Ubiquitin conjugation signals for selective protein degradation by the proteasome. In eukaryotes, ubiquitin is encoded both as a monomeric ubiquitin unit fused to a ribosomal gene and as multiple ubiquitin units in tandem. The polyubiquitin gene is a unique, highly conserved open reading frame composed solely of tandem repeats, yet it is still unclear why cells utilize this unusual gene structure. Using the Saccharomyces cerevisiae UBI4 gene, we show that this multi-unit structure allows cells to rapidly produce large amounts of ubiquitin needed to respond to sudden stress. The number of ubiquitin units encoded by UBI4 influences cellular survival and the rate of ubiquitin-proteasome system (UPS)-mediated proteolysis following heat stress. Interestingly, the optimal number of repeats varies under different types of stress indicating that natural variation in repeat numbers may optimize the chance for survival. Our results demonstrate how a variable polycistronic transcript provides an evolutionary alternative for gene copy number variation.
Timely degradation of proteins by the ubiquitin-proteasome system (UPS) is key to many physiological processes and stress survival1,2,3,4. Heat stress induces protein misfolding and aggregation, and rapid clearance of misfolded proteins is essential for cells to survive and re-initiate cell division. In eukaryotes, the heat shock (HS) response involves the upregulation of stress-induced genes (e.g., chaperones) and increased ubiquitination of cytosolic proteins5,6,7 thereby increasing the demand for ubiquitin moieties.
Ubiquitin is present in the cell as free and protein-bound ubiquitin pools, which are highly dynamic and interchangeable. Their equilibrium is maintained through tight transcriptional regulation of the various components of the UPS. In eukaryotes, ubiquitin is always encoded by a gene fusion8, 9. In yeast, three genes encode ubiquitin as a monomeric ubiquitin unit fused to ribosomal proteins: RPL40A (UBI1); RPL40B (UBI2); and RPS31 (UBI3)8, 10. One additional ubiquitin gene, UBI4, encodes multiple ubiquitin units in tandem11, 12. Each of these fusion genes is transcribed as a single transcript and translated into ubiquitin precursors (i.e., a ubiquitin moiety fused to a ribosomal protein or to another ubiquitin) that are subsequently cleaved by specialized proteases called deubiquitinating enzymes (DUBs) to release mature ubiquitin monomers13. This process constitutes the de novo ubiquitin synthesis. Some DUBs, such as Ubp1, can also cleave unanchored polyubiquitin chains and thus further contribute to the total cellular ubiquitin levels14. Ubiquitin monomers can also be regenerated by DUBs from anchored polyubiquitin chains that are released from ubiquitinated proteins before degradation by the proteasome10.
As UBI1, UBI2, and UBI3 encode ribosomal proteins, their expression correlates with cell growth rate, and is repressed by stress conditions. Conversely, expression of the polyubiquitin UBI4 gene is stress-inducible and increases after heat stress, upon exposure to DNA-damaging agents, under oxidative stress, in stationary phase and in conditions of zinc deficiency11, 15,16,17. This regulation makes UBI4, a gene composed solely of tandem repeats, the main source of de novo ubiquitin synthesis under stress conditions.
Tandem repeats are known to be highly unstable as they frequently induce DNA replication slippage or intragenic recombination that lead to the addition or removal of repeat units. Yet many tandem repeats occur within regulatory or coding sequences where their variability can lead to beneficial functional changes18,19,20. The eukaryotic polyubiquitin gene constitutes a special example of a tandem repeat since the entire open reading frame of this gene is composed of several repeats of a DNA sequence that encodes one ubiquitin unit8. Despite extensive research on the UPS and its multiple components, the advantages of such a multi-unit gene structure, and whether the (natural) variation in the number of ubiquitin-coding units affects cell physiology have not been previously investigated.
Using the Saccharomyces cerevisiae polyubiquitin gene UBI4 as a model and a combination of genetic and biochemical approaches, we show that the eukaryotic polyubiquitin gene is evolutionarily unstable and that variation in the number of ubiquitin units underlies variation in survival capacity after stress. Interestingly, we found that different UBI4 repeat numbers are optimal under different stress conditions. We also show that the UPS-mediated degradation kinetics of ubiquitinated proteins during HS depends on the number of ubiquitin repeats. The multiunit structure of the polyubiquitin gene thus constitutes an elegant alternative to gene copy number variation where the number of encoded ubiquitin units allows tuning of the UPS activity, protein homeostasis, and cellular survival during stress.
Ubiquitin repeat number varies between and within species
The polyubiquitin gene is transcribed and translated into a multiunit ubiquitin precursor that is subsequently cleaved by specific DUBs to yield monomeric ubiquitin moieties13 (Fig. 1a). The repetitive nature of the polyubiquitin gene is conserved throughout the eukaryotic lineage8, 21,22,23,24 (Fig. 1b). We surveyed > 1000 eukaryotic polyubiquitin-coding sequences in the Uniprot database and found extensive variability in the polyubiquitin repeat number between species and strains (Fig. 1c and Supplementary Data 1). In several lineages, including humans and mice, the polyubiquitin gene underwent a duplication event (Fig. 1b) and the resulting paralogs acquired different expression patterns and functional roles22, 24,25,26,27. A comprehensive genome analysis revealed that one paralog (often the shortest variant) shows little to no changes in repeat number, whereas the longer variant shows extensive repeat number variability (Fig. 1b, c and Supplementary Data 1).
To determine the range of repeat number variability in the polyubiquitin gene within closely related species and strains, we PCR-amplified the UBI4 gene in 98 natural strains and species of Saccharomyces yeasts selected to represent the natural diversity of this genus28, 29 (Supplementary Data 2 and Fig. 1d). In the strains for which PCR amplification generated multiple bands, the exact gene size (and hence UBI4 repeat number) was resolved by Southern blot analysis to rule out slippage events during PCR amplification (Fig. 1e). The UBI4 allele coding for five units was observed in 53% of the tested strains (Fig. 1f). The results uncover a remarkably high variability in the number of ubiquitin-coding units across the UBI4 genes in the Saccharomyces genus, with some of the diploid or polyploid strains containing UBI4 alleles of different lengths (Supplementary Data 2). Alleles containing only 2 repeats were always found to be heterozygous, with one allele containing 2 repeats and the other(s) containing at least 4. This suggests that there might be selection against having only a few UBI4 repeats.
UBI4 repeat number influences HS survival
To investigate whether the natural variability in UBI4 repeat number influences cellular fitness in conditions where fast protein turnover is critical, we measured the survival of a set of natural Saccharomyces strains after a sudden temperature shift from 30 to 43 °C, a condition known to induce the UBI4 gene11, 17. We find that survival rates under these conditions seem to be affected by the strains’ UBI4 repeat number, rather than the ecological or industrial niche from which the different yeast strains were isolated (Fig. 2a, right panel). Specifically, strains with at least one short UBI4 allele (2 or 3 units) have significantly lower survival rates than the ones with longer alleles (4 or 5 units; Fig. 2a). Interestingly, strains containing a UBI4 allele with 7 units display low HS survival indicating that more repeat units do not directly correlate with HS survival (Fig. 2a). It should be noted that out of the 98 natural strains tested, only 3 strains contained a UBI4 allele with 7 repeats (Fig. 1f), possibly pointing to an unfavorable effect of this allele.
We believe this effect is connected to the ubiquitin repeat number especially given a notable example with 2 genetically related strains (strains Y335 and Y342; Supplementary Data 2 and ref. 29). Both strains are used for ale beer production, but have different UBI4 repeat numbers (2 vs. 4) and show extremely different survival rates during heat stress (15% vs. 79%).
Many industrial and wild strains are polyploid, and can thus carry several alleles of UBI4 per strain that can each differ in their number of repeats. The presence of multiple alleles of varying repeat length in these polyploids can obscure the effect of UBI4 repeat number on HS survival. However, we observe a similar, statistically significant difference in survival rates between 14 haploid derivatives of industrial or wild S. cerevisiae strains. Strains having an allele with 3 units showed a significant reduction in heat stress survival compared to those containing an allele with 5 units (Fig. 2b).
To further disentangle the effect of variation in UBI4 repeat number on HS survival from the effect of variation in ploidy and genetic background, we generated isogenic variants of the S. cerevisiae S288c lab strain that only differ in the number of UBI4 repeats (Fig. 1d, framed section). These strains allowed us to evaluate in a more direct way if differences in the number of ubiquitin-coding units of UBI4 affect HS survival. After a sudden temperature shift (30 to 44 °C), survival rates first increase with increasing UBI4 repeat number, reaching a maximum for the variant with 3 repeats before decreasing again (Fig. 2c). These results suggest that the number of ubiquitin moieties synthesized from the UBI4 gene directly influences cell survival following a sudden HS.
To rule out ubiquitin-independent effects responsible for the fitness differences, we created a one-repeat UBI4 variant that contains a Lys48Arg mutation that prevents this moiety from being used in polyubiquitination reactions. This mutant has a survival rate comparable to the mutant with a complete UBI4 deletion and significantly lower than the strain with an intact one-repeat UBI4 allele (Supplementary Fig. 1). This indicates that the survival rates after HS are directly dependent on ubiquitin produced from the UBI4 gene.
To determine if our observed phenotypes were in fact a dose-dependent consequence of multiple units, we created mono-ubiquitin copy number variants. In these variants, we replaced the UBI4 gene by one or two copies (in tandem) of a single ubiquitin moiety, each controlled by its own promoter (Fig. 2d). A third ubiquitin moiety was inserted at a neutral genomic location (depicted by the yellow overhangs in Fig. 2d) to obtain a variant with 3 copies of a single ubiquitin unit (Fig. 2d). The survival of these variants after a sudden HS also increases with the number of mono-ubiquitin moieties (Fig. 2d), similar to what we observe with the tandem repeat number variants (Fig. 2c). These results suggest that having multiple ubiquitin-encoding repeats within one gene or multiple copies of a mono-ubiquitin-coding gene may increase the cells’ capacity to generate the large amounts of ubiquitin needed for the proteome to quickly adapt to the HS. Our data also suggest that having multiple copies of a mono-ubiquitin-encoding gene can (partially) recapitulate the HS survival phenotype of a strain that has a multiunit gene structure (polyubiquitin). However, it should be noted that HS survival of strains with a multiunit gene structure is often slightly better compared to strains encoding multiple copies of mono-ubiquitin.
Optimal UBI4 repeat number is condition-specific
Considering the variability in natural UBI4 repeat number, we further investigated the possible role of UBI4 repeat number variation in surviving other types of stress, using the isogenic UBI4 repeat variants (Fig. 2c). Oxidative stress and nitrogen starvation have both been linked to UBI4, as ubi4 null mutants display increased sensitivity to both types of stress15. When the isogenic UBI4 repeat number variants were grown on a nitrogen-starved medium at an elevated temperature, the short variants (≤2 repeats) showed reduced fitness relative to the long variants (≥3 repeats; Supplementary Fig. 2). Interestingly, under these conditions, the UBI4 allele encoding 5 repeats gives the clearest growth advantage.
A similar trend was seen when cells were exposed to oxidative stress. While all strains displayed a reduced maximal growth rate and increased recovery (lag) time under oxidative stress conditions compared to no stress conditions (YPD, Yeast extract, Peptone and Dextrose) (Supplementary Fig. 3), strains containing 5 UBI4 repeats reproducibly grew better under oxidative stress compared to UBI4-null or single-repeat strains (higher growth rate in the presence of 2.5 mM paraquat; unpaired t-test, two-sided p-values < 0.05). Although 3 repeats appeared optimal for HS recovery, under oxidative stress these strains took significantly longer to recover than single-repeat strains (longer lag time; unpaired t-test, two-sided p-value = 0.0461).
A recent study showed that a 2-repeat UBI4 variant is less fit in zinc-deficient conditions relative to a 5-repeat variant16. In line with our findings, a recent large-scale study also showed that the exact expression level of a gene required for optimal fitness is highly condition-specific30. Taken together with our results, the variation in the “best” repeat number demonstrates that there is no single number of repeats in UBI4 that is optimal in all possible environments. Rather, variation in UBI4 repeat number is likely an evolutionary “tuning knob” that allows strains to optimize their stress-induced ubiquitin system, with different repeat numbers being optimal under different stress conditions (type, severity, and duration).
UBI4 is main source of de novo ubiquitin during heat stress
In S. cerevisiae, the majority of ubiquitin is provided by the monomeric UBI1 (RPL40A), UBI2 (RPL40B), and UBI3 (RPS31) genes under physiological growth conditions, whereas the polyubiquitin gene UBI4 has been shown to be the major source of ubiquitin during stress11, 17. To check if differences in transcription of the UBI4 gene could explain the differences in survival observed for the different UBI4 repeat number variants (Fig. 2), we used real-time quantitative PCR (RT-qPCR; see Supplementary Information for more details on specific primer design—we measured the number of transcripts from each UBI4 repeat variant, rather than the total number of ubiquitin moieties). We monitored the transcriptional response of all ubiquitin-coding genes in the UBI4 repeat number variants during a time course after the cells were shifted from 30 to 44 °C. We observe that during this sustained HS, UBI4 induction is quick and transient, reaching a maximum after 30 min, confirming previous reports17 (Fig. 3a). UBI4 transcripts in all the variants increase to a similar level after the cells are shifted to a higher temperature, except for the 1-repeat variant whose induction continues to increase after 30 min (Fig. 3a). Surprisingly, the steady-state expression of UBI4 before the heat stress (at 30 °C) differs between the repeat variants and reveals an anticorrelation between the UBI4 mRNA levels and its number of ubiquitin repeats (Fig. 3a, inset). For example, UBI4 transcripts are ~ 7-fold higher in the 1-repeat variant and ~ 2.5-fold higher in the 2-repeat variant relative to the wild type (5 repeats). These observations suggest that a basal level expression of UBI4 gene is necessary for maintaining adequate ubiquitin pools in non-stressed conditions and therefore UBI4 likely also plays a role in physiological protein homeostasis in S. cerevisiae, with cells that contain fewer UBI4 repeats compensating for the lack of ubiquitin by increasing basal UBI4 expression.
The ribosomal-fusion UBI1, UBI2, and UBI3 genes are downregulated during HS and their expression follows the opposite trend compared to UBI4 (Fig. 3b). This agrees with previous reports showing that ribosomal genes are downregulated during stress31. Importantly, we find no significant differences in the ribosomal-fusion ubiquitin transcripts (UBI1-3) between the UBI4 repeat variants (Fig. 3b). Taken together, these results confirm that during stress conditions, the bulk of ubiquitin is provided by UBI4 with no or very little contribution from UBI1-3. Moreover, our data suggest that the main contribution to differences in HS survival of the UBI4 variants arises from differences in the amount of ubiquitin moieties generated from the UBI4 gene (see also below).
UBI4 repeat number affects UPS activity during heat stress
Although there are no significant differences in the number of mRNA ubiquitin transcripts in the UBI4 variants with 2, 3, or 5 repeats during HS (Fig. 3), these transcripts are of different length and encode different numbers of ubiquitin moieties. Therefore, part of the difference in HS survival between these UBI4 repeat variants could potentially be explained by differences in the overall number of ubiquitin moieties present in the cell. To examine the effects of differential ubiquitin production from the UBI4 gene on global ubiquitination levels, we extracted soluble proteins from the UBI4 variants at multiple time points during a HS and measured total ubiquitination by western blot (Supplementary Fig. 4). This type of analysis is qualitative and only has the power to resolve large differences in total polyubiquitination yet we clearly observe less polyubiquitination of soluble proteins in the UBI4 variant with 0 and 1 repeat relative to the higher repeat variants. Polyubiquitination levels at a physiological temperature were comparable across all UBI4 variants (HS 0 min) and after 30 min of HS, there is clearly more polyubiquitin in strains with ≥2 repeats. Since this method cannot resolve minor differences, we cannot exclude the possibility of variation in polyubiquitination within the higher (2–5) repeat variants.
Proteasomal degradation dynamics can be influenced by several factors, including the configuration of the ubiquitin chains on the protein substrate as well as the total number of ubiquitin moieties present on the substrate32, 33. To unravel possible differences in the UPS activity between UBI4 repeat variants and check whether lower polyubiquitination in the short UBI4 variants results in slower substrate degradation, we employed a well-established, quantitative assay to measure UPS-dependent protein degradation in single cells using a modified green fluorescent protein (GFP)34, 35. We measured fluorescence in UBI4 repeat variants expressing UbG76V-GFP, a substrate for ubiquitin-proteasome-dependent proteolysis, or the stable Ub-M-GFP as a control, after a temperature shift from 30 to 44 °C (Fig. 4a). We determined the turnover rates of ubiquitinated GFP, and by extension the UPS activity, by calculating the frequency of the remaining fluorescent cells over the total number of cells at multiple time points during the HS (Fig. 4a and Methods for details). Whereas UbG76V-GFP was degraded with a half-life of ~ 2 h in cells containing a 5-repeat UBI4 during HS, its half-life gradually became longer with decreasing UBI4 repeat number (Fig. 4b). In contrast, the levels of the stable form of GFP (Ub-M-GFP) were the same for all strains and were relatively unchanged throughout the course of the HS (Fig. 4b, lower panel).
To ensure that the observed differences in half-life were not due to differences in substrate (GFP) expression, we measured the levels of GFP-mRNA by RT-qPCR. mRNA levels remain virtually unchanged during the HS experiment, and are also similar across all the UBI4 repeat variants (Supplementary Fig. 6 and Supplementary Data 4). Moreover, degradation of UbG76V-GFP was drastically slowed down upon proteasome inhibition by addition of MG132 (Supplementary Fig. 7), further indicating that the degradation of UbG76V-GFP takes place via the proteasome. It is also interesting to note that the strain with the fastest protein turnover (5-repeat UBI4) does not display the best survival after sudden HS (Fig. 2c). This underscores that faster protein turnover is not necessarily better for cellular fitness (see also Discussion).
Interestingly, the steady-state levels of UbG76V-GFP at a physiological temperature (30 °C) negatively correlated with the number of UBI4 repeats (Fig. 4c). Since growth profiles at 30 °C are comparable between the UBI4 variants (Supplementary Fig. 8), we do not expect any noticeable contribution of protein dilution. The differences at this physiological temperature therefore likely result from variation in UPS-mediated proteolysis, with variation in UBI4 repeat number potentially affecting proteasome activity even at physiological temperatures.
Many studies have highlighted the critical roles of ubiquitin homeostasis for normal cellular physiology and stress response. In mice, the failure to recycle ubiquitin from proteasomal substrates results in synaptic dysfunction36 and deletion of either polyubiquitin gene paralog underlies severe pathological phenotypes26, 27. Additionally, alteration in protein half-life can result in developmental abnormalities, neurodegeneration, and cancer37. In yeast, depletion of the free mono-ubiquitin pool renders the cells susceptible to translational inhibition38. But why would cells need a polycistronic ubiquitin gene to survive stressful conditions? What are the advantages of a multiunit gene structure? Does the natural variability in the number of ubiquitin-coding units affect cell physiology and stress responses?
Using a combination of genetic and biochemical approaches, we sought to address this gap in our understanding of ubiquitin biology. We show that the variation in the number of ubiquitin repeats encoded by the polyubiquitin gene (UBI4) underlies variation in stress resistance. The UBI4 variants with short repeat number (≤ 2 repeats) show increased sensitivity to a wide range of stresses, whereas the longer repeat alleles provide increased resistance to stress. Interestingly, this effect on stress resistance is highly condition-specific, indicating that certain alleles are optimal for fitness in one stress condition, but not in another.
Our results also indicate that repeat variation in the polyubiquitin gene can tune the degradation kinetics of ubiquitinated proteins during stress. Short UBI4 repeat variants display a very slow turnover of ubiquitinated substrates. Gradual increases in the number of UBI4 units result in faster proteolysis of ubiquitinated substrates (Fig. 4b). In other words, the activity of the UPS in stress conditions, and consequently the clearance of misfolded proteins, can be tuned by the amount of ubiquitin produced from the polyubiquitin gene. Our study thus adds another factor that can underlie variation in the activity of the UPS during stress—namely variation in the polyubiquitin gene repeat number—in addition to other factors recently described39.
The natural variation in the number of ubiquitin moieties encoded by the polyubiquitin gene could thus affect the proteome half-life dynamics in living cells under stress (e.g., heat, starvation, and oxidative stress) and subsequently play a role in stress resistance and survival. Our data also suggest that variation in the number of UBI4 ubiquitin-coding units can affect proteostasis under non-stress conditions (Fig. 4c).
In sum, our study takes an in-depth look the physiological effects of changes in unit number of the polyubiquitin gene. Our results thus provide a distinct example of how a eukaryotic transcript that contains a tandem repeat of a coding unit serves as an elegant alternative for gene copy number variation, enables cells to quickly produce more copies of a specific open reading frame. Moreover, given the frequent replication slippage or intragenic recombination events that occur at tandem repeat sites (events that are less frequent if the copies would be encoded at different locations spread across the genome), it seems plausible that such a repetitive gene is highly variable and “evolvable”, providing cells with an opportunity to quickly evolve novel stress-induced polyubiquitin gene alleles that result in optimal tuning of internal ubiquitin levels in changing conditions or niches.
HS survival assays
To quantify survival rates after HS, we grew the cultures first in YPD at 30 °C till OD600 = 3–4, diluted them to OD600 = 0.1 in SC (Synthetic Complete) medium containing 2% glucose and transferred 50 μl to a thermocycler for the HS period (4 h). Using the gradient function of the thermocycler we could induce a rapid shift from a physiological growth temperature (30 °C) to different heat stress temperatures (38 to 45 °C) in parallel on multiple samples. We calculated the survival rates (at a given temperature) by dividing the number of colony-forming units obtained for each sample before and after the temperature switch.
Southern blotting was performed using a standard protocol40 on 10 μg of gDNA isolated using the Genomic tip 100/G kit (Qiagen). The blots of NdeI-/EcoRI-digested gDNA were hybridized with a digoxigenin (DIG)-labeled probe prepared by PCR amplification of a UBI4 coded ubiquitin moiety using primers 4028–4029, gDNA from RG525, and the PCR DIG Probe Synthesis kit (Roche).
For nitrogen starvation assays, overnight cultures grown in YPD were normalized to OD600 = 1 in water and 10-fold serially diluted. Ten microliters of each dilution were spotted onto synthetic low-ammonia dextrose plates (nitrogen-poor medium) and incubated at 37 or 41 °C.
For oxidative stress assays, UBI4 repeat variants were grown in YPD to OD600 = 0.1. These cultures were used to inoculate fresh YPD in the presence and absence of 2.5 mM paraquat (Sigma Aldrich). Growth was monitored at 600 nm using a Bioscreen C (Growth Curves, USA) maintained at 30 °C with continuous shaking for 30 h. Maximal growth rate and lag time were calculated in accordance with Swinnen et al.41 using an in-house-built script in R similar to that described by New et al.42. Briefly, lag times were calculated from the growth data using R. First, the optical density (OD) values were subtracted by the background values of wells containing no culture, and the resulting observed ODs (ODobs) were corrected to account for the nonlinearity between cell density (ODcor) and observed OD at higher cell densities (using the formula ODcor = ODobs + 0.449(ODobs)2 + 0.191(ODobs)3 as in ref. 43). Next, the growth rates were calculated by taking the discrete first derivate of the natural logarithm of ODcor vs. time, and smoothening this using a smoothing spline (R function smooth.spline with spar = 0.2). From these data, the maximum growth rate was calculated as the average of the five highest values. The lag time could then be calculated as the time corresponding to the intersection point between two lines on an OD vs. time graph. The first line is an exponential curve that is extrapolated from the point of maximum growth rate and the second line is an horizontal line crossing the vertical axis at the initial OD41.
For growth assays in glucose, UBI4 repeat variants were grown overnight in YPD. The next day, these cultures were used to inoculate fresh YPD. Growth was monitored at 600 nm using a Bioscreen C (Growth Curves) maintained at 30 °C with continuous shaking.
Real-time quantitative PCR
To monitor the expression of all ubiquitin-coding genes during HS, we grew biological duplicates of the UBI4 repeat variants overnight till saturation in YPD. We then diluted the cultures to OD600 = 0.1 in 50 ml SC medium containing 2% glucose and grew them at 30 °C till OD600 = 0.5. We then transferred the cultures to a water bath at 44 °C and at 0, 5, 10, 30, and 60 min after the temperature shift we mixed 6 ml cultures with an equal volume of ice-cold water and collected the cells by centrifugation. We extracted total RNA using the standard phenol–chloroform method44 and synthesized cDNA from 1 μg total RNA using the QuantiTect Reverse Transcription kit (Qiagen). RT-qPCR was performed using the StepOnePlus system (Applied Biosystems). To design RT-qPCR primers that allow us to measure the transcripts from each UBI4 repeat variant, rather than the total number of ubiquitin moieties per transcript, we chose primers that specifically anneal to one ubiquitin moiety by taking advantage of the polymorphisms present between the various ubiquitin moieties in the UBI4-coding sequence. We verified the specificity of the primers by using various concentrations of gDNA from each UBI4 variant. We obtained CT values that were proportional to the concentration of gDNA used and were similar for the UBI4 repeat variants. UBI4 expression was normalized to the expression of the ACT1 gene. To account for differences between RT-qPCR runs and in order to compare trends between different time points, we first normalized to the CT signal from the same amount of gDNA present in each run. We then calculated the ratio of the normalized values to obtain the relative expression levels. Primers used for RT-qPCR are listed below.
To assess polyubiquitination levels in the UBI4 repeat variants during HS, overnight-saturated cultures were diluted in 50 ml YPD and grown at 30 °C till OD600 = 0.6–0.8. Before HS, we harvested cells from 10 ml cultures and transferred the remaining cultures to a water bath at 44 °C. At 15, 30, and 60 min after temperature switch, we again harvested cells from 10 ml cultures. Cell pellets were lysed with glass beads in cold lysis buffer (50 mM Tris (pH 7.4), 100 mM NaCl, 1 mM EDTA, 0.1% Triton X-100, and protease inhibitor cocktail (Roche)) in a FastPrep-24 homogenizer (MP Biomedicals). Extracts were cleared by centrifugation (10 min, 14,000 r.p.m. at 4 °C) and protein concentrations were measured by the Bradford assay (Protein Quantification kit, Sigma-Aldrich). Total proteins (5 μg) were separated by 10–20% gradient gels (Life Technologies) using a Tricine-based buffer, followed by transfer to polyvinylidene difluoride membranes. Blots were incubated with mouse anti-ubiquitin monoclonal antibody MAB1510 (Millipore, 1:2000) followed by incubation with rabbit anti-mouse IgG-horseradish peroxidase-conjugated antibody (ab97046, Abcam, 1:20,000), and western signals were detected using the LumiGLO Ultra Chemiluminescence kit (KPL).
Determination of UPS activity during HS
UBI4 repeat variants carrying plasmids pYES-Ub-M-GFP (stable GFP) or pYES-UbG76V-GFP (ubiquitin fusion degradation substrate)27, 28 (Addgene) were grown for two successive overnights at 30 °C in SC-URA medium containing 2% glucose and then 2% raffinose and 2% galactose. The cultures were next diluted in SC-URA medium containing 2% galactose and grown at 30 °C until midlog phase and then transferred to a water bath at 44 °C. At 0, 10, 30, 60, and 120 min after the temperature shift, 100 µl cultures were centrifuged and cells frozen in 25% glycerol until flow cytometry analysis. Fluorescence of 50,000 cells per sample was measured using a BD Influx flow cytometer equipped with a 488 nm laser and a 530/40 nm filter (GFP). We calculated the frequency of the remaining fluorescent cells over the total population at various time points using the FlowJo software (Tree Star, Inc.). Details on the calculation of the turnover rates are provided in Supplementary Information. A similar setup was used to check effect of proteasomal inhibition, where MG-132 (Sigma) was added to a final concentration of 100 µM.
Determination of UbG76V-GFP turnover rates
To calculate the degradation rates of UbG76V-GFP, we first normalized the remaining fluorescence of each sample at a given time point relative to its initial fluorescence before HS (assigned an arbitrary value of 1). The normalized data were log-transformed and fitted to a straight line using GraphPad Prism. To evaluate the quality of curve fitting, we calculated the goodness of fit of linear regression (R 2) and obtained R 2 > 0.9 in all cases. The average decay rate constant k (i.e., slope) of the best-fit curve from 4 independent measurements was determined and used to calculate the half-life (T 1/2) of GFP as follows:
GFP expression analysis
Cultures were grown essentially as described in ‘Determination of UPS activity during HS.’
Before being subjected to HS, 6 ml cultures were taken as T0 samples, 6 ml cold diethyl pyrocarbonate-treated water was added to each sample. Cell pellets were immediately collected and stored at −80 °C for later RNA isolation. The same sample-taking procedure was performed at different time points during HS.
RNA was isolated using the MasterPure Yeast RNA Purification Kit. The expression levels of GFP were analyzed by RT-PCR using primers PYY144 and PYY145, and the expression levels of ACT1 were analyzed using primers PYY140 and PYY141. A delta-delta Ct method was used (with T0 being the control condition and ACT1 being the control gene) to normalize GFP expression levels. Primers are listed in Supplementary Data 3.
The data supporting the findings of this study are available from the corresponding author upon request.
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Research in KJV lab is funded by an ERC Starting Grant 241426, an HFSP program grant RGP0050/2013, KU Leuven NATAR Program Financing, VIB, FWO, IWT, and the European Molecular Biology Organization Young Investigator Program. M.C.D. is supported by a fellowship from the Belgian American Education Foundation. J.S. acknowledges funding from KU Leuven. K.V. is supported by a FWO postdoctoral fellowship. Research in MR lab is funded by an ERC Starting Grant 26809. M.R. is a Wellcome Trust Research Career Development and Wellcome Beit Prize fellow. Work in the MR lab was supported by the Francis Crick Institute, which receives its core funding from Cancer Research UK (FC001134), the UK Medical Research Council (FC001134), and the Wellcome Trust (FC001134).
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