CDK1 substitutes for mTOR kinase to activate mitotic cap-dependent protein translation

Significance Cancer cell proliferation is highly dependent on cap-dependent protein synthesis, which is generally assumed to be inhibited during mitosis. Using a viral oncoprotein that enforces mitosis, we show that CDK1 substitutes for mTOR interphase functions to phosphorylate eukaryotic initiation factor 4E-binding protein (4E-BP1) to a mitosis-specific δ isoform. Flow cytometric assays reveal that mitotic cells have high levels of inactivated 4E-BP1 and do not generally show specific loss of cap-dependent translation compared with interphase cells. This appears to be due to cyclin-dependent kinase 1 (CDK1) activity during mitosis. Mitotic cells typically represent less than 1% of all cells in bulk culture, and mitosis-arresting drugs, such as nocodazole, can directly inhibit mitotic protein translation, potentially explaining differences between our findings and previous studies showing reduced cap-dependent translation during mitosis.

Mitosis is commonly thought to be associated with reduced capdependent protein translation. Here we show an alternative control mechanism for maintaining cap-dependent translation during mitosis revealed by a viral oncoprotein, Merkel cell polyomavirus small T (MCV sT). We find MCV sT to be a promiscuous E3 ligase inhibitor targeting the anaphase-promoting complex, which increases cell mitogenesis. MCV sT binds through its Large T stabilization domain region to cell division cycle protein 20 (Cdc20) and, possibly, cdc20 homolog 1 (Cdh1) E3 ligase adapters. This activates cyclin-dependent kinase 1/cyclin B1 (CDK1/CYCB1) to directly hyperphosphorylate eukaryotic initiation factor 4E (eIF4E)-binding protein (4E-BP1) at authentic sites, generating a mitosis-specific, mechanistic target of rapamycin (mTOR) inhibitor-resistant δ phospho-isoform not present in G1-arrested cells. Recombinant 4E-BP1 inhibits capped mRNA reticulocyte translation, which is partially reversed by CDK1/CYCB1 phosphorylation of 4E-BP1. eIF4G binding to the eIF4E-m 7 GTP cap complex is resistant to mTOR inhibition during mitosis but sensitive during interphase. Flow cytometry, with and without sT, reveals an orthogonal pH3 S10+ mitotic cell population having higher inactive p4E-BP1 T37/T46+ saturation levels than pH3 S10interphase cells. Using a Click-iT flow cytometric assay to directly measure mitotic protein synthesis, we find that most new protein synthesis during mitosis is cap-dependent, a result confirmed using the eIF4E/4G inhibitor drug 4E1RCat. For most cell lines tested, cap-dependent translation levels were generally similar between mitotic and interphase cells, and the majority of new mitotic protein synthesis was cap-dependent. These findings suggest that mitotic cap-dependent translation is generally sustained during mitosis by CDK1 phosphorylation of 4E-BP1 even under conditions of reduced mTOR signaling.
Merkel cell | small T | 4E-BP1 | cyclin-dependent kinase 1 | mitosis E ukaryotic initiation factor 4E (eIF4E)-binding protein (4E-BP1) is a principal target for mechanistic target of rapamycin complex 1 (mTORC1) (1)(2)(3). mTOR regulates a variety of metabolic signaling pathways related to ribosomal biosynthesis and autophagy that contribute to cancer cell survival (1,(3)(4)(5)(6). Increasing evidence indicates that direct mTORC1 phosphorylation of 4E-BP1 may be the key event in mTOR-associated tumorigenesis (2). In the absence of activated mTOR, hypophosphorylated 4E-BP1 sequesters eIF4E to prevent assembly of eIF4F complex components onto capped mRNA, inhibiting cap-dependent translation. When 4E-BP1 is phosphorylated by mTOR (7), first at critical priming threonine (T) 37 and T46 residues and then at other sites, 4E-BP1 is inactivated and releases eIF4E to allow initiation of cap-dependent translation (8). Other non-mTOR kinases, including cyclindependent kinase 1 (CDK1), have been shown to be able to phosphorylate 4E-BP1 (9-12) but have not been extensively examined in vivo for their effects on 4E-BP1-regulated capdependent translation. Protein synthesis has been described to decrease during mitosis relative to interphase in reports dating back to the 1960s (13,14). There are two issues, however, with this conclusion: (i) Mitotic cells represent less than 1% of the total cell population in bulk culture, and even under stringent conditions, high levels of interphase cell contamination can occur. (ii) Many studies of mitotic cap-dependent translation rely on cell cycle synchronization studies with microtubule inhibitors (e.g., nocodazole), which are also mitotic translation inhibitors (15). Under these conditions, comparisons of interphase and mitotic translation can be imprecise. Single-cell measurements, such as flow cytometry, can potentially overcome these concerns. Additionally, a highly hyperphosphorylated 4E-BP1 isoform called δ-4E-BP1 is present in mitotic cells (10,16). This hyperphosphorylated isoform is predicted to promote rather than inhibit cap-dependent protein translation and is therefore inconsistent with the standard model.

Significance
Cancer cell proliferation is highly dependent on cap-dependent protein synthesis, which is generally assumed to be inhibited during mitosis. Using a viral oncoprotein that enforces mitosis, we show that CDK1 substitutes for mTOR interphase functions to phosphorylate eukaryotic initiation factor 4E-binding protein (4E-BP1) to a mitosis-specific δ isoform. Flow cytometric assays reveal that mitotic cells have high levels of inactivated 4E-BP1 and do not generally show specific loss of cap-dependent translation compared with interphase cells. This appears to be due to cyclin-dependent kinase 1 (CDK1) activity during mitosis. Mitotic cells typically represent less than 1% of all cells in bulk culture, and mitosis-arresting drugs, such as nocodazole, can directly inhibit mitotic protein translation, potentially explaining differences between our findings and previous studies showing reduced cap-dependent translation during mitosis.
Surprisingly, sT-induced δ-4E-BP1 hyperphosphorylation is not dependent on mTOR activity (21). The sT LSD region is known to bind the Fbw7 E3 ligase to promote cell proliferation, but Fbw7 targeting is not sufficient to explain either cell transformation or 4E-BP1 hyperphosphorylation (24).
We show here that MCV sT, through its LSD domain, also promotes mitogenesis and 4E-BP1 hyperphosphorylation by functioning as a promiscuous E3 ligase inhibitor that targets cellular anaphase-promoting complex/cyclosome (APC/C) E3 ligase activity. During sT-induced mitosis, sT-induced CDK1/CYCB1 rather than mTOR directly phosphorylates 4E-BP1 to the mitosis-specific δ isoform. Using a flow cytometry-based method to directly measure mitotic cap-dependent protein synthesis for the first time, to our knowledge, we do not detect a general shift from cap-dependent to cap-independent protein translation in mitotic cells compared with interphase cells. Mitotic cells actually show higher saturation levels of p4E-BP1 T37/T46+ , consistent with 4E-BP1 inactivation, than interphase cells. Consistent with this, and in contrast to previous studies, we find that δ-4E-BP1-positive mitotic cells show high levels of cap-dependent protein translation that is reduced by the cap translation inhibitor 4E1RCat. When accentuated or sustained, high levels of mitotic cap-dependent protein translation may play a role in cancer cell transformation and contribute to mTOR inhibitor resistance in subsets of cancers.

MCV sT Increases Mitogenesis by Targeting the Cellular APC E3 Ligase.
To search for factors contributing to MCV sT-induced transformation, the viral oncoprotein was expressed in hTERTimmortalized primary BJ-tert (BJ-T) human foreskin fibroblasts. These cells displayed a rounded phenotype in culture with increased phospho-histone H3 serine 10 (pH3 S10 ) phosphorylation, characteristic for mitosis (Fig. 1A). Increased pH3 S10 and increased expression of mitotic markers [including cyclin B1 (CYCB1) and phospho-aurora kinase B (pAURKB)] were also observed in 293 cells expressing MCV sT (Fig. S1). Immunoprecipitation of sT revealed an in vivo complex with the APC/C substrate recognition subunit cell division cycle protein 20 (Cdc20) that was dependent on an intact LSD (Fig. 1B). MCV sT also interacted with another APC/C substrate recognition subunit, cdc20 homolog 1 (Cdh1), but substantial Cdh1 binding occurred with sT mLSD having alanine substitutions at residues 91-95, suggesting that sT may bind Cdh1 at other sites in addition to the LSD. In line with these results, known APC/C E3 targets, including AURKA and AURKB, Skp2, polo-like kinase 1 (Plk1), and CYCA2, showed markedly reduced turnover in the presence of sT on cycloheximide (CHX) immunoblotting (Fig.  1C). These APC/C E3 targets retained rapid turnover in the presence of empty vector or sT mLSD expression. CYCD1, which is not directly regulated by APC/C (27), was unaffected by MCV sT or sT mLSD expression. Similarly, MCV sT expression stabilized FLAG-tagged AURKA and endogenous CYCB1, but not CYCD1, after nocodazole release of 293 cells, whereas MCV sT mLSD expression did not (Fig. S2).
Evidence that CDK1 is responsible for δ-4E-BP1 mitotic phosphorylation was also obtained by treatment of nocodazole-arrested HeLa cells with the CDK1 inhibitor RO-3306 (Fig. S3A). δ-4E-BP1 hyperphosphorylation could not be fully restored by RO-3306/ MG132 cotreatment. A technical issue in using mitotic kinase inhibitors to assess 4E-BP1 phosphorylation is the occurrence of mitotic slippage, a side effect of kinase inhibition concurrently causing enforced exit from mitosis with general loss of mitotic kinase activities (30,31). Mitotic slippage can be prevented by simultaneous inhibition of APC/C-mediated protein degradation with the proteasome inhibitor MG132, which in effect "freezes" the mitotic phenotype. Like RO-3306, treatment of nocodazolearrested HeLa cells with the AURK inhibitor VX-680 also eliminated δ-4E-BP1 phosphorylation (Fig. S3B). Unlike RO-3306, however, this was completely reversed by cotreatment with VX-680/ MG132, suggesting that AURK inhibition effects on 4E-BP1 phosphorylation are due to mitotic slippage. Extensive in vitro phosphorylation studies also failed to reveal evidence for direct 4E-BP1 phosphorylation by purified AURKB. To confirm direct 4E-BP1 phosphorylation by CDK1/CYCB1, we generated an in vitro phosphorylation reaction using purified CDK1/CYCB1 and GST-4E-BP1 (Fig. 3B). CDK1 phosphorylation of 4E-BP1 was ATP-dependent and -inhibitable by RO-3306. CDK1 phosphorylation occurred at the previously described T70 residue (10) as well as at authentic 4E-BP1 phosphorylation sites, including T37/T46 and S65/S101, which are known to regulate 4E-BP1 binding to eIF4E.
To confirm these findings in the absence of chemical inhibitors, we used mechanical shake-off to isolate mitotic cells from sT-expressing BJ-T cells (Fig. S4). This maneuver enriched the mitotic cell fraction from ∼2% to ∼66% as determined by flow cytometry with propidium iodide (PI) and pH3 S10 staining (Fig.  S4A). Shake-off cells exclusively expressed the δ-4E-BP1 isoform, whereas adherent cells expressed only α-γ isoforms of 4E-BP1 (Fig. S4B). In vitro lambda phosphatase treatment of sT-expressing and nocodazole-arrested 293 cell lysates showed that the high-molecular-mass 4E-BP1 isoforms, including the α-γ and δ isoforms, are formed as a result of phosphorylation rather than another type of posttranslational modification (Fig. S5).

CDK1/CYCB1 Activates Cap-Dependent Translation During Mitosis.
According to the existing model for 4E-BP1-regulated protein synthesis, high levels of p4E-BP1 T37/T46 are predicted to promote cap-dependent translation during pH3 S10+ mitosis (35). We directly examined this by using cap-binding assays for mitosis-enriched  and -depleted cells and by using a flow cytometry method designed to directly measure single-cell cap-dependent protein synthesis. We performed m 7 GTP cap resin pulldown assays to assess the functional correlates of our flow cytometry and immunoblot findings. Highly enriched mitotic BJ-T cells expressing MCV sT, isolated by shake-off (nonadherent), showed m 7 GTP cap binding to eIF4G that was unaffected by PP242 treatment (Fig. 5A). In contrast, although interphase-enriched BJ-T cells (adherent) had comparable levels of eIF4G, eIF4G cap binding remained sensitive to PP242. Input 4E-BP1 protein from mitosis-enriched cells was almost exclusively in the δ-4E-BP1 isoform. This is consistent with mTOR-independent cap binding during mitosis and mTOR-dependent cap binding during interphase. Qualitatively similar results were found for HeLa cells using G2/M arrest enrichment and shake-off (Fig. S8). For mitosis-enriched HeLa cells, modest but reproducible reduction in eIF4G-m 7 GTP cap association was present with RO-3306 treatment alone but not PP242 treatment alone. Combined RO-3306 and PP242 treatment nearly eliminated eIF4G association to m 7 GTP. These results were confirmed by metabolic labeling using the Click-iT methionine analog L-azidohomoalanine (AHA) to measure nascent protein synthesis (36) (Fig. 5B). In this assay, cells were incubated with AHA for 90 min, in the absence or presence of PP242, in methionine-depleted medium and then subjected to mitotic shake-off. Newly synthesized protein was then labeled with Alexa Fluor 488-alkyne by the copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition (Click-iT) reaction (37) and measured by flow cytometry. Costaining for pH3 S10 allowed segregation of individual cells into "mitotic" (pH3 S10+ ) and "interphase" (pH3 S10-) populations. Up to 74% of DMSO-treated mitotic cells were AHA positive in comparison with 91% of DMSO-treated interphase cells with AHA positivity. PP242 treatment reduced new protein synthesis for pH3 S10interphase BJ-T cells but had no effect on protein synthesis for pH3 S10+ mitotic BJ-T cells (Fig. 5B). Similar analyses using double thymidine block and release synchronization of 293 cells, however, revealed that PP242 reduced new protein synthesis for both mitotic and interphase cells (Fig. S9), suggesting that PP242 resistance may be cell line specific.
Measurement of cap-dependent protein synthesis during mitosis was directly determined for HeLa and U2OS cells after G2 release and synchronization using our AHA assay in cells treated with 4E1RCat (Fig. 5D). Costaining for pH3 S10 allowed segregation of cells into mitotic (pH3 S10+ ) and interphase (pH3 S10-) populations. Nonspecific AHA incorporation was determined using the ribosome translation elongation inhibitor CHX (Fig.  5D, vertical lines), and new protein synthesis was reflected by AHA fluorescence above this baseline.
Like BJ-T cells, fewer (27%) mitotic HeLa cells were positive for new protein synthesis compared with interphase (46%) HeLa cells (Fig. 5D). In contrast, percentages of mitotic and interphase U2OS cells with new protein synthesis were identical (42% of mitotic and interphase cells). For both cell lines, however, nearly all new protein synthesis in both mitosis and interphase was capdependent and -sensitive to 4E1RCat treatment. Preliminary analyses revealed that MG132 treatment nonspecifically inhibited protein synthesis as previously reported (41), preventing us from accurately measuring the effects of CDK1 inhibition on mitotic translation under conditions that inhibit mitotic slippage. Using direct AHA uptake, however, we could confirm that nocodazole treatment specifically inhibits mitotic protein synthesis (Fig. S10).

Discussion
Tumor viruses have been central to cell biology because their oncogenes allow interrogation of specific cell proliferation and survival pathways. Among many critical findings, viral oncoproteins have been essential to the discovery of cellular oncogenes (42) and the tumor suppressor p53 (43)(44)(45), the characterization of the G1/S checkpoint (46) and the Akt-mTOR pathway (47), and identification of common innate immune and tumor suppressor signaling networks (48). MCV sT, an oncoprotein for MCC, induces mTORresistant 4E-BP1 hyperphosphorylation and cell transformation (21), which led us to investigate mTOR-independent 4E-BP1 signaling and cap-dependent translation in mitosis.
In addition to targeting Fbw7 (24), MCV sT inhibits APC/C E3 ligases and induces mitogenesis in sT-expressing cells. One consequence of this is increased mitotic CDK1/CYCB1 activity that is responsible for 4E-BP1 phosphorylation and δ-4E-BP1 formation. Caution is appropriate in interpreting our data, as mitotic kinase inhibition can cause mitotic slippage and exit from the mitotic phenotype. Considerable effort by our group was devoted to evaluating AURKA and AURKB as potential 4E-BP1 mitotic kinases, because AURK inhibitors (e.g., VX-680, MK-5108, and AZD-1152) also reduce 4E-BP1 hyperphosphorylation during mitosis. This was reversible, however, by cotreatment with MG132 to prevent APC/C-mediated mitotic egress, and we have no evidence that AURKs are directly responsible for 4E-BP1 phosphorylation.  Fig. 4. 4E-BP1 is hyperphosphorylated to the δ phosphoisoform during mitosis. (A) pH3 S10+ mitotic 293 cells have higher levels of p4E-BP1 T37/T46+ saturation than cells in other portions of the cell cycle. Dual flow cytometry staining for pH3 S10 and p4E-BP1 T37/T46 was performed on 293 cells synchronized by double-thymidine block and release, which have peak mitotic entry at 10 h postrelease (see also Fig. S6). Vertical bar represents the centroid for p4E-BP1 T37/T46+ fluorescence staining at time 0 h. To determine if 4E-BP1 phosphorylation depends on mTOR activity, cells were also treated 1 h before harvesting with 5 μM PP242. Mitotic cells formed an orthogonal pH3 S10+ / p4E-BP1 T37/T46+ population having high levels of inactivated (phosphorylated) 4E-BP1 that were not dependent on mTOR activity. In contrast, interphase pH3 S10cells were largely mTOR inhibition-sensitive. PP242 treatment increases mitotic entry at 8 h postrelease. (B) PP242-resistant δ-4E-BP1 is formed during peak mitotic entry. Protein lysates were collected from cells in A and immunoblotted for p4E-BP1 and pH3 S10 . Representative results are shown from three independent experiments.
In contrast, there is considerable evidence from this study and others (10,16) to indicate that CDK1/CYCB1 is a bona fide kinase for 4E-BP1.
This study suggests an alternative pathway for CDK1/CYCB1regulated cap-dependent translation during mitosis (Fig. 6). We find that mitotic 4E-BP1 is highly phosphorylated at the priming residues T37 and T46 in pH3 S10+ cells, which runs counter to what would be predicted if cap-dependent translation is reduced during mitosis through an mTOR-related mechanism. The highmolecular-mass δ-4E-BP1 isoform is specific to mitosis, and our data indicate that this results from CDK1-mediated phosphorylation. Although δ-4E-BP1 can form under mitotic conditions in which mTOR is inhibited, it seems likely that mTOR cooperates with CDK1/CYCB1 to generate the mitotic δ-4E-BP1 by phosphorylating lower molecular mass α-γ isoforms that may be precursors to the δ-4E-BP1 isoform. Another limitation to our study is that we measure only 4E-BP1 phosphorylation but not δ-4E-BP1 dephosphorylation or turnover. These are likely to affect steady-state p4E-BP1 levels as well.
Our findings contrast with studies suggesting that loss of mTOR activity leads to inhibition of mitotic eIF4G cap-association and capdependent translation. We see cap-dependent protein translation is sustained during mitosis using a pulse flow cytometry approach. Pharmacological (4E1RCat) cap-dependent translation inhibition provides evidence that this effect is generalizable. AHA pulse labeling allows direct measurement of translation in mitotic cells, which avoids confounding issues stemming from bulk culture measurements. Although most mitotic translation was cap-dependent in all of the cell lines tested by AHA uptake, differences in relative mitotic and interphase translation were present between cell lines. Like [ 35 S]methionine incorporation studies, AHA incorporation measurements require incubation of cells in low-methionine media.
We suspect that technical issues, which have only recently been resolved, explain differences between our studies and those of others. Measurement of mitotic protein translation (both capdependent and -independent) has relied on separation of mitotic and interphase cells in bulk culture, often using nocodazoleinduced mitotic enrichment. We confirm that nocodazole inhibits mitotic translation for synchronized 293 cells. This has been ascribed by Coldwell et al. (15) to inhibitory phosphorylation of eIF2 and eIF4GII by nocodazole downstream to 4E-BP1 regulation. This is consistent with our findings that nocodazole both promotes δ-4E-BP1 and inhibits mitotic translation. We have not tested other mitotic-arrest compounds (e.g., paclitaxel) to determine if  formation on the m 7 GTP cap is PP242-independent for mitosis-enriched cells but PP242-sensitive for mitosis-depleted cells. BJ-T cells expressing MCV sT were harvested by mitotic shake-off to enrich for mitotic (nonadherent) and nonmitotic (adherent) populations and compared with asynchronous empty vector BJ-T cells without shake-off. Lysates were bound to m 7 GTP-resin, precipitated, and immunoblotted. Mitosis-enriched cell eIF4G binding, as well as 4E-BP1 binding, to the eIF4E/cap complex was unaffected by mTOR inhibition. For mitosis-depleted cells, eIF4G binding was reduced and 4E-BP1 binding was increased by mTOR inhibition. Representative results from two independent experiments are shown. (B) Nascent protein synthesis during mitosis is resistant to mTOR inhibition in BJ-T cells. BJ-T cells stably expressing sT were labeled with AHA for 45 min in methionine-depleted media, separated by mitotic shake-off as in A, reacted with Click-iT Alexa Fluor 488 alkyne after permeabilization, and new protein synthesis was measured by flow cytometry. Relative mitotic protein synthesis was determined by dividing percentage of pH3 S10+ -AHA + cells by percentage of total pH3 S10+ cells. Likewise, interphase protein synthesis was determined by dividing percentage of pH3 S10--AHA + cells by percentage of total pH3 S10cells. Approximately 91% of pH3 S10adherent interphase cells showed AHA incorporation that was sensitive to mTOR inhibition. Only 74% of pH3 S10+ -positive mitotic cells were positive for AHA uptake, but this new protein synthesis was resistant to PP242 treatment. Baseline fluorescence was determined in asynchronous BJ-T cells without AHA incubation. I, interphase pH3 S10cells; M, mitotic pH3 S10+ cells. (C) In vitro capped mRNA translation is inhibited by 4E1RCat and activated by CDK1/CYCB1. Capped and polyadenylated luciferase mRNA was generated in a T7 polymerase reaction and used to produce luciferase protein in rabbit reticulocyte lysate. The addition of 4E1RCat abolished luciferase translation, whereas addition of GST-4E-BP1 reduced translation to 15% of buffer control (averages for three independent experiments with SEM shown). When GST-4E-BP1 was phosphorylated by CDK1/CYCB1 in kinase reaction buffer, translation increased to 43% of buffer control. This effect was eliminated by RO-3306 pretreatment. Insert shows GST-4E-BP1 phosphorylation immunoblot. (D) Mitotic translation is primarily cap-dependent for HeLa and U2OS. HeLa or U2OS cells were synchronized for 24 h at the G2/M boundary with RO-3306 (10 μM), released by washing, and incubated with 25 μM of AHA for 90 min in methionine-depleted media, and then harvested 2 h after release. Harvested cells were permeabilized and reacted with Alexa Fluor 488 alkyne to measure AHA incorporation into protein. DMSO vehicle control, CHX (100 μg/mL), or 4E1RCat (50 μM) were added together with AHA 30 min after release. Vertical bar represents maximum AHA incorporation after CHX translation inhibition. Fewer mitotic (26%) than interphase (42%) HeLa cells were positive for new protein synthesis, but all cells were sensitive to 4E1RCat inhibition of cap-dependent translation. For U2OS, cell numbers positive for total mitotic and interphase translation were identical (42%), and cap-dependent translation represented 73% and 85% of mitotic and interphase translation, respectively. Bottom panel shows 4N-gated AHA positivity for treated cells, which shows that 4E1RCat inhibition (cap-dependent) is similar to CHX (total) translation inhibition. Representative results are shown for one of three independent experiments. they have similar limitations. A second technical challenge is that mitotic cells represent a small fraction of the total cell population. Contamination with interphase cells is nearly inevitable in mitotic enrichment protocols and will dramatically alter conclusions, such as the role of mTOR in regulating 4E-BP1 during mitosis. In our experience, flow cytometry can help to resolve this dilemma by directly measuring mitotic status (pH3 S10 or pMPM2 status) in cells while simultaneously determining translation regulator status, such as p4E-BP1 T37/T46 . Finally, newly developed classes of cap-dependent translation inhibitors such as 4E1RCat now allow direct determination of cap-dependent translation. When used in combination with AHA incorporation, direct measurement of mitotic cap-dependent translation can be determined.
Both nocodazole and PP242 are nonetheless important inhibitors to measure 4E-BP1 phosphorylation and translation during mitosis. As indicated, nocodazole does not interfere with δ-4E-BP1 formation and is useful for accentuating mitotic regulation of 4E-BP1. mTOR regulates translation through ribosomal biosynthesis as well as direct phosphorylation of translation machinery components downstream from 4E-BP1, such as eIF4B (49) and eEF2 elongation factor (50). Further, eIF4B regulation by 14-3-3σ may also play a role in later stages of mitotic protein translation and may be missed in our study of early mitosis (51). Thus, PP242 may affect mitotic translation by acting downstream to 4E-BP1. We also find evidence that in most cells mTOR typically acts in concert with CDK1/CYCB1 to promote mitotic cap-dependent translation.
Cap-dependent translation of preformed mRNAs provides rapid regulation of gene expression that may be required for short-lived cellular responses, such as transit through mitosis. These changes generally cannot be accurately measured by standard mRNA expression techniques. Mounting evidence suggests that dysregulated cap-dependent translation from aberrant PI3K-Akt-mTOR and MEF-RAF-MEK-ERK signaling contributes to cancer cell transformation (3,52). Regardless of the contribution of activated cap-dependent translation to cancer cell transformation, such as in MCV-positive MCC, our findings point toward the possibility that combined mTOR and CDK1/CYCB1 inhibition may prove useful for cancer treatment, particularly for mTOR inhibitor-resistant cancers.

Materials and Methods
Plasmids, antibodies, primers, and standard methods are described in SI Materials and Methods.
Flow Cytometry. The 293 and BJ-T cells were trypsinized and fixed in 70% (vol/vol) ethanol for DNA staining or in 10% (vol/vol) buffered formalin for AHA incorporation assays. Fixed cells were washed with PBS containing 1% FBS and permeabilized with 0.25% Triton X-100 for 30 min on ice. For cell cycle analysis, cells were resuspended in PI/RNase staining solution (0.05 mg/mL PI, 0.1 mg/mL RNase A in 1× PBS) and incubated for 30 min at room temperature. For phospho-histone H3 S10 and phospho-4E-BP1 T37/T46 analysis, cells were incubated with the corresponding fluorophore-conjugated antibodies for 2 h at room temperature.
Cell Cycle Synchronization and Mitotic Cell Enrichment. The 293 cells were treated with medium containing 0.5 μM nocodazole or 0.5 mM L-mimosine for 16 h to induce mitotic arrest or G1 arrest, respectively. Mitotic cells were enriched by double-thymidine block (2 mM) and release using 293 and U2OS cells or by mitotic shake-off (53) using BJ-T cells stably expressing wild-type MCV sT. To block the cell cycle at late G2, HeLa and U2OS cells were incubated in medium containing CDK1 inhibitor RO-3306 (10 μM) for 24 h. Cell cycle entry from G2 to mitosis was induced by RO-3306 washout. Cells arrested by nocodazole and released from RO-3306 arrest were treated with 10 μM of proteasome inhibitor MG132 for 30 min before kinase inhibitor treatment to retain cells in mitosis.
Kinase Inhibitors. The following active-site kinase inhibitors were dissolved in DMSO and used for in vivo kinase inhibition and in vitro phosphorylation experiments: mTOR kinase inhibitor PP242 (Selleckchem), CDK1 kinase inhibitor RO-3306 (Calbiochem), and pan Aurora kinase inhibitor VX-680 (Selleckchem).
In Vitro Phosphorylation Assays. Recombinant GST-4E-BP1 (0.2 μg) (Signal-Chem) was incubated in a 24-μL reaction containing 1× protein kinase buffer (NEB) and 20 units of recombinant CDK1/CYCB1 (NEB) or 10 μg of mitotic HeLa cell lysate, supplemented with 200 μM ATP and/or 5 μM active site kinase inhibitors, for 30 min at 30°C. HeLa cells were arrested in mitosis by treatment with 0.5 μM nocodazole for 16 h and enriched by mechanical shake-off for lysis in nondenaturing lysis buffer (50 mM Tris•HCl, pH 7.4, 0.15 M NaCl, 1% Triton X-100, 2 mM Na 3 VO 4 , and 2 mM NaF). The reactions were stopped by adding 5× SDS sample buffer to 1× concentration and boiling for 5 min. Reaction samples were then subjected to SDS/PAGE and immunoblotting. For in vitro protein dephosphorylation, 293 cell extracts were incubated with lambda phosphatase in protein metallophosphatase reaction buffer (NEB) supplemented with 2 mM MnCl 2 for 30 min at 37°C. Reactions were stopped by adding 2× SDS sample buffer and then subjected to SDS/ PAGE and immunoblotting. m 7 GTP Cap-Binding Assay. Shake-off (mitosis-enriched) and adherent cells (mitotic-depleted) from MCV sT-transduced BJ-T cells or asynchronous BJ-T cells were lysed in buffer (50 mM Tris·HCl, pH 7.4, 0.15 M NaCl, 1% Triton X-100, 2 mM Na 3 VO 4 , and 2mM NaF) supplemented with protease inhibitors (Roche). Lysates (30 μg of total protein) were incubated with 5.0 μL of m 7 GTP Sepharose beads (GE Healthcare) overnight at 4°C. Beads were collected, washed with lysis buffer, and subjected to SDS/PAGE and immunoblotting. We loaded 25 μg of total protein as input control (83%).
In Vitro mRNA Synthesis and Translation. Capped firefly-luciferase (FLuc) reporter mRNA was synthesized by the MessageMAX T7 ARCA-Capped message transcription kit (Cell Script) using 1 μg pCD-V5-FLuc linearized by MscI as template. pCD-V5-Fluc was constructed by ligating FLuc from pGL3 to pCDNA6/V5-HisB between Hind II and XbaI. Purified RNA was polyadenylated using the A-Plus Poly (A) polymerase tailing kit (Cell Script). Translation reactions were performed in a final volume of 10 μL consisting of 7 μL of nuclease-treated RRL (Promega), 0.8 pmol of capped and polyadenylated reporter mRNAs, and an amino acid mixture (50 μM each). GST-4E-BP1 was incubated with either CDK1 or 1 μg/mL BSA in the presence of DMSO or 10 μM RO-3306 (see reaction setup for previous section). As a control, PBS alone was incubated with the same amount of either DMSO or 10 μM RO-3306. Either buffer or pretreated GST-4E-BP1 (12.4 μL) was added to the RRL reaction mixture. The prepared RRL mixture was incubated for 15 min at 30°C. The
Nascent Protein Synthesis Analysis. BJ-T sT stable cells were labeled with an azide-linked methionine analog AHA (Life Technologies) at 25 μM for 45 min in the presence or absence of PP242 (5 μM), followed by mitotic shake-off to separate mitotic cells and interphase cells. To analyze mitotic cap-dependent translation in U2OS and HeLa cells, cells were arrested at the G2/M boundary by 10 μM RO-3306 treatment for 24 h (34). After 30 min of RO-3306 removal, cells were labeled with AHA (25 μM) for 90 min in methionine-depleted DMEM (Corning Cellgro) after optimization of preexperiments. Translation inhibitors [4E1RCat (50 μM) or CHX (100 μg/mL)] or DMSO (0.1%) were added to cells with AHA. Cells were trypsinized and fixed in 10% (vol/vol) formalin for 5 min. Fixed cells were permeabilized in PBS containing 0.1% saponin and 1% FBS for 30 min at room temperature. Cells were harvested and labeled with the Alexa Fluor 488 alkyne using the Click-iT cell reaction buffer kit (Life Technologies). AHA incorporation in cells was analyzed by flow cytometry as a measure for nascent protein synthesis in interphase and mitotic cells.
Statistic Analysis. One-sided t test was performed for densitometric analysis of m 7 GTP pulldown assays and two-sided t test (unequal variances) for in vitro translation assays. A P value less than 0.05 was considered to be significant.