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Originally published In Press as doi:10.1074/jbc.M611345200 on April 11, 2007

J. Biol. Chem., Vol. 282, Issue 23, 16736-16743, June 8, 2007
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Phosphatidylethanolamine, a Limiting Factor of Autophagy in Yeast Strains Bearing a Defect in the Carboxypeptidase Y Pathway of Vacuolar Targeting*

Ruth Nebauer, Sabine Rosenberger, and Günther Daum1

From the Institute of Biochemistry, Graz University of Technology, Petersgasse 12/2, A-8010 Graz, Austria

Received for publication, December 11, 2006 , and in revised form, March 30, 2007.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
 REFERENCES
 
Vps4p and Vps36p of Saccharomyces cerevisiae are involved in the transport of proteins to the vacuole via the carboxypeptidase Y pathway. We found that deletion of VPS4 and VPS36 caused impaired maturation of the vacuolar proaminopeptidase I (pAPI) via autophagy or the cytosol to vacuole targeting pathway. Supplementation with ethanolamine rescued this defect, leading to an increase of the cellular amount of phosphatidylethanolamine (PtdEtn), an enhanced level of the PtdEtn-binding autophagy protein Atg8p and a balanced rate of autophagy. We also discovered that maturation of pAPI was generally affected by PtdEtn depletion in a psd1{Delta} psd2{Delta} mutant due to reduced recruitment of Atg8p to the preautophagosomal structure. Ethanolamine supplementation provided the necessary amounts of PtdEtn for complete maturation of pAPI. Since the expression level of Atg8p was not compromised in the psd1{Delta} psd2{Delta} strain, we concluded that the amount of available PtdEtn was limiting. Thus, PtdEtn appears to be a limiting factor for the balance of the carboxypeptidase Y pathway and autophagy/the cytosol to vacuole targeting pathway in the yeast.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
 REFERENCES
 
Phosphatidylethanolamine (PtdEtn)2 is essential for growth of the yeast Saccharomyces cerevisiae and required for function and integrity of mitochondrial membranes (1). PtdEtn can be synthesized by three different pathways, namely through decarboxylation of phosphatidylserine (PtdSer) by the major phosphatidylserine decarboxylase, Psd1p, a component of the inner mitochondrial membrane; through extramitochondrial decarboxylation of PtdSer by Psd2p; and through the CDP-ethanolamine branch of the Kennedy pathway (for a recent review, see Ref. 2). A lack of the major PtdEtn-synthesizing enzyme, Psd1p, leads to a substantial decrease of PtdEtn in total cellular and mitochondrial membranes, thereby conferring a petite phenotype, which is linked to the loss of respiratory capacity (1). Moreover, depletion of PtdEtn causes defects in the assembly of mitochondrial protein complexes and loss of mitochondrial DNA (1, 3, 4). PtdEtn also plays a crucial role in glycosylphosphatidylinositol anchor biosynthesis (5).

In Saccharomyces cerevisiae, PtdEtn was also shown to be involved in two vacuolar delivery pathways, autophagy and cytosol to vacuole targeting (Cvt) (see Fig. 1) (reviewed in Refs. 6–8). These processes are mechanistically related and involve the formation of double-membrane cytosolic vesicles, sequestering either precursor aminopeptidase I (pAPI) specifically or, in the case of autophagy, also enveloping bulk cytosol in a non-selective manner. Whereas autophagy is a catabolic process inducible by starvation, the Cvt pathway is a constitutive biosynthetic route. PtdEtn dependence of autophagy/the Cvt pathway is due to covalent binding of the phospholipid to the starvation-inducible autophagy protein Atg8p (9–11). Lipid modification of the polypeptide is mediated by a ubiquitin-like system and essential for localization of Atg8p to the preautophagosomal structure (PAS) (10, 12). Atg8p is then delivered to the vacuole enclosed in double-membrane transport vesicles and finally turned over by vacuolar proteases. Involvement of Atg8p as a structural component in vesicle formation was suggested.

The main pathway for the delivery of newly synthesized proteins to the vacuole is the carboxypeptidase Y (CPY) pathway (13). The CPY pathway involves transport of proteins from the late Golgi complex via a prevacuolar compartment (PVC) to the vacuole. A second pathway, referred to as the alkaline phosphatase pathway (13), differs from the CPY pathway insofar as it uses a different type of Golgi-derived carrier vesicles and bypasses the PVC en route to the vacuole.

Vps4p and Vps36p are two polypeptides that are involved in the transport of CPY precursors to the vacuole (14–16). Vps4p is required for protein translocation from early to late endosomes (17) and may also play a role in the supply of phospholipids to different compartments (18). VPS4 is a class E VPS gene that encodes a protein that belongs to the family of AAA type ATPases. Class E vps mutants accumulate vacuolar, endocytic, and late Golgi markers in an aberrant multilamellar structure, the so-called class E compartment (19). Internalization of proteins in the PVC occurs in concerted action of the three multisubunit complexes ESCRT-I, -II, and -III (15), which are proposed to act sequentially in the order I, II, and III to select and concentrate cargoes destined for internalization in the multivesicular body/CPY pathway. Loss of Vps4p activity results in the accumulation of ESCRT-III components on the membrane (20), suggesting a role for Vps4p in disassembly of complexes on the PVC membrane during cargo sorting. Deletion of a class E VPS gene, however, does not lead to a complete block in protein and membrane transport to the vacuole. In this case, translocation of polypeptides may occur by alternative mechanisms that are different from the normal endosome to vacuole transport system.


Figure 1
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  		FIGURE 1.
PtdEtn dependence of protein delivery pathways to the vacuole. In the Cvt pathway, cytoplasmic proteins, such as oligomerized precursor aminopeptidase I, are internalized within a double membrane Cvt vesicle. Cvt vesicles then fuse with and deliver their material into the vacuole. In autophagy, cytoplasmic proteins are enclosed in a double membrane autophagosome, which fuses with the vacuole to release membranes and cargo for degradation. This pathway is similar to Cvt but used primarily under starvation conditions. The CPY pathway sorts newly synthesized proteins from the late Golgi to late endosomes/multivesicular bodies (MVB)/prevacuolar compartment (PVC).

 
In the study presented here, we aimed at identifying components that were affected by changes in the cellular PtdEtn level. A genetic screening led to the identification of mutants defective in Vps4p and Vps36p. When the CPY route is inactivated by vps4 or vps36 mutations, autophagy/the Cvt pathway is also impaired. We demonstrate that full activity of the latter route requires a certain cellular level of PtdEtn, which is essential for the formation of autophagosomes/Cvt vesicles by covalently binding to Atg8p. The general requirement for PtdEtn in the targeting of proteins to the vacuole is discussed.


   EXPERIMENTAL PROCEDURES
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
RESULTS
 DISCUSSION
 REFERENCES
 
Strains and Culture Conditions—Yeast strains and plasmids used in this study are listed in Table 1. S. cerevisiae strains were grown under aerobic conditions at 30 or 37 °C on synthetic minimal medium containing 2% glucose (SD) or 2% lactate (SL), respectively, or on YP medium (1% yeast extract and 2% peptone) containing 2% glucose (YPD) or lactate (YPL), respectively, as the carbon source. In the cases indicated, supplementation with serine, ethanolamine, or choline was 2 mM. Starvation medium consisted of 0.17% yeast nitrogen base without amino acids and without ammonium sulfate and 2% glucose (SD(–N)) or 2% lactate (SL(–N)). For large scale cultivation, inoculations to an A600 of 0.1 in fresh medium were made by diluting precultures grown to the stationary phase. For auxotrophy tests, yeast strains were cultivated on solid synthetic medium (21).


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  		TABLE 1
Yeast strains and plasmids used in this study

 
Primers used in this study are listed in Table 2. Primers PSD2-F1 and PSD2-R1 were used to amplify the His3MX6 disruption cassette (22), which was introduced into vps4{Delta} and vps36{Delta} by lithium acetate transformation (23). Correct insertion of the cassette was tested by growth on selective medium without the respective amino acid and by colony PCR with the appropriate primers.


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  		TABLE 2
Primers used in this study

 
Transposon Mutagenesis Screening—The S. cerevisiae strain YRB3 (see Table 1) was transformed with a transposon-based knock-out library (24). Approximately 100,000 transformants were screened for ethanolamine auxotrophy on glucose minimal medium at 37 °C. The site of transposon insertion was identified using a vectorette PCR protocol as described (available on the World Wide Web at genome-www.stanford.edu/group/botlab/protocols/vectorette.html) employing the oligonucleotides Bubble-1, -2, and -224 (Table 2). DNA sequencing was performed at MWG Biotech AG (Ebersberg, Germany).

Analysis of Strains Bearing a GFP-Atg8p Hybrid—Cells expressing the centromeric plasmid GFP-Atg8p, which carries a GFP-Atg8p fusion under the native Atg8p promoter (kindly provided by Y. Ohsumi, Okazaki, Japan), were grown on SD or SL medium to the late exponential phase, harvested, washed twice with water, and then shaken at 30 °C in SD(–N) or SL(–N) medium. Samples were taken within a time range of 4 h and subjected to alkaline lysis (25). Western blot analysis was performed as described below.

Wild type and psd1{Delta} psd2{Delta} cells expressing GFP-Atg8p were grown to the late logarithmic growth phase on SL medium supplemented with Etn and shifted to SL(–N) supplemented with Etn for 4 h. Cells were screened under the fluorescence microscope, and cells with fluorescence signals on the PAS were counted. As controls, atg1{Delta} and atg21{Delta} cells expressing GFP-Atg8p were analyzed under the microscope. Fluorescence and light microscopy was performed using a Zeiss Axiovert 35 microscope.

Western Blot Analysis—Proteins were quantified by the method of Lowry (26). SDS-polyacrylamide gel electrophoresis of polypeptides from cell homogenates prepared by glass beading as described below or from homogenates obtained by alkaline lysis (25) was carried out by the method of Laemmli et al. (27). Western blot analysis was performed as described by Haid and Suissa (28) using a primary rabbit antibody against pAPI or Atg8p (kindly provided by M. Thumm, Göttingen, Germany) or a primary mouse antibody against GFP (Roche Applied Science). Immunoreactive bands were visualized by enzyme-linked immunosorbent assay using a peroxidase- or alkaline phosphatase-linked secondary antibody (Sigma) following the manufacturer's instructions.

Phospholipid Analysis—For the analysis of total cellular phospholipids, yeast cells harvested from a 500-ml culture grown to the late logarithmic phase were disintegrated by shaking with glass beads in a Merckenschlager homogenizer under CO2 cooling in the presence of 10 mM Tris/HCl, pH 7.2, and 1 mM phenylmethylsulfonyl fluoride (Calbiochem). After removal of the beads by centrifugation, the supernatant representing the total cell homogenate was aliquoted and stored at –70 °C. Lipids from samples containing 3 mg of protein were extracted by the procedure of Folch et al. (29) using 4 ml of chloroform/methanol (2:1, v/v).

Individual phospholipids were separated by two-dimensional thin layer chromatography (TLC) using chloroform/methanol/25% ammonia (70:35:5, v/v/v) as first and chloroform/acetone/methanol/acetic acid/water (55:20:10:10:5, v/v/v/v/v) as second developing solvent. Phospholipids were visualized on TLC plates by staining with iodine vapor, scraped off, and quantified by the method of Broekhuyse (30).


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
DISCUSSION
 REFERENCES
 
A Screen for Mutants with an Enhanced Requirement for Phosphatidylethanolamine Identifies vps4 and vps36—To investigate the function of PtdEtn in yeast cells and to identify processes that depend on PtdEtn, we performed a screening for mutants that require exogenous ethanolamine as a supplement when cellular PtdEtn homeostasis is disturbed. To increase the stringency of this screening, we used a psd2{Delta} genetic background. The PtdEtn level of a psd2{Delta} mutant was slightly decreased as compared with wild type (Table 3) but still higher than in a psd1{Delta} strain that lacks the major cellular PtdSer decarboxylase (3). Moreover, the temperature of 37 °C was chosen as another means to modulate the PtdEtn requirement of the yeast. At this temperature, the cellular level of PtdEtn is lower than at 30 °C, which made the screening more efficient for the expected defects. Thus, an appropriate strategy had been designed to identify mutations that were sensitive to alterations of the PtdEtn amount in the cell.


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  		TABLE 3
Phospholipid composition of homogenates

Mean values of at least three independent measurements are shown. Mean deviations are less than 3%. PtdCho, phosphatidylcholine; PtdIns, phosphatidylinositol; LPL, lysophospholipids; DMPE, dimethylphosphatidylethanolamine; PA, phosphatidic acid; CL, cardiolipin.

 
For the introduction of random deletions into the genome, the psd2{Delta} deletion strain was transformed with a transposon-based knock-out library (see "Experimental Procedures"). Mutants with a requirement for ethanolamine were selected on glucose minimal medium with or without ethanolamine, respectively, at 37 °C. This approach led to the identification of 10 mutants.3 Two of these mutants contained a transposon insertion in genes that are involved in vacuolar protein sorting, namely VPS4 and VPS36. For further investigations, we used the vps4{Delta} and vps36{Delta} deletion strains (Table 1) from the Euroscarf collection (Frankfurt, Germany).


Figure 2
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  		FIGURE 2.
Etn dependence of growth of vps4{Delta} and vps36{Delta} at 37 °C (A) and at 30 °C (B). BY4742 ({blacktriangleup}), BY4742 + Etn ({circ}), vps4{Delta} (x), vps4{Delta}+ Etn (•), vps36{Delta} ({triangleup}), and vps36{Delta}+ Etn ({blacksquare}) were tested on glucose minimal medium. Supplementation with Etn was 2 mM.

 
Ethanolamine dependence of growth on glucose minimal medium at 37 °C was confirmed with vps4{Delta} psd2{Delta} and vps36{Delta} psd2{Delta} double deletion strains (data not shown). Surprisingly, vps4{Delta} and vps36{Delta} single mutants (Fig. 2A) exhibited the same ethanolamine auxotrophy as psd2{Delta} vps4{Delta} and psd2{Delta} vps36{Delta} double mutants. Thus, the ethanolamine auxotrophy was independent of psd2{Delta} and only due to deletion of VPS4 or VPS36, indicating that the vps4{Delta} and vps36{Delta} mutants had an increased requirement for PtdEtn. A similar effect, although less pronounced, was observed at 30 °C (Fig. 2B), supporting our strategy to perform the screening at 37 °C (see above).

Supplementation with Ethanolamine Increases the Amount of Phosphatidylethanolamine in vps4{Delta} and vps36{Delta} Strains—To test whether the ethanolamine auxotrophy of vps4{Delta} and vps36{Delta} was reflected in the amount of PtdEtn in the respective mutants, we analyzed homogenates of cells grown on minimal medium with or without ethanolamine (Table 3). In the absence of ethanolamine, the wild type BY4742, vps4{Delta}, and vps36{Delta} contained the same amount of PtdEtn, whereas the psd2{Delta} mutant used as a control showed a slight decrease of PtdEtn. The addition of ethanolamine to the medium generally led to an increase of the amount of PtdEtn, which was accompanied by the decrease of phosphatidylcholine in all strains that were analyzed. The increase of the PtdEtn level upon ethanolamine supplementation in vps4{Delta} and vps36{Delta} was even higher than in wild type. Thus, enhanced formation of PtdEtn by supplementation with ethanolamine in vps4{Delta} and vps36{Delta} correlated with the growth characteristics. Supplementation with serine or choline did not lead to an increased cellular level of PtdEtn (see Table 3).


Figure 3
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  		FIGURE 3.
Processing of pAPI and expression of Atg8p in BY4742, vps4{Delta}, and vps36{Delta}. Cells were grown to the end of logarithmic growth phase on glucose minimal medium with or without Etn at 37 °C and shifted to SD(–N) for 4 h. 20 µg of proteins from cell homogenates were immunoblotted with antibodies against pAPI or Atg8p.

 
Processing of Proaminopeptidase I in vps4{Delta} and vps36{Delta} Is Enhanced in the Presence of Ethanolamine—Since growth of vps4{Delta} and vps36{Delta} was improved by ethanolamine, we hypothesized that a block of the CPY pathway might cause enhancement of a vacuolar transport pathway different from autophagy and/or the Cvt pathway (see Fig. 1) and increase the requirement for PtdEtn. This hypothesis is in line with the finding of Ichimura et al. (10), who showed that PtdEtn plays a role in autophagy by covalently conjugating to Atg8p. A marker protein for autophagy/the Cvt pathway in S. cerevisiae is pAPI, a resident vacuolar proteinase, which was described to be selectively targeted to the vacuole through this route. Once in the vacuole, pAPI is proteolytically matured (6, 8).

To test the above mentioned hypothesis, we examined maturation of pAPI in vps4{Delta} and vps36{Delta} and studied the effect of ethanolamine on this process. For analysis of the effects on autophagy, cells were grown to the late exponential phase, shifted to starvation medium for 4 h, and analyzed with antibodies against pAPI (Fig. 3). In the absence of ethanolamine, maturation of pAPI was incomplete in vps4{Delta} and vps36{Delta} with ~20% of API remaining in its precursor form, whereas the addition of ethanolamine led to the same level of maturation as in wild type. Thus, maturation of pAPI in vps4{Delta} and vps36{Delta} correlated with the ethanolamine-induced growth rate. Entirely the same result was obtained for the Cvt pathway (data not shown).

To further explore the specific dependence of pAPI maturation on PtdEtn in vps4{Delta} and vps36{Delta}, we studied growth, phospholipid composition and pAPI processing upon the addition of serine and choline to the growth medium. Serine can be introduced into PtdEtn via Psd1p- or Psd2p-dependent PtdSer decarboxylation, and choline can be incorporated into phosphatidylcholine via the CDP-choline pathway (2) (reviewed in Ref. 31). Thus, an effect of serine addition on pAPI maturation could be expected, because PtdSer is the direct precursor of PtdEtn. In contrast, choline should only exert an effect similar to that of ethanolamine if the observed effects were generally due to aminoglycerophospholipid homeostasis.


Figure 4
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  		FIGURE 4.
Processing of pAPI in BY4742, vps4{Delta}, and vps36{Delta} in the presence of serine or choline (Cho) at 37 °C. Cells were grown to the end of logarithmic growth phase on glucose minimal medium with or without Ser or choline at 37 °C and shifted to SD(–N) for 4 h. 20 µg of proteins from cell homogenates were immunoblotted with antibodies against pAPI.

 
In the wild type, growth was unchanged irrespective of serine or choline supplementation. Serine improved growth of vps4{Delta} and vps36{Delta} similar to ethanolamine, but choline enhanced only growth of vps4{Delta} to a small extent (data not shown). However, serine or choline addition to the growth medium neither changed the PtdEtn level of BY4742, vps4{Delta}, or vps36{Delta} (see Table 3) nor processing of pAPI (Fig. 4). Conclusively, enhancement of maturation of pAPI to the level of wild type in vps4{Delta} and vps36{Delta} appears to be specifically due to the increased cellular level of PtdEtn caused by supplementation with exogenous ethanolamine.

Phosphatidylethanolamine Is Essential to Overcome the Autophagy Defect in vps4{Delta} and vps36{Delta}—Since PtdEtn was shown to conjugate covalently to the autophagy protein Atg8p, we examined Atg8p expression in vps4{Delta} and vps36{Delta} in the presence or absence of ethanolamine. As shown in Fig. 3, the level of Atg8p in the mutants was comparable with wild type in the absence of ethanolamine but ~3-fold increased upon the addition of ethanolamine to the medium. Thus, although vps4{Delta} and vps36{Delta} had wild type levels of PtdEtn (see Table 3) and Atg8p in the absence of ethanolamine, autophagy was defective in the mutants as shown by the maturation defect of pAPI (see Fig. 3). We speculated from these results that in vps4{Delta} and vps36{Delta}, ethanolamine supplementation and, consequently, enhanced levels of PtdEtn and Atg8p are required to increase the rate of autophagy to the wild type level. To test this hypothesis, we measured the rate of autophagy in vps4{Delta} and vps36{Delta} by following the selective vacuolar targeting of GFP-Atg8p as reported by Meiling-Wesse et al. (32). Similar to Atg8p, GFP-Atg8p is targeted to the vacuole, where proteolysis of the fusion protein leads to formation of free GFP. As opposed to unsupplemented cells, ethanolamine supplementation of vps4{Delta} indeed led to a production of free GFP comparable with wild type (see Fig. 5). Similar results were obtained with vps36{Delta} (data not shown). Thus, the requirement for autophagy and consequently for autophagosome-associated Atg8p in vps4{Delta} and vps36{Delta} can obviously only be fulfilled when a sufficient amount of PtdEtn is present for anchoring the polypeptide to the membrane.

Phosphatidylethanolamine Depletion Leads to a Processing Defect and Decreased Amounts of Proaminopeptidase I—The obvious importance of PtdEtn for autophagy led us to examine in a more general way the contribution of the different PtdEtn biosynthetic pathways (see Introduction) to the cellular pool of PtdEtn necessary for autophagy/the Cvt pathway. To study possible effects of PtdEtn depletion on pAPI maturation, we analyzed pAPI processing in wild type, psd1{Delta}, psd2{Delta}, psd1{Delta} psd2{Delta}, and cki1{Delta} dpl1{Delta} eki1{Delta}. It has to be noted that defects in the different pathways lead to a different extent of PtdEtn depletion. Although the psd2{Delta} and cki1{Delta} dpl1{Delta} eki1{Delta} mutants did not have a significantly altered PtdEtn level as compared with wild type, PtdEtn was reduced in psd1{Delta} and even more dramatically in psd1{Delta} psd2{Delta} (1).


Figure 5
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  		FIGURE 5.
The rate of autophagy in vps4{Delta} supplemented with ethanolamine is increased to wild type level. Cells expressing GFP-Atg8p from a centromeric plasmid under control of the ATG8 promoter were grown to the exponential growth phase in SD medium and starved for nitrogen in SD(–N) medium for the indicated times. Cell extracts were separated by SDS-PAGE and, after electroblotting on a nitrocellulose membrane, analyzed with an antibody against GFP.

 


Figure 6
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  		FIGURE 6.
Processing of pAPI and expression of Atg8p of FY1679, psd1{Delta}, psd2{Delta}, psd1{Delta} psd2{Delta}, and cki1{Delta} dpl1{Delta} eki1{Delta} cells grown to the stationary phase on YPL and shifted to SL(–N) for 4 h. 20 µg of proteins from cell homogenates were immunoblotted with antibodies against pAPI or Atg8p.

 
Processing of pAPI was examined in cells grown on lactate complete medium (YPL). On nonfermentable carbon sources, a higher level of PtdEtn is required for growth than on glucose-containing media, and maintaining growth of a strain deleted of PSD1 requires supplementation with ethanolamine (1). The growth rate of psd1{Delta} psd2{Delta} is dramatically reduced on YPL even in the presence of ethanolamine and choline in YP media, and the PtdEtn level of psd1{Delta} psd2{Delta} cells grown on YPL without ethanolamine is very low. As shown in Fig. 6, processing of pAPI in wild type, psd1{Delta}, psd2{Delta}, and cki1{Delta} dpl1{Delta} eki1{Delta} was identical, with no unprocessed precursor remaining. However, a dramatic difference in pAPI processing was observed with the unsupplemented and ethanolamine-supplemented psd1{Delta} psd2{Delta} double mutant. In the absence of ethanolamine, about 35% of precursor remained unprocessed, whereas the addition of ethanolamine led to maturation of pAPI comparable with wild type. Again, the same results were obtained with cells shifted to starvation medium for 4 h to induce autophagy (data not shown). Thus, the effect of severe PtdEtn depletion in psd1{Delta} psd2{Delta} is similar to that observed in vps4{Delta} or vps36{Delta}, which exhibit an enhanced requirement for this phospholipid.

The psd1{Delta} psd2{Delta} Mutant Shows Reduced Recruitment of Atg8p to the Preautophagosomal Structure and a Decrease in the Autophagy Rate—Atg8p is synthesized as a soluble precursor and conjugated to PtdEtn, which is essential for its proper localization and function in autophagy/the Cvt pathway (10, 12). In living cells, a functional GFP-Atg8p chimera has been localized to the PAS in addition to completely formed autophagosomes and Cvt vesicles (33). Localization of GFP-Atg8p to the PAS, which is believed to be a physiological intermediate structure for pAPI import into the vacuole and vesicle formation, is tightly coupled to Atg8p lipidation.

Interestingly, Atg8p levels of all mutants bearing defects in the different PtdEtn-synthesizing pathways were the same as in wild type (see Fig. 6), indicating that malfunction of autophagy in psd1{Delta} psd2{Delta} was not due to a limited amount of Atg8p. Therefore, we investigated whether the defect in maturation of pAPI upon PtdEtn depletion in the double mutant was reflected in defects in the organization of the PAS. For this purpose, we used a GFP-Atg8p hybrid and determined its presence in the PAS, indicated by the formation of a perivacuolar dot. Wild type and psd1{Delta} psd2{Delta} cells were grown on SL medium to the late logarithmic phase and shifted to starvation medium SL(–N) for 4 h. It has to be noted that the medium had to be supplemented with ethanolamine, since psd1{Delta} psd2{Delta} cells are strictly auxotrophic for ethanolamine on lactate synthetic minimal medium (1). Compared with wild type, psd1{Delta} psd2{Delta} cells exhibited a significantly reduced recruitment of GFP-Atg8p to the PAS (Fig. 7), which might be due to a decreased rate of autophagy in the mutant. To assess this hypothesis, we followed the selective vacuolar targeting of GFP-Atg8p as described before (32). As shown in Fig. 8, increasing levels of GFP accumulated in wild type cells during starvation. Compared with wild type, psd1{Delta} psd2{Delta} cells showed a significantly reduced rate of GFP formation, suggesting that autophagy proceeded at a reduced rate in this mutant. Thus, a certain level of PtdEtn appears to be necessary for the assembly of Atg8p to the PAS to form vesicles for vacuolar transport via autophagy.


   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
REFERENCES
 
In the yeast, PtdEtn was shown to affect various cellular processes, such as glycosylphosphatidylinositol anchor biosynthesis, targeting of amino acid transporters, cytokinesis, and autophagy (for a review, see Ref. 2). In this study, we present a screening for additional gene products with a specific requirement for PtdEtn, which identified VPS4 and VPS36. We show that a block in the CPY pathway caused by deletion of VPS4 or VPS36 affected an alternative route to the vacuole (i.e. autophagy/the Cvt pathway) (Fig. 1) and resulted in an increased requirement for PtdEtn for the assembly of Atg8p into membranes of the PAS. This view was supported by the fact that maturation of pAPI was defective in vps4{Delta} and vps36{Delta} mutants, although they exhibited wild type levels of PtdEtn and Atg8p. Supplementation with ethanolamine stimulated PtdEtn formation via the CDP-ethanolamine pathway and expression of Atg8p, providing the necessary amounts of both components for vesicle formation. Thus, PtdEtn is essential to overcome the autophagy defect in vps4{Delta} and vps36{Delta}.


Figure 7
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  		FIGURE 7.
Recruitment of GFP-Atg8p to the PAS. Wild type and psd1{Delta} psd2{Delta} cells expressing GFP-Atg8p were grown to the late logarithmic phase on SL medium supplemented with Etn and shifted to SL(–N) supplemented with Etn for 4 h. Cells were screened under the fluorescence microscope and cells with fluorescence signals on the PAS were counted.

 


Figure 8
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  		FIGURE 8.
Reduced rate of GFP-Atg8p degradation in the vacuole of psd1{Delta} psd2{Delta} cells. Cells expressing GFP-Atg8p from a centromeric plasmid under control of the ATG8 promoter were grown to the exponential growth phase in SL medium supplemented with Etn and starved for nitrogen in SL(–N) medium supplemented with Etn for the indicated times. Cell extracts were separated by SDS-PAGE and, after electroblotting on a nitrocellulose membrane, analyzed with an antibody against GFP.

 
The novel aspect of this work is that autophagy/the Cvt pathway and the CPY pathway are linked and balanced through the cellular PtdEtn level. We used the processing of the soluble vacuolar hydrolase API as a model to address this problem. API is synthesized as an inactive precursor and converted to its active form by the vacuolar proteinase A, Pep4p (34). Although some vps mutants are extremely defective in processing CPY and Pep4p, vps4{Delta} still exhibits substantial maturation of CPY, Pep4p, and proteinase B (35). Westphal et al. (36) claimed that an alternative mechanism of Pep4p sorting to the vacuole may exist, which involves a carrier protein (e.g. an integral membrane protein of the vacuole) that does not cycle between the late endosome and the Golgi complex but rather remains trapped in the late endosome or proceeds to the vacuole. The necessity of an alternative, CPY-independent delivery of Pep4p to the vacuole is most likely due to the central role of this enzyme as the primary activating protease for numerous vacuolar proenzymes. In the vps4{Delta} mutant, Pep4p seems to be present in its active form, although it is not known whether this protease is correctly localized to the vacuole or trapped within the class E organelle. One might assume, however, that a substantial amount of Pep4p reaches the vacuole, where it contributes to the breakdown of Cvt vesicles and autophagosomes. As a result, a large portion of pAPI can be correctly processed in vps4{Delta} and vps36{Delta}. Increased amounts of PtdEtn facilitating membrane assembly of Atg8p might be required to transport the amount of Pep4p to the vacuole via autophagy/the Cvt pathway, which is necessary to cleave the remaining portion of pAPI in vps4{Delta} and vps36{Delta}.

PtdEtn dependence of maturation of pAPI in vps4{Delta} and vps36{Delta} led us to speculate whether depletion of PtdEtn in general or depletion of the different PtdEtn pools provided by the three PtdEtn biosynthetic pathways had an effect on the transport of pAPI to the vacuole. Our results clearly demonstrate that severe depletion of PtdEtn in the psd1{Delta} psd2{Delta} mutant leads to an accumulation of pAPI (see Fig. 6). Thus, it appears to be PtdEtn depletion in general and not the effect of a specific PtdEtn biosynthetic route or pool that leads to defects in pAPI maturation. Because Atg8p expression was not compromised in the psd1{Delta} psd2{Delta} mutant, we concluded that the amount of PtdEtn was limiting. This was also reflected in a significant defect in recruitment of GFP-Atg8p to the PAS and a reduced autophagy rate in psd1{Delta} psd2{Delta}. Since stimulation of PtdEtn formation via the CDP-ethanolamine pathway rescued the autophagy defect, we assume that a minimum level of this phospholipid is essential for proper function of autophagy. Our experiments, however, do not exclude the possibility that PtdEtn depletion might also lead to a defect in membrane extension around the Cvt vesicles or autophagosomes, to a defect in the fusion of cytosolic vesicles with the vacuole, or to a defect in the breakdown of subvacuolar vesicles by Pep4p. A specific membrane composition may be required for the lysis of Cvt bodies and autophagic bodies. One component that has been shown to be involved in the degradation of vesicles is Cvt17p (37). Specific lipids could even provide the molecular basis for recognition within the vacuole lumen, allowing an alternate vacuolar lipase to distinguish between subvacuolar vesicles destined for degradation and the vacuolar membrane, which must remain intact.

A process related to Cvt/autophagy is pexophagy. Recent studies in our laboratory revealed that induction of yeast peroxisomes upon growth on oleate is delayed in strains with unbalanced PtdEtn biosynthesis.3 Upon the shift to glucose, peroxisomes are no longer required and rapidly degraded within the vacuole, either by micropexophagy or macropexophagy. Although these two processes are morphologically distinct, they seem to require the same set of proteins as starvation-induced macroautophagy (reviewed in Ref. 38). Interestingly, this process is not impaired in PtdEtn depleted strains.3 Thus, although PtdEtn is essential for vesicle formation during Cvt/autophagy, its depletion does not affect pexophagy in the same manner as Cvt/autophagy.

In summary, this study underlines the importance of PtdEtn for the cell as a mediator of complex processes. Thus, cellular PtdEtn homeostasis is essential not only to ensure structural integrity of membranes but also through its specific interaction with various components that govern organelle structure and function.


   FOOTNOTES
 
* This work was supported by the Fonds zur Förderung der Wissenschaftlichen Forschung in Österreich Project 17321 (to G. D.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Back

1 To whom correspondence should be addressed: Institute of Biochemistry, Graz University of Technology, Petersgasse 12/2, A-8010 Graz, Austria. Tel.: 43-316-873-6462; Fax: 43-316-873-6952; E-mail: guenther.daum{at}tugraz.at.

2 The abbreviations used are: PtdEtn, phosphatidylethanolamine; CPY, carboxypeptidase Y; Cvt, cytosol to vacuole targeting; pAPI, proaminopeptidase I; Etn, ethanolamine; PAS, preautophagosomal structure; PtdSer, phosphatidylserine; PVC, prevacuolar compartment; GFP, green fluorescent protein. Back

3 R. Nebauer, S. Rosenberger, and G. Daum, unpublished data. Back


   ACKNOWLEDGMENTS
 
We thank M. Thumm for kindly providing the pAPI and Atg8p antibodies and Y. Ohsumi for the GFP-Atg8p plasmid. We are indebted to A. Hermetter from our department for providing the Zeiss Axiovert 35 microscope (FWF Instrument).



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TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS
 DISCUSSION
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