INTRODUCTION

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Cyclin-dependent protein kinases (CDKs) were first identified as central regulators of the major transitions of the eukaryotic cell division cycle. Their activity is determined by cyclin binding, by both positive and negative regulatory phosphorylation, and by polypeptide CDK inhibitors (40, 41). A single cyclin-dependent kinase subunit associates sequentially with multiple cyclin partners whose abundance fluctuates during the cell cycle (43). Indeed, one aspect of CDK regulation is triggered by the rapid destruction of their cyclin partners (23). Several studies both in yeast and in mammals have demonstrated that cyclins are selectively degraded by the ubiquitin-dependent proteasome pathway (9, 16, 53, 67). Substrates are first marked for degradation by conjugation with several molecules of ubiquitin, a highly conserved 76-amino-acid-long polypeptide that is joined reversibly by a covalent linkage. Usually, ubiquitin molecules are linked tandemly at lysine 48 to form multiubiquitin chains on substrate proteins (47). The resulting ubiquitin chains are in a dynamic state, subject to either further rounds of ubiquitination, ubiquitin removal by deubiquitinating enzymes, or degradation by the 26S proteasome (20). The 26S proteasome is a nuclear and cytosolic multicatalytic proteinase that breaks down targeted substrates to short peptides and recycles the ubiquitin molecules (18).

How proteins are targeted to the ubiquitin-mediated proteasome degradation pathway is not well understood. At least two motifs, which are also found in other ubiquitinated proteins, are necessary for cell cycle cyclin targeting to the ubiquitin proteolytic pathway. In the yeast Saccharomyces cerevisiae, mitotic (Clb1 to Clb4) and S-phase (Clb5 and Clb6) cyclins are targeted by a consensus sequence called the destruction box (16, 24, 42), while targeting of G₁ cyclins (Cln1 to Cln3) requires a carboxy-terminal PEST-rich region (49, 51). Regulation of cyclin destruction has also been shown to be dependent on their associated CDKs (7), and several studies indicated that G₁ cyclin phosphorylation provides a signal that is necessary for their rapid degradation, suggesting that the relevant aspect of PEST sequences might be their richness in CDK phosphorylation target sites rather than their PEST amino acids per se. Indeed, mutations in the Cdc28p kinase consensus phosphorylation sites of G₁ cyclins resulted in their stabilization (28, 68). In summary, phosphorylation of cyclin PEST regions by their associating CDKs triggers their degradation. Thus, expression of a cyclin may be negatively regulated by the same cell cycle machinery that it activates.

C-type cyclins were originally identified in Drosophila melanogaster and humans because they could rescue G₁ cyclin function in yeast (33, 34). Since then, cyclins with significant homology to the cyclin box region of cyclin C have also been found in Schizosaccharomyces pombe (14, 39). Except for a recent study carried out in murine cells (36), there has been no evidence supporting a critical role for C-type cyclins in cell cycle progression. Rather, C-type cyclins seem to activate CDKs involved in the regulation of RNA polymerase II transcription. Unlike cell cycle cyclins, their expression does not fluctuate during the cell cycle (6, 39). The S. cerevisiae genome encodes three C-type cyclins that have been identified as subunits of RNA polymerase II carboxy-terminal domain (CTD) kinases. The RNA polymerase II CTD plays an essential role in mRNA synthesis, and its phosphorylation is a key feature of its function (8). The first CTD kinase, Kin28p, is associated with Ccl1p, a C-type cyclin, and with a third factor, Rig2p (12, 61, 62). This complex, like its human counterpart the Cdk7p kinase complex (37), is a component of the general transcription factor TFIIH (44, 58). Kin28p kinase activity is essential, as it is required for basal transcription (62). The second CDK implicated in CTD phosphorylation is the Srb10p/Ume5p/Ssn3p kinase and its cyclin partner Srb11p/Ume3p/Ssn8p, a kinase pair that is a component of the holoenzyme (35). The Srb10/11 complex is structurally related to mammalian Cdk8p kinase and its associated cyclin C (59). It was first characterized as a regulator of meiosis-specific genes in response to glucose (57). Since then, several studies established that Srb10/11 kinase is implicated in transcription repression of sets of genes (1, 27, 65). Cooper et al. (6) showed that Ume3p cyclin is destroyed during meiosis and when cultures are subjected to heat shock. Mutational analysis identified several regions implicated in Ume3p stability: a PEST-rich region, a destruction box-like motif (RXXL), and the highly conserved cyclin box. Strikingly, this process does not appear to be affected in mutants defective for ubiquitin-mediated protein destruction. Furthermore, in contrast to what has been described for yeast cell cycle cyclins, the CDK activated by Ume3p is not required for the rapid degradation of this cyclin.

The third yeast C-type cyclin is a component of the CTDK-I complex, which was isolated in vitro by its ability to phosphorylate CTD-containing fusion proteins (29). It is composed of three subunits: the CTK1 and CTK2 genes encode a kinase and a C-type cyclin, respectively; the third subunit, Ctk3p, shows no similarity to other known proteins (30, 56). Deletion of any of the CTK genes generates cryosensitive cells. CTDK-I is related to the Srb10/11 kinase complex, although it seems to display a distinct role in transcriptional control (26). In vitro studies carried out with HeLa nuclear extracts have shown that CTDK-I can modulate the elongation efficiency of RNA polymerase II (31). In humans, the closest kinase to Ctk1p is Cdk9p, a CTD kinase that was first described as a positive transcription elongation factor (38). A recent study showed that Cdk9p is associated with a C-type cyclin that also interacts specifically with the human immunodeficiency virus type 1 transactivator protein Tat, which acts to enhance the processing efficiency of RNA polymerase II (66, 69). This finding led the authors to propose that this cyclin might be the TAR RNA-binding cofactor for Tat (66).

C-type cyclins constitute a divergent family of cyclins that display a prime role in RNA polymerase II transcription. Regulation of their expression is poorly documented. The yeast cyclin Ume3p is highly unstable under certain conditions, but how this regulation is achieved remains unknown. To try to understand the regulation of their expression, which probably exhibits specific features, we have studied the expression of Ctk2p, the CTDK-I C-type cyclin subunit. We show that at steady state under standard exponential growth conditions, Ctk2p comprises two forms, one a phosphorylated form that is very unstable. Our data establish that rapid proteolysis of Ctk2p is mediated by the ubiquitin-proteasome pathway. Strikingly, neither phosphorylation nor degradation of Ctk2p requires its activated kinase.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Yeast strains and growth conditions. The yeast strains used in this study were WCG4a (MATa ura3 leu2-3,112 his3-11,15) and its isogenic pre1-1 pre2-2 derivative WCG4-11/22a, constructed by Richter-Ruoff et al. (48), and MHY501 (MAT his3-200 leu2-3,112 ura3-52 lys2-801 trp1-1) and its isogenic doa4 derivative MHY623, described by Papa and Hochstrasser (45). The ctk strains were derived from W303-1B (MAT ade2-1 can1-100 his3-11,15 leu2-3,112 trp1-1 ura 3-1). Null mutations were obtained by one-step gene replacement (50) by transformation with PCR fragments of the TRP1 gene, using long oligonucleotides containing 5' and 3' sequences of each CTK gene.

Plasmids. CTK1 and CTK3 genes were obtained as BamHI fragments (2,240 and 1,560 bp, respectively) by PCR on genomic DNA. The CTK2 gene was carried into a BglII cosmid fragment (1,970 bp). To verify the disrupted strains, each gene was cloned into a URA3 CEN plasmid. For overexpression experiments, each gene was cloned on a URA3 2µm plasmid. The epitope-tagged CTK2 gene was constructed via several cloning steps. First, a PCR BamHI fragment containing the CTK2 open reading frame was inserted into the BamHI site of plasmid TL38 (LEU2 2µm) (4). The resulting construct, TL38-CTK2, allowed the expression of a Ctk2p protein fused to two influenza virus hemagglutinin (HA) epitope tags at its N terminus, under the control of the PGK promoter. Second, CTK2 promoter sequences were cloned into pFL38 (URA3 CEN) (3) by insertion of a 940-bp BamHI-NcoI/SalI PCR fragment into the BamHI and SalI sites of the vector, yielding pFL38-PrCTK2. Third, the tagged CTK2 open reading frame was cloned under the control of the CTK2 promoter by insertion of the TL38-CTK2 NcoI-XhoI fragment into the NcoI and XhoI sites of pFL38-PrCTK2. The final construct, CTK2-HA (URA3 CEN), allows expression of a tagged Ctk2p under the control of its own promoter. Plasmid YEp96 (TRP1 2µm Ub) (10) contains a synthetic yeast wild-type ubiquitin gene under the control of the copper-inducible CUP1 promoter. YEp105 (TRP1 2µm Myc-Ub) and YEp110 (TRP1 2µm UbK48R) are identical to YEp96, except that they encode a c-Myc-tagged ubiquitin (11) and a mutant ubiquitin with an arginine instead of lysine at amino acid position 48, respectively (21).

Yeast cell extracts and Western immunoblotting. Cells were grown to an optical density at 600 nm (OD₆₀₀) of 0.8 or 3. When indicated, cycloheximide (10 µg/ml; Sigma) was added, and aliquots were frozen after different times of incubation. Cells (10 OD₆₀₀ units) were resuspended in 100 µl of ice-cold trichloroacetic acid (TCA) buffer (20 mM Tris-HCl [pH 8], 50 mM ammonium acetate, 2 mM EDTA, 1 mM phenylmethylsulfonyl fluoride [PMSF]). Cell suspensions were transferred to microcentrifuge tubes containing 100 µl of glass beads (425 to 600 µm in diameter; Sigma) and 100 µl of ice-cold 20% TCA. Cells were disrupted by vigorous vortexing (four times for 1 min each) with 1 min on ice between each vortexing. The beads were washed with 500 µl of an ice-cold 1:1 mixture of 20% TCA and TCA buffer and vortexing twice for 1 min each time. Resulting extracts were centrifuged for 20 min at 4°C at 15,000 rpm, and pellets were resuspended in 100 µl of TCA-Laemmli loading buffer (120 mM Tris base, 3.5% sodium dodecyl sulfate [SDS], 8 mM EDTA, 5% -mercaptoethanol, 1 mM PMSF, 15% glycerol, 0.01% bromophenol blue). Samples were boiled for 10 min and centrifuged at 15,000 rpm for 10 min. Supernatants were collected, and 10-µl aliquots were immediately loaded on an SDS-13% polyacrylamide gel (acrylamide-bisacrylamide, 33.5:0.3) for polyacrylamide gel electrophoresis (PAGE).

ctk2

Phosphatase analyses. Cells (10 OD₆₀₀ units) were broken with 10% TCA as described above. After centrifugation, pellets were resuspended in 100 µl of 50 mM Tris-HCl (pH 7.5)-2% SDS and cleared by centrifugation. Aliquots of 20 µl were incubated with 2 U of alkaline phosphatase (calf intestinal phosphatase; Pharmacia Biotech) in a final volume of 750 µl of 50 mM Tris-HCl (pH 7.5)-1 mM MgCl₂ at 37°C. When indicated, phosphatase inhibitors (100 mM Na₂HPO₄-NaH₂PO₄ [pH 7.5], 10 mM EDTA) were added. Proteins were precipitated for 15 min on ice with 750 µl of cold 50% TCA. After centrifugation, pellets were resuspended in 15 µl of TCA-Laemmli loading buffer with heating at 100°C for 10 min. Samples of 10 µl were loaded on an SDS-13% polyacrylamide gel and Western immunoblotted as described above.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Overexpression of Ctk2p cyclin is toxic. The S. cerevisiae CTDK-I complex is encoded by three genes: CTK1, encoding a CDK subunit; CTK2, encoding a C-type cyclin subunit; and CTK3, encoding a subunit of unknown function. Disruption of any of these genes generates viable cells that display similar growth defects and are unable to grow at low temperatures (56). Cell cycle cyclins expression is tightly regulated at the level of both transcription and protein stability (43). As a consequence, overexpression of cell cycle cyclins usually generates growth defects (9, 60, 68). The CTDK-I complex is implicated not in cell cycle regulation but rather in transcription regulation (26, 31). Similarly to what has been observed for other C-type cyclins implicated in transcription control, CTK2 mRNA levels do not fluctuate during the cell cycle (data not shown). However, because Ctk2p belongs to the cyclin family of proteins, its expression was also expected to be highly regulated. We therefore wanted to know whether its overexpression would generate growth defects. Each protein of the CTDK-I complex was overexpressed by introducing into wild-type cells multicopy plasmids carrying each coding sequence under the control of its cognate promoter. Growth rates were measured for cells grown in minimal medium at 30 and at 15°C (Table 1). Under both conditions, growth rates observed for cells overexpressing either Ctk1p or Ctk3p were identical to that observed for cells carrying a control plasmid, whereas cells overexpressing the Ctk2p cyclin showed significantly slower growth (Table 1). To confirm that overexpression of Ctk2p during exponential growth was toxic for the cells, plasmid loss was quantified. Strains were grown in rich medium for several generations prior to testing for plasmid retention. Whereas similar loss rates were obtained for cells carrying either a plasmid control or cells overexpressing Ctk1p or Ctk3p, cells overexpressing Ctk2p showed a much higher plasmid loss rate (Table 1). Taken together, these results show that overexpressing the C-type cyclin Ctk2p is toxic for the cells. This effect is consistent with a potential tight control of the Ctk2 cyclin C protein expression.

Ctk2p is phosphorylated in vivo. To study Ctk2p expression, its coding sequence was cloned on a single-copy plasmid under the control of the CTK2 promoter sequences. The protein was fused at its N-terminal extremity to influenza virus HA epitope tags. The resulting construct, CTK2-HA, allowed expression of a functional protein because it could restore ctk2 cell growth at the nonpermissive temperature (data not shown). Western blot analyses permitted detection of two specific bands corresponding to the expected size for Ctk2p (p38), the upper band being present at lower quantities (Fig. 1A). In an attempt to identify these two forms, extracts were treated with alkaline phosphatase (Fig. 1B). Treatment of extracts with alkaline phosphatase in the absence, but not in the presence, of phosphatase inhibitors resulted in the loss of the species with lower mobility. This loss was concomitant with an increase in the levels of the higher-mobility species, showing that it was due to serine and/or threonine dephosphorylation. In early exponentially growing cells, at steady state, Ctk2p occurs as two forms, one corresponding to a phosphorylated form (hereafter called Ctk2p-P).

View larger version (32K): [in this window] [in a new window]   FIG. 1.   Ctk2p phosphorylation in vivo. Cells were grown in SD medium to an OD600 of 0.8. (A) Extracts from ctk2 strain transformed with a plasmid control (T) or with the CTK2-HA construct (T+) were analyzed by Western immunoblotting. Arrows indicate bands corresponding to Ctk2p. (B) Extracts from the ctk2 strain transformed with the CTK2-HA construct were incubated for different times (minutes) at 37°C in phosphatase buffer with 2 U of alkaline phosphatase in the absence or presence (+I) of phosphatase inhibitors. In all figures, asterisks mark a nonspecific band which remained stable during all experiments, showing that all lanes were equally loaded.

Ctk2p is unstable. Protein stability is known to play an important role in regulation (19). In yeast, G₁ and mitotic cyclins as well as CDK inhibitors have been shown to be very unstable (23). Cyclin abundance is often rate limiting for CDK activity, and control of cyclin degradation rate is important in regulating cell cycle transitions. Examination of the yeast C-type cyclin Ume3p regulation showed that this cyclin is subjected to rapid destruction (6). To study Ctk2p stability, cycloheximide, an inhibitor of cytoplasmic translation, was added to cultures grown at 30°C in SD medium. Ctk2p levels were monitored by immunodetection. The lower band corresponding to the nonphosphorylated form of the cyclin was relatively unstable (half-life, 60 min; Fig. 2A). Furthermore, the upper band corresponding to the phosphorylated form was highly unstable, as we could not detect it 10 min after cycloheximide addition (Fig. 2A). To get a better insight into Ctk2p-P turnover, its levels were followed just after cycloheximide addition (Fig. 2B). Only 5 min after blocking protein synthesis, we could detect half of the initial levels of Ctk2p-P (half-life, 5 min; Fig. 2B). The same experiments conducted with a Myc-tagged Ctk2p protein generated identical results (data not shown). We conclude that Ctk2p is unstable in exponentially growing cells.

View larger version (46K): [in this window] [in a new window]   FIG. 2.   Ctk2p turnover in early exponential cells. ctk2 cells transformed with the CTK2-HA construct were grown in SD medium to an OD600 of 0.8. Aliquots were taken at different times (minutes) of incubation at 30°C after the addition of cycloheximide. Resulting cellular extracts were analyzed by Western immunoblotting. After the addition of cycloheximide, Ctk2p levels were monitored for 180 min (A) and 5 min (B) to analyze turnover of the nonphosphorylated and phosphorylated species, respectively.

Ctk2p turnover exhibits growth-related regulation. A recent study showed growth-related changes in phosphorylation of the yeast RNA polymerase II CTD (46). Also, Cooper et al. (6) reported that Ume3p turnover is dependent on environmental changes. For these reasons, we examined Ctk2p expression in cells grown under different conditions. Extracts were made from late exponentially growing cells (OD₆₀₀ = 3). Western blot analyses permitted detection of only one band whose migration corresponded to that of the nonphosphorylated form (Fig. 3). Ctk2p stability was determined after cycloheximide addition. In contrast to our previous observations made from cells grown to an OD₆₀₀ of 0.8, Ctk2p levels did not vary for 4 h after inhibition of protein synthesis. This result shows that in late exponentially growing cells, Ctk2p turnover is dramatically reduced, indicating that the regulation of Ctk2p turnover is dependent on growth conditions. Concomitant with this process, we could not detect phosphorylated Ctk2p species, suggesting that either Ctk2p is not phosphorylated or Ctk2p-P is extremely rapidly dephosphorylated.

View larger version (30K): [in this window] [in a new window]   FIG. 3.   Ctk2p turnover in late exponential cells. ctk2 cells transformed with the CTK2-HA construct were grown in SD medium to an OD600 of 3. Aliquots were taken at different times (minutes) of incubation at 30°C after the addition of cycloheximide. Resulting cellular extracts were analyzed by Western immunoblotting. T+, protein extracts from ctk2 cells transformed with the CTK2-HA construct grown to an OD600 of 0.8.

Ctk2p-P degradation is impaired in a mutant defective in proteasome activity. Eukaryotic cells contain two distinct systems for protein degradation: intravacuolar proteolysis (63) and a ubiquitin-mediated proteolysis that involves the proteasome and occurs in the cytoplasm as well as in the nucleus (18). Biochemical and genetic evidence indicates that the ubiquitin-proteasome pathway is involved in the degradation of abnormal proteins and regulatory proteins with naturally short half-lives such as cell cycle cyclins (20). Ctk2p turnover was not affected in the vacuolar protease-deficient pra1 prb1 prc1 cps1 mutant strain (17) (data not shown). To establish whether Ctk2p was a substrate for the proteasome degradation pathway, we examined Ctk2p stability in the yeast pre1 pre2 mutant strain, which is defective in two of the proteasome catalytic subunits (48). The CTK2-HA construct was introduced into pre1 pre2 and wild-type isogenic cells. Cultures were subjected to a shift to the nonpermissive temperature (37°C) prior to addition of cycloheximide to impose the block in proteasome function. In wild-type cells, immunodetection of Ctk2p-P revealed a turnover of a few minutes, similar to what was previously observed (Fig. 4A). In contrast, in pre1 pre2 cells, Ctk2p-P levels remained unchanged 10 min after cycloheximide addition (Fig. 4B). We note that before cycloheximide addition, the Ctk2p-P/Ctk2p ratio was different from that observed previously, indicating that it is dependent on genetic background and/or temperature. In conclusion, Ctk2p-P is dramatically stabilized in a mutant strain that exhibits defects in the activity of the proteasome, showing that its degradation is mediated by the 26S proteasome pathway.

View larger version (28K): [in this window] [in a new window]   FIG. 4.   Ctk2p turnover in cells that have impaired catalytic proteasome subunits. WCG4a (wild type [WT]; A) and isogenic WCG4-11/22a (pre1 pre2; B and C) cells transformed with the CTK2-HA construct were grown in SD medium to an OD600 of 0.8. For panels A and B, cultures were then shifted to the nonpermissive temperature (37°C) for 40 min prior to the addition of cycloheximide, and aliquots were taken at different times (minutes) of incubation at 37°C. (C) Cultures were shifted to the nonpermissive temperature for 1 or 3 h. Resulting cellular extracts were analyzed by Western immunoblotting.

Ctk2p-P degradation is an ubiquitin-mediated process. Although the 26S proteasome degrades an unknown number of proteins that are recognized without undergoing ubiquitination, the ubiquitin system constitutes the major targeting process leading to selective degradation (47). Ubiquitin is covalently attached to the protein substrate through an isopeptide bond in a multistep reaction, and repeated ubiquitination reactions culminate in attachment of a multiubiquitin chain that marks the target protein for rapid degradation by the 26S proteasome (20). Ubiquitin hydrolases act to remove ubiquitin from conjugated forms during either protein degradation or signalling. Cells disrupted for the DOA4 gene encoding a deubiquitinating enzyme are disturbed for normal metabolism of ubiquitin and display a strong inhibition of the turnover of several soluble substrates of the ubiquitin pathway (45). To determine if Ctk2p degradation was mediated by the ubiquitin pathway, we studied Ctk2p turnover in cells disrupted for the DOA4 gene. We compared the rates of Ctk2p turnover in doa4 and isogenic wild-type cells after inhibition of protein synthesis. As previously observed, Ctk2p-P turnover was very fast in wild-type cells, whereas the amounts of immunodetected Ctk2p-P in doa4 cells decreased only slightly after 15 min (Fig. 5A). Similar to what was observed in a proteasome mutant strain, Ctk2p-P degradation was strongly affected in doa4 mutant cells. Several studies have suggested that the amount of intracellular ubiquitin available for ubiquitination is limiting in doa4 cells (15, 45, 54). To find out whether an increase in ubiquitin levels could restore Ctk2p instability in the doa4 mutant strain, wild-type and doa4 cells were transformed with the multicopy plasmid YEp96, encoding a synthetic ubiquitin gene under the control of a CUP1-inducible promoter (10). CuSO₄ was added for 5 h to induce the CUP1 promoter, and Ctk2p levels were monitored by immunodetection after cycloheximide addition. Overexpression of wild-type ubiquitin did not affect Ctk2p-P turnover in wild-type cells (data not shown). In contrast, overexpression of ubiquitin rescued Ctk2p-P turnover in doa4 cells (half-life, 5 to 10 min; Fig. 5B). In summary, we observed a significant stabilization of Ctk2p-P in doa4 cells. This effect was partially reversed by overproduction of wild-type ubiquitin, suggesting that an ubiquitin-mediated process is required for Ctk2p-P rapid degradation.

View larger version (35K): [in this window] [in a new window]   FIG. 5.   Ctk2p degradation is a ubiquitin-dependent process. Cells were grown in SD medium to an OD600 of 0.8, and aliquots were taken at different times (minutes) of incubation at 30°C after the addition of cycloheximide. Resulting cellular extracts were analyzed by Western immunoblotting. (A) MHY501 (wild type [WT]) and isogenic MHY623 (doa4) cells transformed with the CTK2-HA construct. (B) doa4 cells cotransformed with the CTK2-HA and YEp96 (wild-type ubiquitin [wt Ub]) plasmids. (C) MHY501 (wild type) cells cotransformed with the CTK2-HA and YEp110 (UbK48R) plasmids. In the right portions (+ Induction) of panels B and C, cells were grown for 5 h with CuSO4 before they reached an OD600 of 0.8 in order to induce ubiquitin expression from the CUP1 promoter.

doa4

doa4

View larger version (46K): [in this window] [in a new window]   FIG. 6.   Ctk2p ubiquitin conjugates. W303-1B (wild type) cells cotransformed with plasmid YEp105 (Myc-tagged ubiquitin [Myc-Ub]) and either a control plasmid () or the CTK2-HA construct were grown in SD medium to an OD600 of 0.8 or 3 as indicated. CuSO4 was (+) or was not () added overnight to the cultures in order to induce expression of the Myc-tagged ubiquitin. After immunoprecipitation with HA polyclonal antibodies, proteins were analyzed by Western immunoblotting with monoclonal Myc (upper panel) and monoclonal HA (lower panel) antibodies successively. Arrows and asterisks indicate bands corresponding to Ctk2p and nonspecific products, respectively.

Ctk2p is phosphorylated in cells lacking the Ctk1p kinase. Cell cycle cyclins have been shown to be rapidly degraded via the ubiquitin-proteasome pathway, and in several cases, mutagenesis analyses revealed that phosphorylation by their associated kinase provides a signal that promotes this process (28, 68). The fact that degradation of a cyclin is dependent on its cognate CDK subunit renders the cyclin-activated CDK activity self-limiting. To determine whether Ctk2p phosphorylation was dependent on its cognate kinase subunit, CTK2-HA construct was introduced into cells disrupted for the CTK1 gene. Western blots analyses allowed detection of two bands corresponding to Ctk2p (Fig. 7), showing that the cyclin Ctk2p was phosphorylated in the absence of its activated kinase. Moreover, after cycloheximide addition, we observed a similar turnover for the phosphorylated form in ctk1 cells compared to wild-type cells (half-life, 5 min; Fig. 7 and data not shown). We note that Ctk2p abundance was lower in ctk1 mutant cells than in wild-type cells, consistent with Northern blots analyses showing that CTK2 mRNA steady-state levels were substantially diminished in ctk1 cells (data not shown). Also, the Ctk2p-P/Ctk2p ratio was slightly lower in ctk1 cells than in wild-type cells, this effect being correlated with a significant stabilization of the unphosphorylated form. If Ctk2p phosphorylation is not as efficient in ctk1 cells as in wild-type cells, as a consequence one would expect to observe its stabilization. To obtain a better insight into the regulation of Ctk2p turnover in ctk1 cells, we analyzed Ctk2p expression in ctk1 cells grown to an OD of 3. As previously observed in wild-type cells (Fig. 3), Ctk2p was composed of only one band corresponding to the unphosphorylated form (data not shown). In conclusion, if there is a slight difference in Ctk2p turnover in ctk1 cells, it is probably nonspecifically affected due to the fact that Ctk2p is not an active protein, as it cannot be part of the CTDK-I complex.

View larger version (38K): [in this window] [in a new window]   FIG. 7.   Ctk2p phosphorylation in ctk1 cells. ctk1 cells transformed with the CTK2-HA construct were grown in SD medium to an OD600 of 0.8. Aliquots were taken at different times (minutes) of incubation at 30°C after the addition of cycloheximide. Resulting cellular extracts were analyzed by Western immunoblotting. As a control (T+), protein extracts from ctk2 cells transformed with the CTK2-HA construct grown to an OD600 of 0.8 were loaded on the gel.

ctk1

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

The C-type cyclin Ctk2p is phosphorylated in vivo. We have studied the expression of the yeast C-type cyclin Ctk2p, a cyclin subunit of the CTDK-I complex that is implicated in phosphorylation of the RNA polymerase II CTD. We show that steady-state levels of Ctk2p in pseudo-wild-type exponential-phase cells (a functional tagged version of the cyclin was expressed from its cognate promoter carried by a single-copy plasmid introduced into ctk2 cells) are composed of two forms, one a phosphorylated form. This is the first description of a C-type cyclin phosphorylation. Examination of Ctk2p protein sequence did not reveal the presence of a strong PEST-rich motif, and as yet no phosphorylated residues have been identified. One difficulty in studying cell cycle cyclins at the protein levels is that yeast cells contain very little of these proteins. In contrast, phosphorylated as well as nonphosphorylated species of Ctk2p are relatively abundant during exponential growth. This striking feature might reflect a role for Ctk2p in regulating transcription rather than cell cycle progression. Indeed, cell cycle CDKs are known to interact sequentially with several distinct cyclins whose abundance fluctuates during the cell cycle (43). Yeast CDKs activated by C-type cyclins seem to be an exception from this principle, as only one cyclin has been characterized per kinase subunit, indicating clearly that different features govern regulation of CDKs that are implicated in transcription control.

Ctk2p degradation is mediated by the ubiquitin-proteasome pathway. We have blocked cytoplasmic translation with cycloheximide to study Ctk2p stability. We show that under these conditions, Ctk2p is a moderately unstable protein (half-life, 60 min) whereas its phosphorylated form is extremely unstable (half-life, 5 min). Because C-type cyclin expression may vary upon diverse stress conditions, pulse-chase experiments would be required to determine whether Ctk2p turnover is affected by cycloheximide.

doa4

Control of Ctk2p turnover. Patturajan et al. (46) reported recently that the pattern of CTD phosphorylation in yeast varies in response to growth conditions and environmental stress. Among the three C-type cyclins identified in yeast, Ume3p and Ctk2p are associated with nonessential CTD kinases that are implicated in transcription regulation. Ume3p is rapidly destroyed when cells enter the meiotic pathway or are exposed to heat shock (6). Ctk2p is expected to be stabilized whenever CTDK-I kinase activity is required. In this report, we show that Ctk2p is very stable in late-exponential-phase cells, demonstrating that this regulatory protein is not constitutively short-lived.