Potential conflict of interest: Nothing to report.
Ubiquitin-conjugating enzyme 9 (Ubc9) is required for sumoylation and is overexpressed in several malignancies, but its expression in hepatocellular carcinoma (HCC) is unknown. Hepatic S-adenosyl methionine (SAMe) levels decrease in methionine adenosyltransferase 1A (Mat1a) knockout (KO) mice, which develop HCC, and in ethanol-fed mice. We examined the regulation of Ubc9 by SAMe in murine liver and human HCC, breast, and colon carcinoma cell lines and specimens. Real-time polymerase chain reaction and western blotting measured gene and protein expression, respectively. Immunoprecipitation followed by western blotting examined protein-protein interactions. Ubc9 expression increased in HCC and when hepatic SAMe levels decreased. SAMe treatment in Mat1a KO mice reduced Ubc9 protein, but not messenger RNA (mRNA) levels, and lowered sumoylation. Similarly, treatment of liver cancer cell lines HepG2 and Huh7, colon cancer cell line RKO, and breast cancer cell line MCF-7 with SAMe or its metabolite 5′-methylthioadenosine (MTA) reduced only Ubc9 protein level. Ubc9 posttranslational regulation is unknown. Ubc9 sequence predicted a possible phosphorylation site by cell division cycle 2 (Cdc2), which directly phosphorylated recombinant Ubc9. Mat1a KO mice had higher phosphorylated (phospho)-Ubc9 levels, which normalized after SAMe treatment. SAMe and MTA treatment lowered Cdc2 mRNA and protein levels, as well as phospho-Ubc9 and protein sumoylation in liver, colon, and breast cancer cells. Serine 71 of Ubc9 was required for phosphorylation, interaction with Cdc2, and protein stability. Cdc2, Ubc9, and phospho-Ubc9 levels increased in human liver, breast, and colon cancers. Conclusion: Cdc2 expression is increased and Ubc9 is hyperphosphorylated in several cancers, and this represents a novel mechanism to maintain high Ubc9 protein expression that can be inhibited by SAMe and MTA. (HEPATOLOGY 2012;56:982–993)
Posttranslational modification regulates the activity, localization, intracellular levels, and interaction of proteins with other molecules.1 Sumoylation is small ubiquitin-related modifier (SUMO) conjugation that is similar to ubiquitination in the conjugation process and attachment to target proteins. However, unlike ubiquitination that normally targets proteins for degradation through proteasome pathways, sumoylation regulates protein stability, protein-protein interactions, transcriptional activity, and trafficking.2
Sumoylation is a multistep process catalyzed by E1, E2, and E3 enzymes that include activating SUMO, conjugation ending with the formation of an isopeptide bond between the C-terminal Gly residue of SUMO and the ε-amino group of a Lys residue in the acceptor protein.2 Ubiquitin-conjugating enzyme 9 (Ubc9) is the only well-characterized E2 enzyme in the sumoylation cycle that transfers the activated SUMO to the target protein.3
Ubc9 and SUMO are highly expressed in human premalignant conditions in response to low-grade, long-term oxidative stress, suggesting that up-regulation of sumoylation may be an adaptive response to oxidative stress.4, 5 Ubc9 may be fundamental for tumorigenesis and tumor progression by minimizing the acute cellular stress response associated with the accumulating DNA damage of tumor progression.5 Consistently, Ubc9 is overexpressed in several malignancies, such as lung adenocarcinoma, colorectal cancer, breast adenocarcinoma, and melanoma.6-8 Ubc9 expression in hepatocellular carcinoma (HCC) has not been reported.
Chronic hepatic S-adenosyl methionine (SAMe) deficiency generates oxidative stress9, 10 and predisposes to injury and malignant transformation.11 SAMe, generated in the first reaction of methionine metabolism catalyzed by methionine adenosyltransferase (MAT), is the principal biological methyl donor and a precursor for glutathione and polyamines.11 In the biosynthesis of polyamines, 5′-methylthioadenosine (MTA) is generated as an end product.12 SAMe is also degraded spontaneously to MTA intra- and extracellularly.13 The catalytic subunit of MAT is the product of two different genes: MAT1A, which is expressed mainly in the adult liver, and MAT2A, which is widely distributed, expressed in the fetal liver, and replaces MAT1A in HCC.11 Consequences of hepatic SAMe deficiency as illustrated by the Mat1a knockout (KO) and intragastric ethanol infusion mouse models include increased susceptibility to oxidative liver injury and HCC.9, 10, 14
Here, we report that Ubc9 expression and hence sumoylation are increased when hepatic SAMe levels decrease. Our findings reveal for the first time that Ubc9 stability is regulated by SAMe and MTA through a change in Ubc9 phosphorylation. In addition, we identified Ubc9 as a substrate of cell division cycle 2 (Cdc2), which is overexpressed in many cancers and when SAMe levels decrease. These changes occur in many types of cancers, including HCC, colon, and breast. Our findings have important implications in the regulation of Ubc9 and sumoylation.
SAMe, in the stable form of disulfate p-toluene sulfonate dried powder, was generously provided by Gnosis SRL (Cairate, Italy). MTA was obtained from Sigma-Aldrich (St. Louis, MO), roscovitine was obtained from Calbiochem (San Diego, CA), and phosphatase inhibitor cocktail was obtained from Thermo Scientific (Rockford, IL). [γ-32P]ATP (3,000 Ci/mmol) was obtained from Perkin Elmer (Waltham, MA). Recombinant Cdc2/cyclin B complex was obtained from New England Biolabs (Ipswich, MA), and Ubc9 recombinant protein was obtained from Prospec (Rehovot, Israel).
Cell Culture and Treatments.
HepG2, Huh7, and RKO cells were obtained from the Cell Culture Core of the USC Research Center for Liver Diseases. MCF-7 cells were purchased from American Type Cell Collection (Manassas, VA). All cell lines were grown according to instructions provided by American Type Cell Collection. Prior to treatment with SAMe or MTA, medium was changed to 1% fetal bovine serum overnight. Cells were then treated with SAMe (2 mmol/L) or MTA (1 mmol/L) for up to 24 hours. Because of the instability of SAMe, medium was changed every 6 hours for all conditions. In other experiments, RKO cells were treated with a phosphatase inhibitor mixture (1:10,000 to 104 mM AEBSF-[4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride], 80 μM aprotinin, 4 mM bestatin hydrochloride, 1.4 mM E-64-[N-(trans-epoxysuccinyl)-L-leucine 4-guanidinobutylamide], 2 mM leupeptin hemisulfate salt, 1.5 mM pepstatin A) for 24 hours.
Mat1a KO Mice and Treatment.
Male Mat1a KO and wild-type (WT) littermates have been described.14 Mice were given 100 mg/kg/day SAMe dissolved in water or equal volume of water by oral gavage and were sacrificed after 7 days. Liver tissues were removed, snap-frozen in liquid nitrogen, and stored at −80°C until analysis. Animals were treated humanely, and all procedures were in compliance with our institutional guidelines for the use of laboratory animals.
Intragastric Ethanol Infusion.
The intragastric ethanol infusion model has been described.15 Male C57/B6 mice received a high-fat diet (35% calories as corn oil) along with an increasing dose of ethanol (22.7-35 g/kg/day for mice) or isocaloric dextrose solutions for 4 weeks. Iron dextran (25 or 75 mg/kg) was injected subcutaneously 2 weeks before 4 weeks of alcohol feeding. The animals were treated in accordance with our institutional guidelines for the use of laboratory animals.
Twelve each of colon, HCC, and breast adenocarcinoma and corresponding surrounding nontumorous tissues were used. Colon tissues were obtained by P. Giordano (Whipps Cross University Hospital, London, UK). Liver and breast tissues were obtained by R. M. Pascale (University of Sassari, Italy). These tissues were immediately frozen in liquid nitrogen for subsequent RNA and protein extraction.
Written informed consent was obtained from each patient. The study protocol conformed to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in a prior approval by the Keck School of Medicine's human research review committee.
RNA Extraction and Real-Time Polymerase Chain Reaction Analysis.
Total RNA isolated from cells and livers as described16 was subjected to reverse transcription by using M-MLV Reverse Transcriptase (Invitrogen, Carlsbad, CA). One microliter of reverse transcription product was subjected to quantitative real-time polymerase chain reaction (PCR) analysis. The primers and TaqMan probes for Ubc9, Cdc2, PP1, and Universal PCR Master Mix were purchased from ABI (Foster City, CA). 18SrRNA was used as a housekeeping gene as described.17 The delta Ct (ΔCt) obtained was used to find the relative expression of genes according to the following formula: relative expression = 2−ΔΔCt, where ΔΔCt = ΔCt of respective genes in experimental groups − ΔCt of the same genes in control group.
The predesigned small interfering RNA (siRNA) targeting human Cdc2 (sense sequence: CCUAGUACUGCAAUUCGGGAAAUUU) (Invitrogen, Carlsbad, CA), PP1 (sense sequence: CCGCAATTCCGCCAAAGCCAA) (Qiagen, Valencia, CA), and negative control siRNA (Ambion, Austin, TX) were purchased. HepG2, RKO, and MCF-7 cells were cultured in 100-mm2 dishes (1 × 106 cells/dish) and transfected using RNAiMax (18 μL/dish) from Invitrogen (Carlsbad, CA) with Cdc2 siRNA (30 nM) or negative control siRNA for 48 hours for messenger RNA (mRNA) or protein expression, following the manufacturer's instructions.
Overexpression of WT and Mutant Ubc9.
Ubc9 overexpression vector (Ubc9-pCMV4-HA) and negative control empty vector (pCMV4-HA) were purchased from Addgene (Cambridge, MA). Mutation of Ser70 or Ser71 of Ubc9 to phenylalanine was performed using the Quick Change II Site-Directed Mutagenesis Kit (Stratagene, La Jolla, CA) with pCMV4 as the template. RKO cells were cultured in 100-mm2 dishes (1 × 106 cells/dish) and transfected using 60 μL of Superfect from Qiagen (Valencia, CA) and 5 μg of target plasmid per dish. After 4 hours, the transfection medium was changed to normal medium. Protein expression and interaction were examined 48 hours later.
Western Blots and Co-immunoprecipitation.
Protein extracts from cells and tissue samples were prepared as described18 and immunoprecipitated by specific Ubc9 antibody (Santa Cruz Biotechnology, Santa Cruz, CA) and processes as reported.19 Immunoprecipitated proteins were subjected to western blotting following standard protocols (Amersham BioSciences, Piscataway, NJ), and the membranes were probed with the anti–protein phosphatase 1 (PP1), anti-Cdc2 (Santa Cruz Biotechnology, Santa Cruz, CA), anti–SUMO-1 that detects recombinant SUMO-1 and endogenous levels of sumoylated proteins (e.g., SUMO-1 RanGAP) (Cell Signaling, Danvers, MA), and anti-phosphorylated (phospho) protein (Pan)[pS/pT/pY] (Invitrogen, Carlsbad, CA) antibodies. Blots were developed using enhanced chemoluminescence.
In Vitro Assay of Kinase Activity.
Recombinant Ubc9 (2 μg) was phosphorylated by the purified recombinant Cdc2/cyclin B complex (10 ng) in a final volume of 30 μL containing 50 mM Tris-HCl (pH 7.5), 10 mM MgCl2, 1 mM ethylene glycol tetraacetic acid, 1 mM dithiothreitol, 100 μM ATP, and 10 μCi [γ-32P]ATP. The reaction mixture was incubated for the indicated times at 30°C, after which proteins were separated by sodium dodecyl sulfate–polyacrylamide gel electrophoresis on a 12% gel. The radioactivity associated with protein bands was quantified by Quantity One (Biorad, Hercules, CA).
Protein Stability Assay and Half-Life Determination.
Cycloheximide (5 μg/mL) was added to RKO or Huh7 cells 48 hours after transfection with 2 μg of WT Ubc9-pCMV4 or Ubc9-F71 mutant plasmids per well. Protein levels were determined at indicated time points by western blotting as described above using the anti-HA antibody. The relative amount of Ubc9-HA protein was evaluated by densitometry and normalized to actin. Protein half-life was determined for each experiment using linear regression analysis.
Data are expressed as the mean ± SEM. Statistical analysis was performed using analysis of variance and Fisher's exact test. For mRNA and protein levels, ratios of genes and proteins to respective housekeeping densitometric values were compared. Significance was defined as P < 0.05.
Ubc9 Is Up-regulated in Human HCC.
Ubc9 is overexpressed in several cancers,6-8, 20 but its expression in HCC is unknown. We found Ubc9 mRNA levels increased by 60% while Ubc9 protein levels increased by 140% in HCC compared with surrounding nontumorous tissue (Fig. 1A,B).
Ubc9 Expression Is Up-regulated in Mat1a KO and Ethanol-Fed Mice.
Mat1a KO and ethanol-fed mice exhibited increased oxidative stress, which increased Ubc9 expression and sumoylation.5, 9, 21 Figure 1C,D shows that mRNA and protein levels of Ubc9 increased by 50% and 100%, respectively, in livers of ethanol-fed mice compared with control mice. Similarly, in Mat1a KO mouse livers, Ubc9 mRNA and protein levels increased by 44% and 97%, respectively (Fig. 2A,B). Protein sumoylation increased by 500% in KO mouse livers (Fig. 2C). Because hepatic SAMe levels were reduced in both Mat1a KO and ethanol-fed mice, we examined the effect of SAMe treatment in Mat1a KO mice. SAMe treatment for 1 week, which normalized hepatic SAMe levels in Mat1a KO mice,22 had no effect on Ubc9 mRNA (Fig. 2A), but nearly normalized Ubc9 protein levels (Fig. 2B) and protein sumoylation (Fig. 2C).
Effects of SAMe and MTA on Expression of Ubc9 in HepG2, Huh7, RKO, and MCF-7 Cells.
We next examined the effects of SAMe and its metabolite MTA on Ubc9 expression in liver, colon, and breast cancer cell lines as Ubc9 is overexpressed in colon and breast cancers.8, 20 We included MTA because MTA recapitulates many of the effects of SAMe.13, 17, 23 Consistent with the effect of SAMe in Mat1a KO livers, SAMe and MTA treatment for 24 hours had no effect on Ubc9 mRNA levels in HepG2, Huh7, RKO, and MCF-7 cells (Fig. 3A), but lowered Ubc9 protein levels by about 30%-40% in all of these cells (Fig. 3B). Treatment with SAMe or MTA for 12 hours had no effect on Ubc9 mRNA levels, and the reduction in Ubc9 protein levels was much less (data not shown).
SAMe and MTA Treatment Alter Ubc9′s State of Phosphorylation and Sumoylation.
Phosphorylation can alter protein stability.24 SAMe and MTA inhibited protein phosphorylation in HepG2 cells,23 which prompted us to examine whether they affect Ubc9 phosphorylation. Total protein phosphorylation was examined by western blotting using anti-phospho antibody, while phospho-Ubc9 was determined by first immunoprecipitating total Ubc9, followed by western blotting with anti-phospho antibody. SAMe and MTA treatment resulted in decreased levels of total phosphoproteins and phospho-Ubc9 in all cell lines (Fig. 4A). Total Ubc9 levels decreased in parallel to phospho-Ubc9 levels. In addition, SAMe and MTA suppressed the level of sumoylated RanGAP1 (Fig. 4A), a major SUMO substrate.25 To confirm that the phosphorylation of Ubc9 influences protein stability, we examined the effect of phosphatase inhibitors on Ubc9 protein expression in RKO cells. Figure 4B shows that total Ubc9 and phospho-Ubc9 levels increased after treatment with phosphatase inhibitors, which is consistent with the notion that Ubc9 phosphorylation enhances its stability.
Phosphorylation of Ubc9 by Cdc2/CyclinB Complex In Vitro Assay.
Using DISPHOS 1.3 (Disorder-Enhanced Phosphorylation Sites Predictor), we identified two potential phosphorylated sites at serine 70 and serine 71. We searched for potential protein kinases that may target these sites using the KinasePhos, PostMod, MotifScan, and Phosphonet analysis tools. These four prediction programs all identified several potential protein kinases (Fig. 4C) such as Cdc2 and CDK5. Cdc2 shows a good match to the matrix with a similarity score of 0.8. Matrix scores lower than 0.8 were rejected. To test the possibility that Cdc2 can phosphorylate Ubc9, we performed in vitro kinase assays using highly purified Ubc9 recombinant protein and Cdc2-cyclin B complex in combination with roscovitine, a potent inhibitor of kinase activity. Figure 5A shows that Cdc2 is able to phosphorylate Ubc9 in vitro, and this can be inhibited by roscovitine.
Effect of SAMe and MTA on Cdc2 Expression In Vitro and In Vivo.
Cdc2 overexpression occurs at high frequency in several types of cancer.26 Because the above finding suggests Cdc2 may be involved in the phosphorylation of Ubc9, we next examine the effect of SAMe and MTA on Cdc2 expression. Both SAMe and MTA treatment resulted in a decrease of Cdc2 mRNA and protein levels after 24 hours in RKO cells by 50% (Fig. 5B). To determine whether SAMe and MTA lower Ubc9 protein levels by inhibiting Cdc2 expression, we used Cdc2 siRNA in combination with SAMe (2 mM) and MTA (1 mM) treatment in RKO cells. Knockdown of Cdc2 resulted in a 55% reduction in Ubc9 protein level (Fig. 5C). SAMe and MTA have similar effects on Ubc9 protein level as Cdc2 knockdown, but combining SAMe or MTA with Cdc2 knockdown did not further reduce Ubc9 protein level (Fig. 5C). To verify the relevance of Cdc2 on Ubc9 phosphorylation under in vivo conditions, we examined Mat1a KO livers. Figure 5D shows increased protein levels of total Ubc9, phospho-Ubc9, and Cdc2 that is associated with Ubc9 in Mat1a KO mouse livers, and these were nearly corrected by SAMe treatment. These results also demonstrate interaction of Cdc2 with Ubc9 in vivo that can be modulated by SAMe treatment.
Phosphorylation of Ubc9 in Human Cancer Specimens.
Phosphorylation status of Ubc9 and interaction of Ubc9 with Cdc2 in human cancer specimens have not been reported; we next investigated this in 18 HCC, 12 colorectal cancer, and 12 breast cancer and corresponding surrounding nontumorous tissues by co-immunoprecipitation (co-IP) analysis. Figure 6 shows that the levels of total Ubc9, phospho-Ubc9, Cdc2, and Cdc2 that is associated with Ubc9 are increased in all of these cancers compared with the nontransformed tissues. These results suggest that Cdc2-mediated phosphorylation of Ubc9 may contribute to higher Ubc9 protein level in these cancers.
Serine 71 of Ubc9 Is Critical for Interaction With Cdc2, Phosphorylation of Ubc9, and Ubc9 Protein Stability in RKO Cells.
Finally, to examine whether serine 70 and serine 71 are critical sites of phosphorylation by Cdc2 in native Ubc9 protein and protein stability, we examined whether mutation of S70 and S71 (to F70 and F71) affected phosphorylation of Ubc9 in RKO cells. For this purpose, we created mutations in the overexpression vector hUbc9 HA-tagged at S70 and S71 and examined total Ubc9 protein and phospho-Ubc9 levels and Cdc2 interaction using co-IP analysis. Fig. 7A shows that mutation at S71 (but not S70) significantly reduced interaction with Cdc2, phospho-Ubc9, and total Ubc9 levels. Mutation at S71 resulted in a less stable Ubc9 as demonstrated by measurement of protein half-life, which decreased from 5.8 ± 0.5 hours in WT to 3.8 ± 0.2 in mutant in RKO cells. Similarly, mutation at S71 also lowered Ubc9 half-life from 8.7 ± 1.8 hours to 3.5 ± 0.5 hours in Huh7 cells (results are expressed as the mean ± SEM from three independent experiments for each cell type; P < 0.05) (Fig. 7B,C).
Ubc9 is overexpressed in several malignancies.8, 20 Suppression of Ubc9 function inhibits tumor growth in a breast cancer animal model,20 suggesting that Ubc9 plays a role in tumorigenesis. This is likely due to the fact that Ubc9 is an essential enzyme for sumoylation, and deregulation of Ubc9 could lead to alterations of sumoylation pathways, ultimately impacting cell growth and cancer development.
Ubc9 expression and sumoylation of a broad range of proteins is induced by oxidative stress.4 Oxidative stress is a key component in the induction of HCC.27 However, Ubc9 expression in HCC has not been reported. We found that Ubc9 expression is also increased in HCC (Fig. 1A), but interestingly the protein level is elevated to a higher extent than the mRNA level, suggesting Ubc9 is posttranslationally regulated. Despite the importance of Ubc9 in sumoylation and tumorigenesis, factors that control its regulation remain largely unknown and in particular, posttranslational regulation of Ubc9 has not been reported to our knowledge.
Two other models of increased oxidative stress and predisposition to malignant degeneration are the Mat1a KO mouse model and the ethanol infusion (EI) model of alcoholic liver disease (ALD). The EI model of ALD has been used to study various aspects to ALD pathogenesis.28 However, the effect of EI on Ubc9 expression and hence sumoylation are unknown. We found that hepatic Ubc9 expression is higher at both the mRNA and protein levels in EI mice, and the protein level is increased to a higher degree than the mRNA level (Fig. 1B).
Similar to HCC and ethanol-fed mice, Ubc9 expression is increased in Mat1a KO livers, with the protein level increased to a higher degree than the mRNA level. We previously demonstrated that exogenous SAMe treatment normalized hepatic SAMe levels in Mat1a KO mice,22 which prompted us to examine the effect of SAMe treatment in Mat1a KO mice on Ubc9 expression. Interestingly, SAMe treatment normalized the Ubc9 protein level but had no influence on its mRNA level, suggesting that SAMe destabilized Ubc9 protein. This is an intriguing finding because we had previously shown that SAMe can stabilize dual specificity of mitogen-activated protein kinase phosphatase protein by inhibiting proteasomal activity.22 Thus, the effect of SAMe on Ubc9 seems to contradict this previous finding. This led us to explore mechanisms that might regulate Ubc9 protein stability besides proteasomal activity. Consistent with reduced Ubc9 expression, SAMe treatment in Mat1a KO mice reduced protein sumoylation in the livers (Fig. 2).
We next used cancer cell lines to further investigate the molecular mechanism of SAMe's effect on Ubc9 protein stability. We chose two liver cancer cell lines (HepG2 and Huh7), one colon cancer cell line (RKO), and one breast cancer cell line (MCF-7) because Ubc9 is overexpressed in breast and colon cancers.8, 20 We included MTA in our studies because SAMe is converted to MTA spontaneously at a significant rate13 and many of SAMe's actions may actually be due to MTA.17, 23, 29 SAMe and MTA down-regulated Ubc9 protein levels, without any change in mRNA levels, and protein sumoylation in all cell lines (Figs. 3 and 4A).
We previously demonstrated that SAMe and MTA treatment in HepG2 cells led to increased expression of PP1.23 Protein phosphorylation can either enhance or inhibit protein stability.24, 30 Treatment of Huh7, RKO, and MCF-7 cells with SAMe or MTA lowered overall protein phosphorylation, consistent with our previous results (Fig. 4A). We examined whether the effect of SAMe and MTA occurs through the enhancement of PP1 expression by knocking down PP1 prior to SAMe or MTA treatment. However, this had no effect on SAMe and MTA-mediated down-regulation of Ubc9 protein level (data not shown) so that the mechanism is not via PP1. Ubc9 contains multiple potential phosphorylation sites, but it has not been reported to be phosphorylated. Interestingly, we found that Ubc9 is phosphorylated at baseline and SAMe and MTA treatment lowered Ubc9 phosphorylation in parallel to its total protein level. The finding that inhibiting phosphatases raised total Ubc9 and phospho-Ubc9 levels further supports the notion that Ubc9 phosphorylation stabilizes Ubc9 protein.
Protein phosphorylation predominantly occurs in regions of intrinsic disorder.31 Accordingly, we identified two potential phosphorylated sites at serine 70 and serine 71 in Ubc9 protein sequence. This region contains the -P-X3-P-X2-P-P- motif that is conserved among all members of the Ubc protein family. Mutations occurring in this motif interfered with the in vivo activity of Ubc9 at high temperature and caused a reduction in the abundance of the mutated proteins in yeast.32 In this region, we identified Cdc2 as a potential kinase to phosphorylate the S70-S71 motif. Interaction of Ubc9 with Cdc2 agrees with the matrix similarity score of 0.8, which suggests a high probability that Ubc9 is a Cdc2 substrate. Our in vitro kinase findings verified this and showed that Cdc2 phosphorylated Ubc9 recombinant protein and that roscovitine, an inhibitor of Cdc2, was able to significantly reduce Cdc2-mediated phosphorylation (Fig. 5A). Cdc2 is implicated in the genesis and/or progression of breast cancers26 and is overexpressed in the majority of diffuse large B cell lymphoma specimens.33 To investigate whether SAMe and MTA's effect on Ubc9 protein may involve Cdc2, we examined the effect of SAMe and MTA on Cdc2 expression. Surprisingly, we found that Cdc2 expression decreased at both mRNA and protein levels after SAMe and MTA treatment. Furthermore, silencing Cdc2 reduced Ubc9 protein levels by a similar magnitude as SAMe and MTA treatments. Combining Cdc2 knockdown with either SAMe or MTA did not reduce Ubc9 protein level or phospho-Ubc9 further, suggesting that the inhibitory effect of SAMe and MTA on Ubc9 protein level is mediated largely via down-regulation of Cdc2 expression (Fig. 5C). Physical interaction of Ubc9 and Cdc2 was demonstrated in Mat1a KO livers, and this was reduced by SAMe treatment (Fig. 5D). Taken together, our results support the notion that Cdc2 can interact with Ubc9 to phosphorylate it and increase its protein stability.
Because Ubc9 phosphorylation and interaction with Cdc2 in human cancers have not been reported, we next examined this in HCC, colorectal, and breast cancer specimens. We found that the levels of total Ubc9, phospho-Ubc9, Cdc2, and Cdc2 that is associated with Ubc9 are all increased in these cancers. The degree of increase in total Ubc9 exceeds that of phospho-Ubc9 in cancer specimens, suggesting that other factors also contribute to a higher total Ubc9 protein expression. Consistent with this, Ubc9 has been shown to be a target of miR-30e, which is down-regulated in several tumors.6 Taken together, it is likely that the higher level of Cdc2 that is associated with Ubc9 resulted in higher phospho-Ubc9 in these cancer specimens, and this along with other contributing mechanisms resulted in higher Ubc9 expression.
To determine whether Cdc2 interaction and phosphorylation of Ubc9 occurs at the S70-S71 motif, we mutated these amino acids. Mutating S71 led to a reduction of Cdc2 binding to Ubc9, Ubc9 phosphorylation, and total Ubc9 protein level. Furthermore, mutating S71 resulted in a less stable Ubc9, as demonstrated by protein stability assay. These results demonstrate that Cdc2 plays an important role as a positive regulator of Ubc9 expression in human carcinogenesis. They also demonstrate that posttranslational regulation of Ubc9 by Cdc2 contributes to the higher Ubc9 protein than mRNA levels in HCC.
There are multiple SUMO proteins (SUMO-1, -2, -3, and -4), and because Ubc9 (SUMO E2) is required for sumoylation, we focused on Ubc9. This work is the first to demonstrate that sumoylation is increased when cellular SAMe levels decrease and is decreased by exogenous treatment with SAMe or MTA. Interestingly, SUMO E1 enzyme is also elevated in HCC and correlates with a lower survival rate.34 Whether SAMe and MTA also regulate SUMO proteins and SUMO E1 and E3 enzymes remains to be examined.
In conclusion, we have revealed a novel mechanism of Ubc9 posttranslational regulation by Cdc2. We have also uncovered a novel mechanism of SAMe's action. Exogenous treatment of liver, colon, and breast cancer cells with SAMe and its metabolite MTA lowered Cdc2 expression, Ubc9 phosphorylation, and total Ubc9 protein level. Figure 8 summarizes key findings from this work. SAMe has been shown to be chemopreventive in several animal models of HCC.35, 36 This may represent a new mechanism of that action. Given the importance of Ubc9 in sumoylation, our findings have important implications in biology and pathology. They also support SAMe and MTA as chemopreventive agents.