA for 3 h to lower Zn²⁺ availability and induce synthesis of Zrt1-HAp. ZnCl₂ was then added to 2 mM to shut off expression of ZRT1-HA and initiate down-regulation of the transporter (Gitan et al., 1998). In contrast to the results observed with Ste3p, rates of degradation of Zrt1-HAp were identical in the wild-type and soi3 cells (Figure 5E).

Soi3p Is a Peripheral Membrane Protein Associated with a High-density Membrane Compartment
Soi3p was tagged at the C-terminus with a triple HA-epitope tag (Soi3-HA3p). Differential centrifugation of crude lysates established that the protein was distributed between a soluble form and a form that sedimented at 200,000 x g (Figure 6A). The distribution between soluble and membrane-bound pools varied from experiment to experiment. The sedimentable form was released into the soluble fraction by treatment with 1.0 M NaCl, consistent with the behavior of Soi3p as a peripheral membrane protein (Figure 6A). When membranes containing Soi3-HA3p were subjected to sucrose equilibrium density gradient fractionation, Soi3-HA3p was found in high-density fractions (Figure 6B). The distribution of Soi3-HA3p was distinct from that of the Golgi GDPase, the PVC t-SNARE Pep12p, and the bulk of the TGN-marker protein Kex2p (Sipos and Fuller, 2002), although each of these proteins was present in small amounts in the dense fractions containing Soi3-HA3p (Figure 6B). Soi1p/Vps13p, also a peripheral membrane protein, labeled with the same epitope tag, also fractionated in a broader distribution than Soi3-HA3p (Figure 6B), consistent with proposed roles at the TGN and PVC (Brickner and Fuller, 1997). The high density of Soi3p membranes is suggestive of early endocytic membranes, because studies of -factor internalization demonstrated a higher density for early versus late endocytic carriers (Singer-Kruger et al., 1993). Additionally, Soi3p cofractionated with the dense fraction of Chs3p, which is thought to reside in early endosomal membranes (Figure 6B) (Valdivia et al., 2002). These results suggest that Soi3p associates with early endosomes rather than TGN or late endosomes. Despite the fact that a fraction of Soi3-HA3p associates with membranes, as shown by sucrose gradient fractionation, the protein still sedimented in the P200 fraction in the presence of 1% Triton X-100 (Figure 6A). This, together with the fact that 1.0 M NaCl completely extracted the protein from the P200, implies that Soi3-HA3p that sediments in the P200 fraction represents a membrane-associated high-molecular weight, salt-sensitive complex. Consistent with the association of a fraction of Soi3p with a membrane compartment, Soi3-GFP exhibited a punctate pattern of fluorescence superimposed on a diffuse, cytosolic background (Figure 6C). Seol et al. (2001) previously detected only a diffuse, cytosolic distribution of Rav1p. The faint punctate pattern seen in Figure 6C has been enhanced by image deconvolution (see MATERIALS AND METHODS), but it is observable without such enhancement. It is possible that some Soi3p may be associated with PVC membranes; however, consistent with localization of Soi3p to the early endosome rather than the PVC, we found that the pattern of Soi3-GFP localization was not altered by a class E vps mutation (vps27), which typically causes late endosomal proteins to collapse to a single "class E spot" (our unpublished data) (Piper et al., 1995).

View larger version (49K): [in this window] [in a new window]   Figure 6. Localization of Soi3p by subcellular fractionation and fluorescence microscopy. (A) Spheroplast lysate of GSY11-2A expressing Soi3HAp from its own promoter on plasmid pSOI3-HA was fractionated as described in MATERIALS AND METHODS. Soi3HAp and Pep12p were probed by immunoblotting. (B) Spheroplast lysates were subjected to sucrose gradient fractionation as described in MATERIALS AND METHODS, and aliquots were tested for the distribution of Soi3HAp, Soi1Hap, and for Golgi and endosomal markers by immunoblotting and for the distribution of Kex2 proteolytic activity (Sipos and Fuller, 2002). Soi3HAp and all other markers except Soi1HAp were analyzed by fractionating lysates of GSY11-2A expressing Soi3HAp from the ADH promoter on plasmid p413ADH-SOI3-HA. Soi1HAp fractionation was followed in lysates from JBY142. (C) GSY11-1A cells (soi3) containing control plasmid p413ADH-SOI3 (left) or p413ADH-SOI3-GFP (right) were examined by fluorescence microscopy and image deconvolution. Z-stacks of logarithmically grown cells were captured and processed using ISEE deconvolution software to enhance the punctate signal. In the right panel, arrowheads point to punctate structures that occur against a background of cytosolic Soi3-GFP fluorescence. The left panel shows an identical exposure of the control strain. Image deconvolution of Z-stacks of cells expressing soluble GFP under ADH promoter control revealed no punctate structures (our unpublished data).

The soi3 Strain Is Not Defective for Vacuolar Transport of proCPY, proALP, or proAPI
Whereas soi1 mutants exhibited a vacuolar protein sorting (Vps^-) defect (SOI1 is allelic with VPS13) (Brickner and Fuller, 1997), neither soi3-1 nor soi3 cells exhibited a Vps^- phenotype as judged by a colony-immunoblotting assay (Figure 7A). To determine whether loss of Soi3p function led to any discernible defect in delivery of newly synthesized proteins to the vacuole, cells were pulse-labeled with ³⁵S-amino acids and chased for various times. Lysates were subjected to immunoprecipitation with anti-carboxypeptidase Y antibodies to assess the Vps10p-dependent vacuolar transport pathway (Stevens et al., 1982; Klionsky and Emr, 1989), anti-ALP antibodies to assess the AP3-dependent pathway (Klionsky and Emr, 1989), and anti-API antibodies to assess the cytosol-to-vacuole (CVT) pathway (Klionsky et al., 1992). No difference was observed between the wild-type and soi3 mutant strains in the rate of delivery of proCPY to the vacuole, as judged by the rate of conversion of the Golgi form of proCPY (p2-CPY) to the mature form (m-CPY form; Figure 7B). Similarly, no alteration in the rate of delivery of proALP to the vacuole was observed in the soi3 mutant (Figure 7C). These results demonstrate that Soi3p does not play an essential role in either the Vps10p-dependent or AP3-dependent pathways from the Golgi to the vacuole. Finally, the rate of Ape1p maturation also was unaltered by the soi3 mutation (Figure 7D), indicating that the CVT pathway functions normally in the absence of Soi3p.

View larger version (52K): [in this window] [in a new window]   Figure 7. Mutation of SOI3 does not affect the CPY, ALP, or CVT pathways. (A) Vacuolar protein sorting defects were assayed by detecting secreted vacuolar protease CPY. Cells were grown on a nitrocellulose filter on a YPAD plate for 2 d, and the filters washed and immunoblotted for secreted CPY. Strains were GSY19 (vps10), JBY135-1A (soi1), GSY11-2A (soi3), SPB400-3D (soi3-1), and GSY11-4D (wild type). (B-D) Kinetics of processing of proCPY (B), proALP (C), and proAPI (D) in wild-type (GSY11-4D) and soi3 (GSY11-2A) cells were determined by 35S pulse-chase/immunoprecipitation as described in MATERIALS AND METHODS.

Soi3p Functions Upstream from the Class E/PVC Compartment
The soi3-1 mutation was isolated because it suppressed the effects of the Y₇₁₃A mutation in the TLS1 of Kex2p as measured by the efficiency of localization of the enzyme to the pro--factor processing compartment (Redding et al., 1996a). The soi3-1 mutation was classified as an allele-specific suppressor in that it suppressed the effects of the Y₇₁₃A mutation in TLS1 but not the effects of a complete deletion of the cytosolic tail (Redding et al., 1996a). The soi3-1 mutation also suppressed the effects of the F₈₅A mutation within the TGN localization signal in the N-terminal cytosolic tail of the Ste13p DPAPase A-ALP (Nothwehr et al., 1993; Redding et al., 1996a), suggesting that Soi3p function affects multiple TGN transmembrane proteins (Redding et al., 1996a).

These results suggested that the soi3-1 mutation might suppress the effects of TLS1 mutations by restoring retrieval of TLS1 mutant proteins from the late endosome. However, the effects of soi3 mutations on endocytic delivery to the vacuole and the fractionation properties of Soi3-HA3p suggested the alternative possibility that Soi3p governs the sorting of Kex2p and Ste13p through an early endosomal compartment. If this were so, Soi3p should function upstream of the late endosome, a role that could be tested by examining the epistasis of soi3 and a class E vps mutation. The class E vps mutation vps27 interferes with the function of the late endosome, blocking both transport to the vacuole and retrieval to the TGN (Piper et al., 1995). Vacuolar proteases become active in the aberrant late endosome, resulting in the degradation of TGN membrane proteins that cycle through that compartment. Mutations in TLS1 do not alter the half-life of Kex2p or A-ALP in a class E vps mutant strain, consistent with the function of TLS1 in retrieval from the late endosome (Brickner and Fuller, 1997; Bryant and Stevens, 1997). In contrast, the presence of TLS2 was found to delay degradation of Kex2p and Ste13p in such a strain, consistent with it acting upstream from the late endosome, formally as a "TGN retention" signal (Brickner and Fuller, 1997; Bryant and Stevens, 1997).

To test epistasis of soi3 and vps27, vps27 and vps27 soi3 strains were transformed with a CEN plasmid encoding a form of Kex2p, I718-tail-Kex2p, which contains TLS1 but not TLS2 (Brickner and Fuller, 1997). Pulse-chase immunoprecipitation demonstrated that whereas I718tail-Kex2p turned over rapidly (t_1/2 18 min; Table 2) in the vps27 strain (Figure 8A), the protein was stabilized in the vps27 soi3 double mutant (t_1/2 62 min; Figure 8A and Table 2). Y₇₁₃A-Kex2p, which has TLS2 but lacks TLS1, turned over more slowly in the vps27 strain (t_1/2 39 min; Table 2) but was still stabilized in the double mutant (t_1/2 93 min; Table 2). The soi3 mutation also delayed delivery of WT Kex2p to the class E compartment in the vps27 background (Table 2). These data argue strongly that the effect of the soi3 mutation on Kex2p occurs upstream from the late endosome.

View larger version (30K): [in this window] [in a new window]   Figure 8. Deletion of SOI3 prevents the rapid turnover of I718Kex2p in vps27 cells. EBY22 (soi3 kex2 vps27) cells carrying pCWKX10-I718 and either pRS413ADH-SOI3 (vps27) or pRS413ADH (vps27 soi3) were subjected to 35S pulse-chase/immunoprecipitation as described in MATERIALS AND METHODS. Vps10* refers to the clipped form of Vps10p produced by proteolysis of Vps10p by activated vacuolar proteases in the class E PVC compartment (Bryant and Stevens, 1997). Anti-lumenal antiserum was used for IP of I718Kex2p.

Vps10p Endosomal Cycling Does Not Require Soi3p
The observation that proCPY sorting was not affected by loss of Soi3p function implied that the soi3 mutation should not affect cycling of the Vps10p receptor. This was confirmed by examining the fate of Vps10p by pulse-chase/immunoprecipitation in vps27 and vps27 soi3 strains. Vps10p undergoes proteolytic clipping when delivered to the aberrant late endosome in a vps27 strain (Figure 8B) (Bryant and Stevens, 1997). In contrast to the stabilization of Kex2p, the rate and extent of proteolytic clipping of Vps10p were not altered by the soi3 mutation (Figure 8B). These results rule out the possibility that the soi3 merely abrogates proteolytic activity in the class E compartment, because proteolytic cleavage of Vps10p was identical in the vps27 and vps27 soi3 strains. Therefore, we conclude that loss of Soi3p function interferes with a pathway traveled by Kex2p and not by Vps10p.

soi3 and soi3-1 Have Different Effects on Wild-Type, Y₇₁₃A, and C-tail-Kex2p
The soi3-1 mutation was classified as an allele-specific suppressor of the Y₇₁₃A mutation in the Kex2p cytosolic tail because it failed to suppress, in the onset of impotence assay, the effects of either the complete deletion of the tail (C-tail) or deletion of roughly 30 residues in the membrane proximal portion of the tail that removed TLS1 (Redding et al., 1996a). The soi3-1 mutation lengthened the half-life of both wild-type and Y₇₁₃A Kex2p and was shown to be recessive for its effect on the half-life of Y₇₁₃A Kex2p (Redding et al., 1996a). Surprisingly, the soi3 mutation had distinct effects. First, the deletion mutation suppressed both the Y₇₁₃A and C-tail mutations in the onset of impotence assay (Figure 9, top, top and bottom rows). Both the soi3-1 and soi3 mutations suppressed the Y₇₁₃A mutation in the absence of TLS2; that is, the Y₇₁₃A, I718tail-Kex2p was indistinguishable from Y₇₁₃AKex2p in this assay (Figure 9, top, middle rows). In addition, whereas the soi3-1 mutation had no obvious effect on wild-type Kex2p, the soi3 mutation had a negative effect on the persistence of the wild-type enzyme in the pro--factor processing compartment as judged by the onset of impotence assay (Figure 9, bottom, top two rows). This effect was not seen with I718tail Kex2p, which possesses TLS1 but lacks TLS2 (Figure 9, bottom, bottom two rows).

View larger version (96K): [in this window] [in a new window]   Figure 9. soi3 and soi3-1 exert different effects in the onset of impotence assay. Strains KRY18-1A (SOI3), SPB400-3D (soi3-1) and GSY11-7A (soi3) carrying plasmids pCWKX21 (GAL-KEX2 Y713A), pCWKX21-I718 (GAL-KEX2 Y713A I718tail), pCWKX27 (GAL-KEX2 C-tail), pCWKX20 (GAL-KEX2), pCWKX20-I718tail (GAL-KEX2 I718tail) were shifted from galactose to glucose medium for the indicated times and assessed for mating competence as described (Redding et al., 1996a).

Pulse-chase analysis confirmed these observations (Figure 10; data summarized in Table 2). Whereas the soi3-1 mutation slowed vacuolar turnover of wild-type Kex2p, the soi3 mutation accelerated it (Figure 10A and Table 2). In contrast, the soi3 slightly delayed transport of I718tail-Kex2p to the vacuole (Table 2). Both the soi3-1 and soi3 mutations delayed vacuolar turnover of Y₇₁₃A-Kex2p (Figure 10B and Table 2). In agreement with the onset of impotence data, the soi3 delayed the vacuolar turnover of C-tail-Kex2p, but the soi3-1 mutation had no effect (Figure 10C and Table 2). Consistent with the different effects of soi3-1 and soi3 mutations, soi3-1 was found to correspond to a single nucleotide change (G to A at position 350 in the structural gene), resulting in substitution of Glu for Gly₁₁₈ (our unpublished data).

View larger version (32K): [in this window] [in a new window]   Figure 10. Effects of the soi3 mutants on the turnover of C-tail mutant forms of Kex2p. GSY11-2A (soi3), SPB400-3D (soi3-1), and GSY11-4D (wild type) cells carrying plasmids (A) pCWKX10 (WT Kex2p), (B) pCWKX11 (Y713A-Kex2p), or (C) pCWKX17 (C-tail-Kex2p) were subjected to 35S pulse-chase/immunoprecipitation as described in MATERIALS AND METHODS. Anti-C-tail antiserum was used for IP of wild-type Kex2p and Y713A-Kex2p, and anti-lumenal antiserum was used for IP of C-tail-Kex2p.

SOI3 and VPS1 Govern Distinct Pathways to the Vacuole
The effect of the soi3 on endocytic cargo seemed to be selective, in that delivery of Ste3p to the vacuole was delayed but delivery of Zrt1p was not. In addition, loss of Soi3p did not completely block vacuolar delivery of either FM4-64 or Ste3p, suggesting the existence of one or more bypass pathways. One possible bypass pathway would be from the early endosome to the TGN and thence to the PVC. The difference between Ste3p and Zrt1p in the soi3 background might be due to transport of Zrt1p via such a pathway. In this case, mutation of VPS1, which is required for TGN to PVC transport (Wilsbach and Payne, 1993; Nothwehr et al., 1995) would be expected to interfere with endocytic transport of Zrt1p to the vacuole. When VPS1 was deleted in a soi3/SOI3 heterozygous diploid and in a soi3/soi3 homozygous diploid, tetrad analysis demonstrated synthetic lethality between vps1 and soi3 (our unpublished data). To determine the effect of loss of VPS1 function on Zrt1p and Ste3p in a soi3 background, a strain was constructed that contained a temperature-sensitive allele of VPS1 and the soi3. When down-regulation of Zrt1HAp was induced by Zn²⁺ addition, vacuolar degradation of the protein was delayed in the vps1-ts strain relative to the wild-type strain even at the permissive temperature of 26°C (Figure 11A). Zrt1HAp degradation was accelerated in the wild-type strain at 37°C relative to 26°C (Figure 11A). In contrast, the presence of the vps1-ts allele strongly stabilized Zrt1HAp at 37°C (nonpermissive temperature the vps1-ts allele), and addition of the soi3 mutation did not augment this effect (Figure 11A). Ste3HAp behaved in the opposite manner. Although deletion of SOI3 clearly stabilized Ste3HAp in the vps1-ts background both at 26 and 37°C, the vps1-ts mutation had no effect on the constitutive rate of Ste3HAp turnover in either the SOI3 or soi3 background at either temperature (Figure 11B). Thus, whereas Zn²⁺-induced down-regulation and vacuolar degradation of Zrt1HAp was Vps1p dependent and Soi3p independent, constitutive endocytic degradation of Ste3HAp was Soi3p dependent and Vps1p independent.

View larger version (23K): [in this window] [in a new window]   Figure 11. Differential effects of soi3 and vps1-ts mutations on Zrt1HAp and Ste3HAp. Zrt1HAp (A) and Ste3HAp (B) were expressed in wild-type (GSY11-4D), vps1-100-ts (EBY77-4) and soi3 vps1-100-ts (EBY77-8) cells. Zrt1HAp turnover was initiated as described in MATERIALS AND METHODS. Ste3HAp was induced from the GAL1 promoter on galactose media, and its expression was turned off by the addition of glucose. Both proteins were induced in cells growing at 26°C. Cells were then harvested, and aliquots were diluted with fresh media prewarmed either to 26 or 37°C. Protein turnover was followed by immunoblotting.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION ACKNOWLEDGMENTS REFERENCES

 
Soi3p Function Is Required for Early Endosome-to-PVC Transport
SOI3 was identified by a recessive allele, soi3-1, that suppressed vacuolar mislocalization of Y₇₁₃A-Kex2p as well as mutation of the TGN retrieval signal in the Ste13p cytosolic tail (Redding et al., 1996a). Unlike mutations in SOI1/VPS13 (Brickner and Fuller, 1997), soi3 mutations suppressed the Y₇₁₃A mutation in the absence of the TGN retention signal TLS2 (Figure 1B). The fact that the soi3 mutations were recessive and had no defect in vacuolar protein sorting suggested that loss of Soi3p either improved retrieval of TLS1-mutant forms of Kex2p and Ste13p from the PVC or that a novel mechanism was at work.

The evidence presented here argues for a novel mechanism, that Soi3p functions at the early endosome and is important for transport of both endocytic cargo and TGN transmembrane proteins from the early endosome to the PVC. First, soi3 mutants exhibit a kinetic delay in delivery of FM4-64 to the vacuole, with the delay occurring in transport between the 14°C endocytic intermediate compartment and the vacuole. Consistent with the persistence of FM4-64 staining in punctate structures in the soi3 mutant, we observed accumulation of fenestrated, tubular membrane structures in the soi3-1 mutant by EM. Second, the rate of constitutive vacuolar turnover of the Ste3p a-factor receptor was substantially decreased in the soi3 mutant, whereas rates of internalization and recycling of Ste3p were unaltered. Third, membrane-associated Soi3p cofractionated with Chs3p in a dense fraction characteristic of early endosomes. Consistent with early endosome localization, a fraction of Soi3-GFP localized in a peripheral, punctate pattern. Fourth, soi3 mutations delayed delivery of Y₇₁₃A-Kex2p, but not Vps10p, to the class E (aberrant PVC) compartment. The Vps10p-dependent, AP3-dependent, and CVT vacuolar targeting pathways were unaffected by loss of Soi3p. Each of these pathways is likely to require normal TGN functioning, including the CVT pathway, which depends on the TGN SNAREs Tlg1p and Tlg2p (Reggiori et al., 2003). Finally, the synthetic lethality of soi3 with vps1, by itself, is consistent with Soi3p having a role in endocytotic transport to the vacuole, given the synthetic lethality of vps1 with end4 mutations (Nothwehr et al., 1995; Conibear and Stevens, 2000). Together, these data argue strongly for Soi3p function in early endosome to PVC transport. We should emphasize here, however, that we cannot rule out, on the basis of these data, roles for Soi3p in other transport steps, in particular between the PVC and the vacuole.

The soi3 null mutation only partially blocked FM4-64 trafficking to the vacuole and endocytic degradation of Ste3p, but such partial effects are in line with the effects of other mutants shown to affect vacuolar delivery of FM4-64 and Ste3p (Gerrard et al., 2000; Heese-Peck et al., 2002; Shaw et al., 2003). The partial block may be due to the existence of a bypass pathway, but the fact that the delayed vacuolar delivery of Ste3p (Figure 11B) and FM4-64 (our unpublished data) was not further impaired by a vps1-ts mutation argues against transport of Ste3p and FM4-64 to the vacuole via the TGN-PVC pathway. The bypass pathway might instead correspond to direct fusion of early endosomes with the vacuole, a phenomenon suggested by EM analysis of the soi3-1 mutant (Figure 3B). In contrast, the vps1-ts mutation did and the soi3 did not affect endocytic degradation of Zrt1p (Figures 5E and 11A), suggesting that Ste3p and Zrt1p follow different pathways to the vacuole.

Zinc Sensitivity of soi3 Mutants
Zn²⁺ hypersensitivity of the soi3 mutants initially led us to examine endocytosis of Zrt1p. However, although we found that vacuolar delivery of Zrt1p induced by Zn²⁺ was unaltered in the soi3 mutant, expression of Zrt1p was markedly reduced in growth in standard synthetic growth medium (our unpublished data), suggesting that soi3 mutations disrupt Zn²⁺ homeostasis, leading to higher cytosolic Zn²⁺ levels. The possibility that soi3 mutants are defective in Zn²⁺ sequestration in the vacuole is supported by the finding that ZRC1, which encodes a Zn²⁺ transporter in the vacuolar membrane (MacDiarmid et al., 2002), was isolated as a double-copy suppressor in the initial cloning of the soi3-1 mutation by complementation of the Zn²⁺-hypersensitive phenotype (clones 1 and 30 in Figure 2A; other data not shown).

Kex2p and Ste13p Cycle through the Early Endosome
Evidence presented here that Soi3p functions at the early endosome along with the effects of soi3 mutations on Y₇₁₃AKex2p and F₈₅A-A-ALP (Redding et al., 1996a) argue that both Kex2p and A-ALP (as surrogate for Ste13p) cycle through the early endosome. Other studies support this. First, Kex2p partially colocalizes with Chs5p, which in turn colocalizes with Chs3p, a protein whose localization to an internal punctate organelle termed the chitosome requires endocytosis (Santos and Snyder, 1997; Ziman et al., 1998). Second, localization of Kex2p to an early or recycling endosome also was suggested by colocalization of Kex2p with GFP-labeled Snc1p, the v-SNARE of secretory vesicles, to punctate internal sites presumed to be intermediates in the recycling of Snc1p from the plasma membrane to the TGN (Lewis et al., 2000; Ha et al., 2001). Third, mutations in INP53, which encodes a synaptojanin homolog, interfered with the function of the TLS2-like signal in A-ALP (Ha et al., 2001). Mutation of INP53 accelerated vacuolar delivery not only of F₈₅A-A-ALP but also of Kex2p without affecting Vps10p. Like mutations in the subunit of the clathrin adaptor complex AP-1, inp53 mutations were found to result in synthetic growth defects when combined with double mutations in GGA1 and GGA2, leading to the suggestion that Inp53p and AP-1 were required for a TLS2-dependent transport pathway between the TGN and early endosome (Ha et al., 2003). Whereas, inp53 mutations increased the rate of vacuolar delivery of TLS1^- TLS2⁺ forms of Kex2p and A-ALP (Y₇₁₃A-Kex2p and F₈₅A-A-ALP), soi3 mutations decreased the rate of transit to the vacuole of the TLS1^- TLS2⁺ proteins. This can be understood if Inp53p (and AP-1) function in delivery of Ste13p and Kex2p to the early endosome and Soi3p functions in transport from the early endosome to the PVC.

Partitioning of Kex2p between Two TGN-PVC Pathways
The effects of soi3 mutations on Kex2p argue that Kex2p can follow a pathway from the TGN through the early endosome to the PVC. However, the dramatic effects of vps1 mutations on Kex2p localization (Wilsbach and Payne, 1993; Nothwehr et al., 1995) argue that Kex2p also partitions into the direct route between the TGN and PVC that