Original Article

A Role for Actin, Cdc1p, and Myo2p in the Inheritance of Late Golgi Elements in Saccharomyces cerevisiae

Correspondence to: Benjamin S. Glick, Department of Molecular Genetics and Cell Biology, The University of Chicago, 920 East 58th St., Chicago, IL 60637. Tel:(773) 702-5315 Fax:(773) 702-3172 E-mail:bsglick{at}midway.uchicago.edu.

	Abstract

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

In Saccharomyces cerevisiae, Golgi elements are present in the bud very early in the cell cycle. We have analyzed this Golgi inheritance process using fluorescence microscopy and genetics. In rapidly growing cells, late Golgi elements show an actin-dependent concentration at sites of polarized growth. Late Golgi elements are apparently transported into the bud along actin cables and are also retained in the bud by a mechanism that may involve actin. A visual screen for mutants defective in the inheritance of late Golgi elements yielded multiple alleles of CDC1. Mutations in CDC1 severely depolarize the actin cytoskeleton, and these mutations prevent late Golgi elements from being retained in the bud. The efficient localization of late Golgi elements to the bud requires the type V myosin Myo2p, further suggesting that actin plays a role in Golgi inheritance. Surprisingly, early and late Golgi elements are inherited by different pathways, with early Golgi elements localizing to the bud in a Cdc1p- and Myo2p-independent manner. We propose that early Golgi elements arise from ER membranes that are present in the bud. These two pathways of Golgi inheritance in S. cerevisiae resemble Golgi inheritance pathways in vertebrate cells.

Key Words: Golgi apparatus, endoplasmic reticulum, budding yeast, actins, myosin

	Introduction

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

Eukaryotic cells partition each of their organelles during cell division. In budding yeasts such as Saccharomyces cerevisiae, organelles must be delivered to the emerging bud (Yaffe 1991 ). During S phase in S. cerevisiae, vacuoles and mitochondria are transported into the nascent bud by actin-dependent mechanisms (Hill et al. 1996 ; Simon et al. 1997 ; Catlett and Weisman 2000 ). The nuclear material then partitions between the mother and daughter cells in a process that requires microtubules (Hildebrandt and Hoyt 2000 ). Little is known about the inheritance of the ER and the Golgi apparatus, except that both of these organelles are present in the bud early in S phase (Segev et al. 1988 ; Redding et al. 1991 ; Preuss et al. 1991 , Preuss et al. 1992 ). We have initiated a molecular genetic analysis of Golgi inheritance in S. cerevisiae.

Ongoing studies of vertebrate cells have yielded two paradigms for Golgi inheritance. One paradigm states that the vertebrate Golgi fuses with the ER during mitosis and then reemerges to generate new Golgi stacks (Thyberg and Moskalewski 1998 ; Zaal et al. 1999 ). In S. cerevisiae, the analogous process would be the de novo formation of Golgi cisternae from ER membranes that are present in the bud. The other paradigm states that preexisting vertebrate Golgi fragments are partitioned between the two daughter cells during cytokinesis (Lowe et al. 1998 ). In S. cerevisiae, the analogous process would be the transfer of preexisting Golgi cisternae into the bud. These two postulated modes of Golgi inheritance are not mutually exclusive, either in vertebrate cells (Hammond and Glick 2000a ) or in budding yeasts.

The inheritance of the S. cerevisiae Golgi apparatus poses an interesting problem because this organelle does not assemble into stacks; instead, early and late cisternae are scattered throughout the cytoplasm (Segev et al. 1988 ; Franzusoff et al. 1991 ; Antebi and Fink 1992 ; Preuss et al. 1992 ; Lussier et al. 1995 ). We have proposed that this unusual Golgi organization is due to a delocalized transitional ER (tER)¹ compartment (Rossanese et al. 1999 ). The tER produces coat protein (COP) II transport vesicles, and accumulating evidence suggests that COPII vesicles ultimately give rise to new Golgi cisternae, implying that the Golgi can be viewed as an outgrowth of the tER (Bannykh and Balch 1997 ; Kuehn and Schekman 1997 ; Glick and Malhotra 1998 ; Pelham 1998 ). In S. cerevisiae, the entire ER apparently functions as tER (Rossanese et al. 1999 ), so new Golgi cisternae should form throughout the cytoplasm. Some of these new Golgi cisternae will form in the bud. Other Golgi cisternae that have been generated in the mother cell might subsequently be transferred into the bud. Our findings suggest that both of these mechanisms contribute to Golgi inheritance in S. cerevisiae.

	Materials and Methods

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

Strains, Media, and Growth Conditions
Yeast strains used in this study are shown in Table 1. Apart from Ypt1-A136D, all of these strains are derivatives of JK9-3d (Kunz et al. 1993 ). In the case of BGY104, the leu2-3,112 allele was converted to wild-type LEU2 by amplifying the wild-type LEU2 gene by PCR and using the resulting DNA fragment to transform the strain to leucine prototrophy. Green fluorescent protein (GFP) constructs were made using an enhanced GFP gene (EGFP; CLONTECH Laboratories, Inc.). Strains in which the SEC7 gene was replaced with SEC7–GFP were constructed as previously described (Seron et al. 1998 ). To obtain brighter fluorescence, additional strains were engineered, as described below, to express SEC7 fused to three tandem copies of GFP. pEGFP-1 (CLONTECH Laboratories, Inc.) was mutagenized to replace the GFP stop codon with GGTCCGG, creating a BspEI site. This intermediate plasmid, termed pEGFP-B1, was digested with BspEI and NotI, and an AgeI–NotI fragment from pEGFP-1 was inserted to yield pEGFP-12, which contains two tandem copies of GFP. The double GFP cassette was excised from pEGFP-12 with AgeI and NotI and subcloned into pEGFP-B1, as described above, to yield pEGFP-13, which contains three tandem copies of GFP. Finally, the triple GFP cassette was excised from pEGFP-13 with BamHI and NotI and subcloned into pUSE-URA3 (Seron et al. 1998 ), which had been digested with BamHI and EagI. The resulting plasmid was linearized with SpeI for pop-in–pop-out replacement of SEC7 with SEC7–GFPx3 (Rothstein 1991 ; Seron et al. 1998 ). Strains expressing SEC13-GFP were constructed as previously described (Rossanese et al. 1999 ).

Strains expressing SEC21-GFPx3 were constructed as described below. A DNA fragment comprising the last 205 nucleotides of the SEC21 gene plus 421 nucleotides downstream of the stop codon was amplified by PCR and was inserted into YIplac211 (Gietz and Sugino 1988 ), which had been cut with PvuII. The QuikChange method (Stratagene) was used to replace the stop codon of SEC21 with a BamHI–NotI cassette. Finally, the triple GFP cassette from pEGFP-13 was inserted as a BamHI–NotI fragment. The resulting construct was linearized with BclI for pop-in–pop-out replacement of SEC21 with SEC21-GFPx3. A similar strategy was used to replace RIC1 with RIC1–GFPx3, except that the final construct was linearized with PacI for integration. Strain BGY231, which expresses Mnt1p–Kre2p with a COOH-terminal triple myc tag (Jungmann and Munro 1998 ), was also generated by a pop-in–pop-out gene replacement.

Strains expressing GFP-YPT1 were constructed as described below. A BspHI site was introduced after the second codon of YPT1 (sequence from start codon: ATGAATGTCATGAGCGAG). Meanwhile, pEGFP-C1 (CLONTECH Laboratories, Inc.) was mutagenized to introduce an NcoI site between the BglII and EcoRI sites in the polylinker (sequence: AGATCTGCCATGGGAATTC). The GFP gene was excised from the resulting plasmid with NcoI and was inserted at the BspHI site in the modified YPT1 gene. Finally, a KpnI–BamHI fragment containing GFP-YPT1 under control of the YPT1 promoter was inserted into the corresponding sites in YIplac128 (Gietz and Sugino 1988 ). The resulting plasmid was linearized with ClaI and integrated into the LEU2 locus.

Strains containing GFP–HDEL in the ER lumen were constructed as described below. An EcoRV–HindIII fragment containing the CYC1 transcription terminator (Osborne and Guarente 1989 ) was inserted into YIplac204 (Gietz and Sugino 1988 ), which had been cut with HincII and HindIII. The resulting plasmid was digested with EheI and SmaI, and a fusion (generated by overlap extension PCR; Ho et al. 1989 ) of the TPI1 promoter to the first 135 nucleotides of the KAR2 gene was inserted. Finally, the GFP gene was amplified by PCR and simultaneously modified to encode a COOH-terminal HDEL tetrapeptide, and this PCR fragment was inserted into the previous construct as a BamHI–XbaI fragment. The final construct encodes the Kar2p presequence joined to the NH₂ terminus of GFP–HDEL by the linker peptide ADDGDPPVAT. This plasmid was linearized with EcoRV and integrated into the TRP1 locus.

Expression of ER-targeted GFP–HDEL did not significantly affect cell growth. The GFP–YPT1 fusion gene is functional, as judged by its ability to rescue growth of the thermosensitive Ypt1–A136D strain at 37°C; however, GFP–Ypt1p sometimes had a clumpy appearance in slowly growing cells, suggesting that this fusion protein is subtly different from authentic Ypt1p. The GFP fusions with SEC7, SEC13, and SEC21 are also functional, as judged by their ability to support normal growth in place of the cognate chromosomal genes. Previous work has established that GFP-tagged Ric1p is functional (Siniossoglou et al. 2000 ). In the case of Sec7p, Sec21p, and Ric1p, the single GFP–tagged versions seem to behave identically to the triple GFP–tagged versions with respect to protein localization and cell growth, indicating that these proteins tolerate the triple GFP tag.

The act1-DSE and myo2-66 mutations were introduced into JK9-3da by the pop-in–pop-out method (Rothstein 1991 ). After the integrated plasmids had been popped out, the presence of the mutant alleles was confirmed by PCR amplification and sequencing of the relevant genomic DNA regions. To generate the act1-DSE replacement construct, the act1-DSE allele was excised from pCEN-DSE (Cook et al. 1992 ) with AflIII, blunted with Klenow, and inserted into the Ecl136II site of pUC19-URA3 (Rossanese et al. 1999 ). The resulting plasmid was linearized with SspI for integration. To generate the myo2-66 replacement construct, a DNA fragment containing a 3' portion of the myo2-66 allele (Johnston et al. 1991 ) was excised by digesting with ClaI, blunting with Klenow, and digesting with SalI; this fragment was then subcloned into pUC19-URA3, which had been digested with Ecl136II and SalI. The resulting plasmid was linearized with BamHI for integration.

Unless otherwise indicated, yeast strains to be viewed by fluorescence microscopy were grown in a minimally fluorescent quasi-synthetic dextrose medium (QSD) (0.67% yeast nitrogen base, 2% glucose, 0.01% CaCl₂•2H₂O, 0.05% NaCl, 0.05% MgCl₂•6H₂O, 0.1%NH₄Cl, 0.5% KH₂PO₄, 0.1% K₂HPO₄, 1X complete supplemental mixture [Bio101]). QSD yields very rapid growth and has a relatively low background fluorescence. Some experiments used rich medium (YPD) (1% yeast extract, 2% peptone, 2% glucose, 20 mg/liter adenine sulfate, 20 mg/liter uracil).

Antibodies
The following antibodies and concentrations were used for immunofluorescence. Mouse monoclonal anti–ß-tubulin (clone KMX-1; Roche) was used at 1 µg/ml, and anti-GFP (a mixture from clones 7.1 and 13.1; Roche) was used at 5 µg/ml. Rabbit polyclonal anti-GFP (CLONTECH Laboratories, Inc.) was used at 1:200 dilution. Rabbit polyclonal anti-Sec7p (Franzusoff et al. 1991 ), affinity purified as described (Harlow and Lane 1988 ) against a fusion protein comprising glutathione S-transferase linked to the NH₂-terminal acidic portion of Sec7p (Rossanese et al. 1999 ), was used at 1:100 dilution. Fluorescent secondary antibodies from donkey (Jackson ImmunoResearch Laboratories) were used at 1:200 dilution.

Viewing Intracellular Structures by Fluorescence Microscopy
Immunofluorescence microscopy of yeast was performed as previously described (Rossanese et al. 1999 ). Cells expressing a GFP fusion or cells that had been stained with FM4-64 (N-(3-triethylammoniumpropyl)-4-(6-(4-(diethylamino)phenyl)hexatrienyl) pyridinium dibromide; Molecular Probes) were incubated under the appropriate conditions and then fixed as described below. A 0.4-ml aliquot of a yeast culture was mixed with an equal volume of ice-cold 2X fixative (100 mM potassium phosphate, pH 6.5, 2 mM MgCl₂, 8% formaldehyde, 0.5% glutaraldehyde). After 1 h on ice in the dark, the cells were washed twice with 1 ml PBS and resuspended in 50 µl PBS. For viewing, 1.5 µl of the resuspended cells was placed on a glass slide and spread with a coverslip.

Vacuoles were labeled by the method of Hill et al. 1996 . Cells were grown in QSD to an OD₆₀₀ of 0.8–1.0, and a 0.25-ml aliquot of the culture was incubated for 1 h at room temperature in the dark with 80 µM FM4-64, diluted from a 3.3 mM stock solution in DMSO. The cells were washed three times with 1 ml QSD, diluted into 2–5 ml QSD, and allowed grow for an additional 2–4 h. Finally, the cells were resuspended in 0.1 ml QSD and fixed as above.

Actin was visualized as described below. A yeast culture was grown overnight with good aeration to an OD₆₀₀ of 1, and fixed as above. After the final wash, the cells were resuspended in PBS, pH 7.4, 0.5% octyl glucoside, to an OD₆₀₀ of 10. Then, 92.4 µl of cell suspension was transferred to a microfuge tube, and 7.6 µl of Alexa 594–phalloidin (6.6 µM in methanol; Molecular Probes) was added while vortexing, yielding a final Alexa 594–phalloidin concentration of 0.5 µM. The sample was mixed end-over-end for 1 h in the dark. Cells were washed three times with 200 µl cold PBS. After the final wash, the cells were resuspended in 10 µl phenylenediamine-containing mounting medium (Pringle et al. 1991 ). 1.5 µl of this suspension was mounted and viewed.

Fluorescence and differential interference contrast (DIC) imaging, photography, and image processing were carried out as previously described (Rossanese et al. 1999 ).

Treatment with -Factor, Latrunculin A, and Nocodazole
Cells to be treated with -factor were grown overnight in YPD at 30°C (or 23°C for thermosensitive mutants) to an OD₆₀₀ of 0.8–1.0, centrifuged, and resuspended to the same OD₆₀₀ in fresh YPD. -Factor was added to a final concentration of 0.5 µM from a 1 mg/ml (594 µM) stock in DMSO, and the culture was incubated with shaking for 90 min. For treatment with latrunculin A (LatA) or nocodazole, cells were grown overnight in QSD to an OD₆₀₀ of 1. Then a 400-µl aliquot was transferred to a microfuge tube, and 4 µl of either 20 mM LatA or 1.5 mg/ml nocodazole in DMSO (Molecular Probes) was added while vortexing to give a final concentration of 200 µM LatA or 15 µg/ml nocodazole. Control aliquots received an equal volume of DMSO. The cells were transferred to a 5-ml Falcon tube, returned to 30°C with shaking for 30 min, and then fixed and either stained with Alexa 594–phalloidin to visualize actin (see above) or processed for immunofluorescence using an antitubulin antibody (Rossanese et al. 1999 ). As previously reported, LatA caused a rapid depolymerization of actin cables and patches (Ayscough et al. 1997 ), whereas nocodazole caused a rapid depolymerization of microtubules (Jacobs et al. 1988 ).

Isolation of the Mutant Strains
Strain BGY103 was mutagenized to 3–5% survival by treatment with ethyl methanesulfonate (Lawrence 1991 ). The following method was used for rapid identification of temperature-sensitive mutants. Mutagenized cells were plated on 150-mm-diam YPD plates and grown at 23°C to yield 5,000 colonies per plate. Each plate was replica-plated onto a fresh YPD plate for growth at 37°C, and onto a second YPD plate for growth at 23°C. After a suitable growth period, the 37°C and 23°C plates were photocopied to yield images of white colonies on a black background. (This step was facilitated by using relatively thin YPD plates.) The image of the 37°C plate was scanned with a Hewlett-Packard ScanJet 4c scanner, using the DeskScan II software set to "sharp black and white drawing". This image was imported into Adobe^® Photoshop^TM and inverted, yielding an image of black colonies on a clear background. This inverted image was printed onto a transparency and overlaid on the photocopy of the 23°C plate. The black spots on the transparency obscured the underlying white spots, except in the case of clones that had failed to grow at 37°C. Colonies that appeared as white in this assay were subjected to a second round of testing, and 70% turned out to be bona fide temperature-sensitive mutants. Using this procedure, we isolated 4,000 temperature-sensitive derivatives of BGY103.

These mutants were screened as described below for alterations in Golgi inheritance or morphology. Mutant clones were grown in QSD in 96-well plates, with shaking for 2 d at room temperature. The cultures were then diluted 1:1 into fresh QSD, grown at room temperature for an additional 4–6 h, and shifted to 37°C for 2 h before viewing. A ceramic benchtop 96-well plate warmer (Thermolyne) was used to maintain the samples at 37°C during the viewing process, and a second plate warmer was used to prewarm the microscope slides. From each well in the plate, 1.5 µl was pipetted onto a prewarmed slide and spread with a 22-mm glass coverslip. Cells were viewed by fluorescence and DIC microscopy to evaluate Golgi inheritance and morphology. Using this visual screen, we typically examined two 96-well plates per day. Mutants with interesting Golgi patterns were subjected to additional rounds of screening, and those that displayed reproducible phenotypes were chosen for further analysis.

Quantitation of Organellar Inheritance
To quantify the rates of organellar inheritance, randomly chosen fields of cells were photographed in both DIC and fluorescence modes. A single DIC image was captured while fluorescence images were collected as a stack and then deconvolved and projected (Rossanese et al. 1999 ). Analyses were performed with Adobe^® Photoshop^TM and NIH Image (National Institutes of Health). Using the DIC images, all of the visibly budded cells were chosen, and each cell was assigned to one of five bud size categories based on the cross-sectional area of the bud, as measured with NIH Image. Category I buds had cross-sectional areas between 4.0 and 7.4% of the average cross-sectional area of the mother cells. The corresponding percentages for the other bud size categories were as follows: category II, 7.5–10.9%; category III, 11.0–14.4%; category IV, 14.5–17.9%; category V, 18.0–21.4%. Assuming that the cells were spherical, the bud volumes as a percentage of the average mother cell volume can be estimated as follows: category I, 0.8–2.0%; category II, 2.1–3.6%; category III, 3.7–5.5%; category IV, 5.5–7.6%; category V, 7.6–9.9%. The examination of budded cells was continued until 20 cells had been identified for each bud size category. The corresponding fluorescence images were then examined with Photoshop^TM, and each bud was scored for the presence or absence of fluorescent structures. For each of the plots in the figures, two separate experiments were performed, and the numbers were combined. Unless otherwise indicated, the different curves in a given plot compare cultures that were incubated under identical growth conditions.

Cloning of CDC1
The gene that is defective in the class A mutants was cloned by backcrossing one of these mutant strains four times to the parental strain (using BGY104 for the first backcross) to yield strain BGY105, and then transforming BGY105 with a URA3 CEN yeast genomic DNA library (a gift of Mark Hochstrasser (Yale University, New Haven, CT); Rose et al. 1987 ) and selecting for restoration of growth at 37°C. Fluorescence microscopy confirmed that the complementing plasmids also restored normal Sec7p–GFP inheritance. Sequencing and subcloning showed that the complementing gene was CDC1. Therefore, the backcrossed mutant strain was designated cdc1-304. We used two approaches to confirm that CDC1 is the relevant gene. First, genomic DNA samples from the parental and cdc1-304 strains were used for PCR amplification of the corresponding CDC1 alleles, which were cloned into plasmid YCplac33 (Gietz and Sugino 1988 ). The wild-type CDC1 allele complemented the high temperature growth defect of the mutant strain, whereas the cdc1-304 allele showed no complementation. Second, CDC1 is only 25 kb from SEC7 on chromosome IV, implying that the mutations in the class A strains should be tightly linked to the SEC7–GFP marker. To test this prediction, a cdc1-304 SEC7–GFP strain was mated with a CDC1 SEC7 strain, and the resulting diploid was sporulated. As expected, most of the tetrads failed to segregate the temperature-sensitive growth phenotype away from the fluorescence conferred by SEC7–GFP.

Confocal Microscopy of Living Cells
Cells of strain BGY316 or BGY111 were grown in QSD at room temperature to an OD₆₀₀ of 0.5. To immobilize the cells for imaging, a T dish (Bioptechs) was pretreated with a 2 mg/ml solution of concanavalin A (Sigma-Aldrich), allowed to dry, and washed with distilled water. An aliquot of the culture was added to the dish and left undisturbed for 30 min. Unbound cells were then removed by gentle washing. For imaging, the immobilized cells were gradually shifted to 37°C over a period of 20 min and were held at 37°C for an additional 1.5–2 h. Temperature control was achieved using Bioptechs T and objective controllers. Single cells were imaged repeatedly with a 100X 1.4-NA PlanApo objective and a ZEISS Axiovert microscope, equipped with an LSM 510 confocal scanner. A piezoelectric objective controller was used to drive continuous objective movement, thereby allowing for the rapid collection of four-dimensional data sets (Hammond and Glick 2000b ). The GFP signal was visualized by excitation with a 488-nm laser and collection with a 505-nm longpass filter. Complete z-stacks were captured at intervals of 2.5 s, with the pinhole adjusted to yield 1.2 Airy units and a z-axis spacing of 0.35 µm between optical sections. Transmitted light images of the cells were collected simultaneously. The fluorescence images were processed with a 3 x 3 hybrid median filter to remove shot noise and then were projected using an average intensity algorithm that included multiplying the pixel values by an appropriate scaling factor to provide adequate contrast (Hammond and Glick 2000b ). Transmitted light images were projected using a maximum intensity algorithm. These filtering and projection operations were performed using custom macros written in NIH Image. The projected fluorescence and transmitted light images were merged using Adobe^® Photoshop^TM.

	Results

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

Analyzing Golgi Inheritance in S. cerevisiae
To visualize the Golgi in S. cerevisiae, we have fused GFP to proteins that are associated with the cytosolic face of Golgi membranes. This strategy was chosen because GFP folds more efficiently in the cytosol than in the lumen of the yeast secretory pathway (Wooding and Pelham 1998 ). GFP can be linked to the cytosolic portions of integral Golgi membrane proteins (Wooding and Pelham 1998 ), but such constructs often yield a background ER fluorescence under suboptimal growth conditions (not shown). Therefore, we used peripherally associated Golgi membrane proteins. For most of our experiments, the SEC7 gene was replaced with a SEC7–GFP fusion gene (Seron et al. 1998 ). Sec7p is an abundant peripheral membrane protein of the late Golgi complex (Franzusoff et al. 1991 ), and, in a typical cell, Sec7p–GFP labels 10–15 cytoplasmic spots that apparently correspond to individual Golgi cisternae (Preuss et al. 1992 ; Seron et al. 1998 ).

The first question that arose was: how should we define Golgi inheritance? In studies of mitochondria and vacuoles, inheritance has been defined as the transfer of preexisting organellar material from the mother cell into the bud (Yaffe 1991 ; Catlett and Weisman 2000 ). However, mitochondria and vacuoles are long-lived entities, whereas yeast Golgi cisternae are probably transitory structures with a lifetime of only a few minutes (Wooding and Pelham 1998 ; Morin-Ganet et al. 2000 ). As described in the Introduction, Golgi cisternae might localize to the bud either by the transfer of preexisting cisternae or by de novo formation. These practical and theoretical considerations led us to define Golgi inheritance as the presence of Golgi elements in the bud. The amount of Golgi material in the bud varies widely under different growth conditions, but almost every bud contains some Golgi elements under all growth conditions (see below). Thus, for quantitative studies, we chose to assay simply for the presence or absence of a fluorescent Golgi marker in the bud.

Actin-dependent Concentration of Sec7p–GFP at Sites of Polarized Growth
Sec7p–GFP has previously been visualized as a set of spots distributed essentially evenly throughout the mother and daughter cells (Seron et al. 1998 ). However, Preuss et al. 1992 reported in an electron microscopy study that Golgi cisternae are clustered at the incipient bud site, within the bud, and at sites of cell wall synthesis during cytokinesis. This variability in the distribution of Golgi elements apparently reflects the growth state of the cells. Under many growth conditions, Sec7p–GFP shows little or no polarization; but in cultures that are growing very rapidly, Sec7p–GFP is clearly polarized (Fig 1 A, bottom).

View larger version (69K): [in this window] [in a new window]   Figure 1. Sec7p–GFP is concentrated at sites of polarized growth in rapidly growing or schmooing cells. (A) Visualization of actin and Sec7p–GFP through the cell cycle. An unsynchronized culture of BGY316 cells growing rapidly at 30°C was fixed and stained with Alexa 594–phalloidin. The cells were then imaged by DIC microscopy and dual-color fluorescence microscopy. Numbers mark examples of a nonpolarized G1 cell (1), a polarized G1 cell (2), an S phase cell (3), and a cell undergoing cytokinesis (4). Actin patches and Sec7p–GFP are both concentrated at sites of polarized growth. (B) Distributions of actin and Sec7p–GFP in schmooing cells. A BGY316 culture was treated with -factor for 90 min at 30°C, and then fixed and viewed as in A. Actin patches and Sec7p–GFP are concentrated in the schmoo. (C) Effects of disrupting actin or microtubules on the Sec7p–GFP pattern in rapidly growing cells. Aliquots of a rapidly growing BGY316 culture were either left untreated (DMSO), or treated with 200 µM LatA or 15 µg/ml nocodazole (Noc) for 30 min at 30°C before fixation. A portion of each aliquot was stained with Alexa 594–phalloidin to confirm that actin polymers had been disrupted by LatA, and a second portion was processed for immunofluorescence to confirm that microtubules had been disrupted by nocodazole (not shown). 50 budded cells from each aliquot were examined as in A, and the results from two separate experiments were combined. A cell was scored as having polarized Sec7p–GFP if it displayed a clear concentration of fluorescence in or near the bud. As judged by this assay, the polarization of Sec7p–GFP is effectively abolished by LatA treatment but is unaffected by nocodazole treatment. Bars, 2 µm.

The Sec7p–GFP pattern in rapidly growing cells is reminiscent of the distribution of actin patches, which mark sites of polarized growth (Ayscough and Drubin 1996 ; Botstein et al. 1997 ). Therefore, we used fluorescence microscopy to compare the locations of actin and Sec7p–GFP (Fig 1 A, middle and bottom). The numbers 1–4 indicate cells at different stages of the cell cycle (Lew et al. 1997 ). In early G1 cells (1), neither actin nor Sec7p–GFP shows detectable polarization. In late G1 cells (2), actin patches and Sec7p–GFP are both concentrated at the incipient bud site. As actin patches move into the bud during S phase (3), Sec7p–GFP becomes concentrated in the bud. When actin patches repolarize to the sites of cytokinesis (4), Sec7p–GFP is also concentrated at these sites. Although the fluorescence patterns of actin patches and Sec7p–GFP do not actually overlap, these two patterns are similar throughout the cell cycle, confirming that late Golgi elements preferentially localize to sites of polarized growth.

An alternative way to induce Sec7p–GFP polarization is to expose haploid MATa cells to the pheromone -factor (Sprague and Thorner 1992 ). This treatment arrests the cell cycle in G1 and induces the formation of a mating projection, or schmoo. In -factor–treated cells, Sec7p–GFP is almost always concentrated near the schmoo tip (Fig 1 B). This result fits with an electron microscopy study that reported a clustering of Golgi cisternae in the schmoo (Baba et al. 1989 ). Thus, Sec7p–GFP is concentrated at sites of polarized growth in rapidly growing or schmooing cells.

One possible interpretation of these data is that late Golgi elements are transported along actin cables to sites of polarized growth. If so, then disrupting the actin cytoskeleton should abolish the polarization of Sec7p–GFP. To test this prediction, we treated a rapidly growing culture with LatA to block actin polymerization (Ayscough et al. 1997 ). LatA treatment disrupts dynamic actin structures, including cables and patches. In a mock-treated culture, 80% of the budded cells showed clustering of Sec7p–GFP in or near the bud, whereas in the LatA-treated culture, <5% of the budded cells showed clustering of Sec7p–GFP (Fig 1 C). As a control, when the culture was treated with nocodazole to depolymerize microtubules (Jacobs et al. 1988 ), Sec7p–GFP remained polarized (Fig 1 C). This result matches our prediction. However, it should be noted that the LatA approach has two caveats. First, LatA-treated cells often abandon their current bud and choose a different bud site (Ayscough et al. 1997 ). Therefore, the loss of Sec7p–GFP polarization might reflect a general loss of cellular polarity cues. Second, cells that are growing suboptimally exhibit reduced polarization of Sec7p–GFP (see above), so LatA treatment might indirectly depolarize Sec7p–GFP by inhibiting cell growth. Despite these qualifications, our results support the idea that late Golgi elements undergo actin-dependent transport to sites of polarized growth.

LatA-resistant Localization of Sec7p–GFP to the Bud
Our goal is to understand how Golgi structures are incorporated into the newly formed bud. Initially, the most appealing idea was that late Golgi elements localize to the bud solely because of actin-dependent transport to sites of polarized growth. As predicted by this model, cells treated with LatA exhibit reduced Sec7p–GFP fluorescence in the bud (Fig 2 A). A further prediction is that the Golgi elements in LatA-treated cells should be distributed randomly in the cytoplasm so that many of the small buds (i.e., those with volumes <10% of the average mother cell volume) should be devoid of Sec7p–GFP. For example, if the bud volume is 2% of the mother cell volume, and if the cell contains 15 randomly distributed fluorescent Golgi elements, then the probability that the bud contains one or more fluorescent Golgi elements is only 25%. Surprisingly, however, most of the budded cells in a LatA-treated culture contain at least one spot of Sec7p–GFP fluorescence in the bud (Fig 2 A). To quantify this effect, budded cells were scored using a plus–minus assay for the presence of Sec7p–GFP fluorescence in the bud. Under normal growth conditions (Fig 2 B, ), Sec7p–GFP is inherited very early, with 70–90% of the nascent buds containing Sec7p–GFP by the time the bud volume reaches 0.8–2.0% of the average mother cell volume (category I). When the bud volume reaches 3.7–5.5% of the average mother cell volume (category III), essentially all of the buds contain Sec7p–GFP. Treatment with LatA (Fig 2 B, •) reduces the percentage of category I buds that contain Sec7p–GFP, but otherwise the numbers for control and LatA-treated cells are indistinguishable. For all of the bud size categories, the percentage of the buds that contain Sec7p–GFP after LatA treatment is much higher than predicted for a random distribution. This result indicates that a LatA-resistant mechanism localizes a subset of the late Golgi elements to the bud.

View larger version (55K): [in this window] [in a new window]   Figure 2. A subset of the late Golgi elements localize to the bud even after LatA treatment. (A and B) As described in the legend to Fig 1 C, a rapidly growing BGY316 culture was treated with LatA for 30 min before fixation. Merged DIC and fluorescence images of representative LatA-treated cells are shown in A. Sec7p–GFP is generally depolarized, yet most of the small buds contain at least one spot of Sec7p–GFP fluorescence. This residual Sec7p–GFP inheritance is quantified in B. As described in Materials and Methods, budded cells from cultures mock treated with DMSO () or treated with LatA (•) were assigned to five categories on the basis of bud size, with category I cells having the smallest buds and category V the largest. Each budded cell was scored in a plus–minus manner for the presence of Sec7p–GFP in the bud. The results indicate that LatA treatment causes only a minor reduction in the percentage of buds containing Sec7p–GFP. (C and D) Cultures carrying the wild-type ACT1 gene (strain BGY316; ) or the act1-DSE allele (strain BGY414; •) were grown at 30°C, labeled with FM4-64, and fixed. Using the plus–minus visual assay, budded cells were assessed for the inheritance of vacuoles (C) and Sec7p–GFP (D). The act1-DSE mutation inhibits vacuolar inheritance but has no effect on Sec7p–GFP inheritance. Bar, 2 µm.

One limitation of these LatA experiments is that severe disruption of the actin cytoskeleton blocks bud formation, restricting the analysis to buds that were present before addition of the drug (Ayscough et al. 1997 ; Botstein et al. 1997 ). A gentler approach is to compromise actin function while still allowing the cells to grow in a polarized manner. For example, DSE actin lacks the three residues that follow the initiator methionine (Cook et al. 1992 ), and act1-DSE cells grow at essentially wild-type rates but have defects in myosin-driven transport (Cook et al. 1992 ; Hill et al. 1996 ). Rather than using an existing act1-DSE strain, we introduced the act1-DDSE allele into our standard genetic background (Table 1) because we find that different laboratory strains inherit various organelles at different stages of bud development. It was previously reported that act1-DSE cells are strongly defective in vacuolar inheritance (Hill et al. 1996 ). We could readily verify this result. In our wild-type strain (Fig 2 C, ), vacuoles are inherited later than are the Golgi elements, but nearly all of the buds contain maternally derived vacuolar material by the time the buds reach 7.6–9.9% of the mother cell volume (category V). In cells carrying the act1-DSE allele (Fig 2 C, •), vacuolar inheritance is dramatically inhibited. By contrast, ACT1 and act1-DSE cells are similar with regard to the percentage of buds that contain Sec7p–GFP (Fig 2 D). To extend this analysis, we introduced SEC7–GFP into a set of yeast strains in which various charged-to-alanine codon substitutions had been made in the ACT1 gene (Wertman et al. 1992 ). Many of these act1 strains exhibit defects in the morphology and inheritance of vacuoles and mitochondria (Drubin et al. 1993 ; Smith et al. 1995 ; Hill et al. 1996 ); but as judged by our plus–minus visual assay, each of the act1 mutants efficiently localizes Sec7p–GFP to the bud (not shown). Thus, a variety of conditions that are routinely used to disrupt the actin cytoskeleton do not block Sec7p–GFP inheritance.

These findings demonstrate that an intact actin cytoskeleton is not essential for inheriting the late Golgi complex. One possible interpretation is that an actin-independent process localizes a subset of the late Golgi elements to the bud. However, it is also possible that LatA-treated cells and act1 mutant cells still contain residual actin structures in the bud, and that this residual bud-localized actin is required for efficient Golgi inheritance. As described below, our combined data favor this second possibility.

Isolation of Mutants with Altered Golgi Inheritance
To gain molecular insights into Golgi inheritance, we decided to take a genetic approach. The first step was to generate mutant derivatives of a strain expressing Sec7p–GFP. Because Golgi inheritance is presumably essential for viability, our analysis focused on mutants that were temperature sensitive for growth. 4,000 temperature-sensitive mutants were collected using a rapid screening procedure (Materials and Methods). Each of these mutants was grown at the permissive temperature, shifted briefly to 37°C, and viewed by DIC and fluorescence microscopy to ascertain whether Sec7p–GFP was present in the small buds.

We identified 14 mutants that have normal patterns of Sec7p–GFP fluorescence in the mother cell but frequently lack Sec7p–GFP in the small buds. These Golgi inheritance mutants were designated class A (Fig 3 A). The class A mutants all carry recessive single gene mutations, and they fall into a single complementation group. Therefore, we focused on a class A mutant that consistently showed a strong phenotype and backcrossed this mutant to the parental strain to transfer the mutation into a clean genetic background. Fig 3 B shows a quantitation of the Golgi inheritance defect in this representative class A mutant. In wild-type cells, Sec7p–GFP is present in 70% of the category I buds and in essentially all of the category III buds. In the class A mutant, Sec7p–GFP is present in only 15% of the category I buds and 70% of the category III buds. Only when the class A buds reach 7.6–9.9% of the average mother cell volume (category V) do virtually all of the buds contain Sec7p–GFP. Therefore, the class A mutants define a genetic locus that is essential for normal Golgi inheritance.

View larger version (59K): [in this window] [in a new window]   Figure 3. Mutants with altered inheritance or morphology of Sec7p–GFP-labeled Golgi elements. Cultures were grown overnight at room temperature and then shifted to 37°C for 1 h before fixation. (A) Golgi distribution and morphology in the four classes of mutants. DIC and fluorescence images were captured separately and merged. In class A mutants, the Sec7p–GFP-labeled Golgi elements exhibit normal size and distribution within the mother cell, but are frequently absent from the small buds. Strain BGY105 is shown. Class B mutants contain larger, fewer Golgi elements than wild-type cells. A typical class B cell has one to three large spots of Sec7p–GFP fluorescence. In class C mutants, the Golgi elements are smaller and more numerous than in wild-type cells. Moreover, class C mutants often display an even stronger polarization of late Golgi elements than do wild-type cells. The single class D mutant has a variety of Golgi morphology defects: Sec7p–GFP fluorescence can appear as rings, bars, or thin lines. (B) Cultures of wild-type cells (strain BGY316; ) and a representative class A mutant (strain BGY111; •) were grown at room temperature and then shifted to 37°C for 1 h before fixation. Quantitation by the plus–minus visual assay confirmed that Sec7p–GFP inheritance is defective in the class A mutant. Bar, 2 µm.

During the course of this screen for Golgi inheritance mutants, we also identified three classes of mutants with abnormal patterns of Sec7p–GFP fluorescence (Fig 3 A). Class B mutants contain only one or a few large Sec7p–GFP-labeled Golgi elements per cell. The buds of class B mutants often lack Sec7p–GFP, but this inheritance defect is probably a secondary consequence of the altered Golgi structure. All six of the class B strains carry single gene recessive mutations, and these mutants fall into a single complementation group. In class C mutants, the Sec7p–GFP-labeled Golgi elements are smaller and more numerous than in the wild type. Moreover, class C mutants display an exaggerated form of the Sec7p–GFP polarization that is sometimes observed in wild-type cells (Fig 1 A). We isolated 15 class C mutants, which fall into multiple complementation groups; genetic characterization of these strains is in progress. In the single class D mutant, the Sec7p–GFP-labeled Golgi elements display a variety of unusual shapes. Tetrad analysis revealed that the abnormal Golgi phenotype of class D cells is the result of a single recessive mutation that does not cosegregate with the temperature sensitivity phenotype. Although the class B, C, and D mutants are not specifically defective in Golgi inheritance, they will likely be useful for understanding the mechanisms that control Golgi distribution.

The Class A Phenotype Results from Mutations in CDC1
To identify the genetic locus that is mutated in class A cells, we isolated plasmids that rescue both growth and Sec7p–GFP inheritance at 37°C. Sequencing and subcloning revealed that the complementing DNA fragment is the CDC1 gene (Halbrook and Hoekstra 1994 ), and additional experiments confirmed that the defective Sec7p–GFP inheritance of class A mutants is due to alterations in CDC1 (Materials and Methods). The cdc1 allele in the representative class A mutant of Fig 3 was designated cdc1-304. This allele contains a single base change that converts the codon for histidine-323 (CAC) to an asparagine codon (AAC).

cdc1 mutants were originally isolated as temperature-sensitive strains that arrested with small buds, 2N DNA, and undivided nuclei (Hartwell et al. 1970 ). However, subsequent work indicated that cdc1 cells can arrest either without a bud or with a small bud, pointing to a role for Cdc1p at multiple stages of the cell cycle (Hartwell 1971 ; Paidhungat and Garrett 1998b ). This heterogeneous arrest phenotype discounts CDC1 as a true cell division cycle gene. Recent studies suggest a link between Cdc1p and divalent cation metabolism (see Discussion), but the function and localization of Cdc1p are unknown. Therefore, we undertook further experiments to clarify the role of Cdc1p in Golgi inheritance.

The cdc1-304 Mutant Shows Defects in Actin Organization and Golgi Retention
The first question was whether the polarity defects in cdc1 cells are restricted to Golgi inheritance. We examined actin distribution in wild-type and cdc1-304 cultures that had been incubated at 37°C for 1 h (Fig 4 A). In wild-type cells, actin patches are concentrated at sites of polarized growth, and cables are visible in the mother cells. By contrast, actin polarity is largely abolished in cdc1-304 cells; patches are distributed evenly throughout the mother and bud, and cables are rarely visible. Because a polarized actin cytoskeleton is needed for vacuolar inheritance (Catlett and Weisman 2000 ), this process should also be disrupted by the cdc1-304 mutation. Indeed, vacuolar inheritance at 37°C is slower in the cdc1-304 strain than in the corresponding wild-type strain (Fig 4 B). Vacuolar morphology is also abnormal in the cdc1-304 strain, with many of the cells containing clusters of vacuolar fragments (not shown). These data indicate that Cdc1p influences the distribution of multiple cellular components.

View larger version (59K): [in this window] [in a new window]   Figure 4. The cdc1-304 mutant exhibits defects in actin polarity and vacuolar inheritance. (A) Wild-type (BGY316) and cdc1-304 (BGY111) cultures were grown at room temperature, shifted to 37°C for 1 h, fixed, and stained with Alexa 594–phalloidin. Fluorescence images are shown. Most of the wild-type cells contain polarized actin patches and cables, whereas most of the cdc1-304 cells contain depolarized patches and few visible cables. (B) Wild-type and cdc1-304 cultures were grown at room temperature, labeled with FM4-64, and then shifted to 37°C for 1 h. The presence of maternally derived vacuolar material in the bud was quantified as described in the legend to Fig 2 C. The cdc1-304 mutant shows a delay in vacuolar inheritance. Bar, 2 µm.

Can the defective inheritance of Sec7p–GFP in cdc1-304 cells be explained by the loss of actin polarity? We found previously that when the actin cytoskeleton is extensively disrupted with LatA, Sec7p–GFP is still inherited efficiently (Fig 2). However, because LatA selectively inhibits actin polymerization (Ayscough et al. 1997 ), any polymerized actin structures will not be affected by this drug. We speculate that the bud contains residual actin structures that are resistant to disruption by LatA (Karpova et al. 2000 ) and that a subset of the late Golgi elements are retained in the bud by association with this residual bud-localized actin. Presumably, the cdc1-304 mutation inhibits late Golgi inheritance by disrupting not only the actin cables but also the bud-localized actin. This model predicts that in a cdc1-304 cell, Sec7p–GFP should localize to the bud but will fail to be retained there. To test this prediction, we repeatedly imaged Sec7p–GFP in individual CDC1 and cdc1-304 cells at 37°C (Fig 5). Complete confocal z-stacks were captured at intervals of 2.5 s. Because the Golgi of S. cerevisiae is highly dynamic (Wooding and Pelham 1998 ), the overall pattern of Sec7p–GFP fluorescence changes significantly between each time point, even with this rapid imaging protocol; but we were able to assess the gain or loss of fluorescence in small buds. As expected, the bud of a typical CDC1 cell almost always contains Sec7p–GFP (not shown). By contrast, the bud of a typical cdc1-304 mutant cell alternately contains and lacks Sec7p–GFP (Fig 5). This result confirms that the buds of cdc1-304 cells are viable and fits with our hypothesis that Cdc1p function is needed to retain late Golgi elements in the bud.

View larger version (88K): [in this window] [in a new window]   Figure 5. The small buds of cdc1-304 cells repeatedly lose and regain late Golgi elements. Shown are merged fluorescence and transmitted light projections of a representative budded cdc1-304 cell, which had been incubated at 37°C for 2 h when imaging was initiated. These selected frames from the time series demonstrate that the bud alternately contains and lacks detectable Sec7p–GFP fluorescence. Bar, 2 µm.

Sec7p–GFP Inheritance Is Inhibited by the myo2-66 Mutation
We conjectured that both the actin-dependent transport and the retention of Golgi elements might involve Myo2p, an essential type V myosin (Johnston et al. 1991 ). Myo2p has been implicated in the transport of organelles toward sites of polarized growth (Pruyne and Bretscher 2000 ). Moreover, Myo2p shows a weak concentration in the bud even in LatA-treated cells (Ayscough et al. 1997 ).

To test whether Myo2p functions in Golgi inheritance, we took advantage of the well-characterized myo2-66 allele, which encodes a protein with a point mutation in the actin-binding motor domain (Lillie and Brown 1994 ). At 23°C, actin organization in myo2-66 cells is essentially normal (Johnston et al. 1991 ; Rossanese, O.W., unpublished observations), but vacuolar inheritance is severely compromised (Hill et al. 1996 ). We introduced the myo2-66 allele into our standard yeast strain and examined cells grown at 23°C. Like cdc1-304 cells, myo2-66 cells exhibit pronounced defects in the inheritance of vacuoles and Sec7p–GFP (Fig 6A and Fig B). These findings suggest that Myo2p participates in the transport and retention of late Golgi elements.

View larger version (16K): [in this window] [in a new window]   Figure 6. Defective inheritance of vacuoles and Sec7p–GFP in myo2-66 cells. Cultures carrying the wild-type MYO2 gene (strain BGY316; ) or the myo2-66 allele (strain BGY415; •) were grown at 23°C and assayed as in Fig 2 for the inheritance of vacuoles (A) or Sec7p–GFP (B).

Cdc1p and Myo2p Are Required for Normal Inheritance of the Late Golgi Marker Ric1p–GFP
All of the experiments described so far used Sec7p–GFP as the late Golgi marker. Thus, we were concerned that our data might reflect the specific behavior of Sec7p–GFP rather than the general behavior of late Golgi elements. To exclude this possibility, we sought to create a second GFP-labeled marker for the late Golgi apparatus. This task was not straightforward because many late Golgi proteins also localize to endosomes; indeed, Sec7p is one of the few proteins that is thought to be specific for the late Golgi apparatus (Lewis et al. 2000 ). However, Siniossoglou and colleagues 2000 recently reported that Ric1p forms part of a protein complex that partially colocalizes with Sec7p at the late Golgi apparatus. Ric1p–GFP yields a punctate fluorescence pattern in living cells (Fig 7 A). In cdc1-304 and myo2-66 cells, Ric1p–GFP inheritance is significantly reduced during the earliest stages of bud growth (Fig 7 B), although the inheritance defects are somewhat less severe than those observed with Sec7p–GFP (see above). This result confirms that Cdc1p and Myo2p play a general role in the inheritance of late Golgi elements.

View larger version (47K): [in this window] [in a new window]   Figure 7. Creation of a second late Golgi marker. (A) Representative cells expressing RIC1–GFPx3. Shown is a merged DIC and fluorescence image. (B) Inheritance of Ric1p–GFP in wild-type and mutant cells. As described in the legend to Fig 3 B, a wild-type strain (), a cdc1-304 strain (•), and a myo2-66 strain () were assayed for the inheritance of Ric1p–GFP. The wild-type and cdc1-304 strains were grown at 23°C and then shifted to 37°C for 1 h before fixation. The myo2-66 strain was maintained at 23°C before fixation, but the myo2-66 data can be compared with the wild-type data because Golgi inheritance in wild-type cells is unaffected by shifting to 37°C for 1 h (not shown). The inheritance of Ric1p–GFP is significantly inhibited by the cdc1-304 and myo2-66 mutations. Bar, 2 µm.

Early and Late Golgi Elements Are Inherited by Distinct Pathways
How are early Golgi elements inherited in S. cerevisiae? Here we are defining the early Golgi as the cis- and medial-Golgi cisternae that do not label with Sec7p–GFP. To monitor the inheritance of early Golgi elements, we created two additional GFP-labeled marker proteins. For the first marker, GFP was linked to the COOH terminus of Sec21p, which is the -COP subunit of the COPI coatomer (Hosobuchi et al. 1992 ). Vertebrate COPI is present at all levels of the Golgi stack except possibly the trans-most cisternae (Oprins et al. 1993 ; Orci et al. 1997 ; Ladinsky et al. 1999 ). Several of the vertebrate COPI subunits are found on both Golgi membranes and endosomes, but -COP is restricted to the Golgi complex (Whitney et al. 1995 ; Gu and Gruenberg 1999 ), suggesting that Sec21p should be a specific marker for the Golgi in yeast. Sec21p–GFP labels multiple punctate structures per cell (Fig 8 A) and exhibits partial colocalization (not shown) with the medial-Golgi marker Mnt1p/Kre2p (Jungmann and Munro 1998 ; Lussier et al. 1995 ). In addition, Sec21p–GFP exhibits partial colocalization with Sec7p (Fig 8 B). Thus, Sec21p–GFP marks both early and late Golgi elements. For the second additional Golgi marker, GFP was fused to the NH₂ terminus of Ypt1p, a small GTPase that regulates membrane traffic at early stages of intra-Golgi transport (Segev et al. 1988 ; Preuss et al. 1992 ; Jedd et al. 1995 ). GFP–Ypt1p labels multiple punctate structures per cell (Fig 8 A). As expected, GFP–Ypt1p exhibits no significant colocalization with Sec7p (Fig 8 B), confirming that GFP–Ypt1p exclusively marks the early Golgi.

View larger version (34K): [in this window] [in a new window]   Figure 8. Creation of two additional GFP-labeled Golgi markers. (A) Representative cells expressing SEC21-GFPx3 or GFP-YPT1. Shown are merged DIC and fluorescence images. (B) Double label immunofluorescence of Sec7p with either Sec21p–GFP or GFP–Ypt1p. Fixed cells were labeled with polyclonal anti-Sec7p antibody followed by Rhodamine red-X–conjugated anti–rabbit antibody (red) and with monoclonal anti-GFP antibody followed by Cy2-conjugated anti–mouse antibody (green). As shown in the merged images, Sec7p shows partial colocalization with Sec21p–GFP but no significant colocalization with GFP–Ypt1p. Bars, 2 µm.

Like late Golgi markers, Sec21p–GFP and GFP–Ypt1p are present in most of the small buds during normal growth (Fig 8 A) or after LatA treatment (not shown). However, as judged by the plus–minus visual assay, Sec21p–GFP and GFP–Ypt1p are inherited normally in strains carrying the cdc1-304 allele (Fig 9). In the case of Sec21p–GFP, the cdc1-304 mutation presumably blocks the inheritance of Sec21p–GFP-containing late Golgi elements but not of Sec21p–GFP-containing early Golgi elements. The myo2-66 mutation has only a mild inhibitory effect on Sec21p–GFP inheritance and has no effect on GFP–Ypt1p inheritance (Fig 9). These data suggest that early Golgi elements can localize to the bud independently of Cdc1p and Myo2p. We conclude that in S. cerevisiae, early Golgi elements and late Golgi elements are inherited by distinct pathways.

View larger version (16K): [in this window] [in a new window]   Figure 9. Inheritance of early Golgi markers in wild-type and mutant cells. As described in the legend to Fig 3 B, wild-type strains (), cdc1-304 strains (•), and myo2-66 strains () were assayed for the inheritance of Sec21p–GFP (A) and GFP–Ypt1p (B). The wild-type and cdc1-304 strains were grown at 23°C and then shifted to 37°C for 1 h before fixation, whereas the myo2-66 strains were maintained at 23°C before fixation (see Fig 7). The inheritance of Sec21p–GFP is unaffected by the cdc1-304 mutation and is inhibited only slightly by the myo2-66 mutation, whereas the inheritance of GFP–Ypt1p is not affected by either mutation.

One possible mechanism for early Golgi inheritance would be the de novo formation of Golgi cisternae from ER membranes. Previous electron microscopy data indicated that peripheral ER membranes are present in the bud early in the cell cycle (Preuss et al. 1991 ). We have verified this observation using fluorescence microscopy. To visualize the ER, the Kar2p presequence was linked to GFP, and a COOH-terminal HDEL tetrapeptide was added to retain the protein in the ER lumen (Pelham 1995 ; Zheng and Gierasch 1996 ). GFP–HDEL highlights the nuclear envelope as well as peripheral ER elements (Fig 10 A). We find that >95% of the small buds contain GFP–HDEL from the earliest stages of bud development. To confirm that bud-localized ER membranes are capable of functioning as tER, we generated cells in which the COPII coat protein Sec13p (Pryer et al. 1993 ) was tagged with GFP. Sec13p-GFP labels multiple fluorescent specks (Fig 10 B) that presumably represent COPII vesicles budding throughout the ER network (Rossanese et al. 1999 ). Like GFP–HDEL, Sec13p-GFP is visible in virtually all of the buds. Hence, it is plausible that the ER membranes present in the bud could generate early Golgi elements. As predicted by this model, ER and tER inheritance are unaffected by the cdc1-304 mutation (Fig 10) or the myo2-66 mutation (not shown). This observation may explain why early Golgi elements are inherited efficiently in cdc1-304 cells and myo2-66 cells.

View larger version (125K): [in this window] [in a new window]   Figure 10. The ER and tER are inherited normally in cdc1-304 cells. (A) Fluorescence images of wild-type (BGY418) and cdc1-304 (BGY419) strains expressing GFP–HDEL. This protein marks the nuclear envelope as well as peripheral ER membranes. Cells were grown at 23°C and then shifted to 37°C for 1 h before fixation. (B) Merged DIC and fluorescence images of wild-type (BGY318) and cdc1-304 (BGY110) strains expressing SEC13-GFP. This fusion protein marks the nascent COPII vesicles that define the tER. Both the ER and the tER localize to small buds with undiminished efficiency in the cdc1-304 mutant. Bars, 2 µm.

	Discussion

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

In budding yeasts, organellar inheritance is not directly coupled to cell division. This feature has made S. cerevisiae a productive system for studying mitochondrial and vacuolar inheritance (Yaffe 1999 ; Catlett and Weisman 2000 ). A portion of the mitochondrial and vacuolar material present in the mother cell is transferred into the bud. However, when vacuolar transfer is inhibited, the daughter cells still acquire a vacuole, probably via the fusion of Golgi-derived vesicles with endocytic vesicles (Hill et al. 1996 ; Gomes De Mesquita et al. 1997 ). This type of de novo formation of compartments may be a general feature of the exocytic and endocytic pathways (Glick and Malhotra 1998 ). Thus, the inheritance of various yeast organelles involves either transfer from the mother cell into the bud, de novo formation in the bud, or both.

Inheritance of Late Golgi Elements
Golgi inheritance has not previously been analyzed at the molecular genetic level in yeast. The inheritance of the vertebrate Golgi has been studied (Lowe et al. 1998 ; Thyberg and Moskalewski 1998 ), but the vertebrate Golgi differs from the S. cerevisiae Golgi in several ways. First, the vertebrate Golgi is organized into stacks. Second, the vertebrate Golgi breaks down during mitosis, whereas the S. cerevisiae Golgi remains intact throughout the cell cycle (Preuss et al. 1992 ; Lowe et al. 1998 ). Third, vertebrate Golgi dynamics are strongly influenced by microtubules, whereas in S. cerevisiae, microtubules have not been implicated in the dynamics of any organelle except the nucleus (Botstein et al. 1997 ). Consistent with this latter observation, we find that depolymerization of microtubules in S. cerevisiae has no detectable effect on the distribution or inheritance of Golgi elements (Fig 1 C; data not shown).

How might Golgi cisternae in S. cerevisiae localize to the bud? One obvious possibility is actin-dependent transport from the mother cell into the bud (Preuss et al. 1992 ). Actin is known to direct the transport of secretory vesicles and other structures to sites of polarized growth (Botstein et al. 1997 ). However, another possibility is that Golgi cisternae grow out of peripheral ER membranes, which are present in the bud from an early stage in bud development (Preuss et al. 1991 ). We set out to test whether one or both of these mechanisms contributes to Golgi inheritance in S. cerevisiae. Most of our experiments used a Sec7p–GFP fusion protein as the Golgi marker (Seron et al. 1998 ). Sec7p is an abundant component of late Golgi cisternae (Franzusoff et al. 1991 ; Lewis et al. 2000 ), and the Sec7p–GFP fusion gives a robust fluorescence signal.

Sec7p–GFP fluorescence is often concentrated at sites of polarized growth, but only in cells that contain an intact actin cytoskeleton (Fig 1). A simple model to explain these observations is that late Golgi elements are transported along actin cables by a myosin motor. Yet, surprisingly, when actin is depolymerized with LatA, some Sec7p–GFP is still present in the small buds (Fig 2). In other words, disrupting the actin cytoskeleton reduces but does not abolish the inheritance of late Golgi elements. These data suggest that late Golgi elements are transported into the bud along actin cables but that a subset of the late Golgi elements can localize to the bud, even when actin cables have been eliminated using LatA (Fig 11 B). The LatA-resistant inheritance mechanism might be independent of actin, or it might involve residual actin structures that are resistant to depolymerization by LatA (Karpova et al. 2000 ).

View larger version (52K): [in this window] [in a new window]   Figure 11. Model for Golgi inheritance in S. cerevisiae. (A) Inheritance of early Golgi elements. The ER comprises the nuclear envelope plus peripheral ER membranes. COPII vesicles bud throughout the ER network, thereby generating early Golgi cisternae in both the mother cell and the bud. The inheritance of early Golgi elements requires ER inheritance but does not directly require actin cables, Myo2p or Cdc1p. (B) Inheritance of late Golgi elements. Dimeric Myo2p molecules bind to late Golgi cisternae and transport these cisternae along actin cables into th