Regulation of CK2 by phosphorylation and O-GlcNAcylation revealed by semisynthesis.

Protein serine-threonine kinase casein kinase II (CK2) is involved in a myriad of cellular processes including cell growth and proliferation through its phosphorylation of hundreds of substrates, yet how CK2 function is regulated is poorly understood. Here we report that the CK2 catalytic subunit CK2α is modified by O-linked β-N-acetyl-glucosamine (O-GlcNAc) on Ser347, proximal to a cyclin-dependent kinase phosphorylation site (Thr344). We use protein semisynthesis to show that phosphorylation of Thr344 increases the cellular stability of CK2α by strengthening its interaction with Pin1, whereas glycosylation of Ser347 seems to be antagonistic to Thr344 phosphorylation and permissive to proteasomal degradation. By performing kinase assays with site-specifically phospho- and glyco-modified CK2α in combination with CK2β and Pin1 binding partners on human protein microarrays, we show that the kinase substrate selectivity of CK2 is modulated by these specific post-translational modifications. This study suggests how a promiscuous protein kinase can be regulated at multiple levels to achieve particular biological outputs.

Introduction

Protein Kinase CK2 (also known as casein kinase II) is a Ser/Thr kinase implicated in cell proliferation and many disease processes[1]. CK2 is ubiquitously expressed and is proposed to phosphorylate hundreds, if not thousands, of distinct cellular protein substrates, but its mechanisms of regulation are poorly understood[2,3]. The 45 kDa catalytic CK2 polypeptide (CK2α) can exist as an active monomer in cells, but it can also phosphorylate substrates when part of a tetrameric complex containing two CK2α and two 25 kDa CK2β subunits[4]. The substrate specificity and catalytic activity of CK2α is reported to be modulated through its association with the CK2β subunit, but this has only been studied for a handful of substrates[5-7]. CK2α is modified by C-terminal phosphorylation on four sites (T344, T360, S362, S370) by Cdk1/cyclin B (Fig.1a), but the role of such phosphorylation on CK2 function is not clear[8,9]. Mutation of these positions to Glu, a rather crude phosphoSer/phosphoThr mimic, has not yielded an obvious change in activity.

Figure 1

Preparation of CK2α semisynthetic proteins

(a) The posttranslational modifications on CK2. The known posttranslational modifications on CK2α include: phosphorylation at positions Thr344, Thr360, S362, S370 and lysine acetylation at K102[50]. Here we demonstrate CK2α is O-GlcNAc modified at Ser347. (b) Scheme for expressed protein ligation and list of the peptides used for semisynthesis. (c) Posttranslational modifications and the cleavage-resistant mimics used.

In many instances, nuclear, cytoplasmic, and mitochondrial proteins can be modified dynamically by O-linked β-N-acetyl-glucosamine (O-GlcNAc) at or near sites of phosphorylation[10,11]. The addition of O-GlcNAc to protein Ser/Thr residues is receiving increasing attention in cell signaling studies as more of these sites are mapped[11-14], but it has generally been difficult to elucidate the detailed functions of these modifications at specific sites. Classical mutagenesis of the specific sites modified and/or inhibition of O-GlcNAc transfer enzymes by drugs or RNAi have been standard techniques to analyze O-GlcNAcylation, but they lack the precision needed to pinpoint biochemical effects of particular PTMs (posttranslational modifications). In fact, the same challenges pertain to sorting out phosphorylation-site specific effects.

As discussed below, we reveal here that CK2α is O-GlcNAc-modified on Ser347, near the Cdk1/cyclin B-mediated Thr344 phosphorylation site. Protein semisynthesis[15] is used in this study to install metabolically stable O-GlcNAc equivalent, S-GlcNAc-, and phosphonate, Pfa, mimics site-specifically into CK2α. Furthermore, the effects of these modifications on kinase activity, substrate selectivity, as well as cellular stability have been analyzed. We show that phosphorylation at Thr344 appears to stabilize CK2α by enhancing Pin1 interaction. In contrast, O-GlcNAcylation at Ser347 inhibits Thr344 phosphorylation and reciprocal CK2α phosphorylation and O-GlcNAcylation modulate protein kinase substrate selectivity.

Results

CK2α is O-GlcNAc modified at Ser347

Although it has been shown that O-GlcNAc transferase (OGT) can modify CK2 in vitro[11,14], it has not been previously reported that CK2α is O-GlcNAc modified in cells. We purified CK2α from bovine brain, fractionated it on a WGA column, and tested fractions for CK2 activity (Supplementary Results, Supplementary Fig. 1a). We found that fractions that bound to the column and eluted with 0.5M GlcNAc contained the highest CK2 activity, suggesting that a majority of the active CK2 protein is modified by terminal GlcNAc or sialic acid residues. We used reaction with UDP-[3H]galactose and galactosyltransferase to probe for terminal GlcNAc residues and demonstrated that CK2α but not CK2β, contains terminal GlcNAc residues (Supplementary Fig. 1b). The radiolabel was lost when we subjected the samples to alkali-induced β-elimination, consistent with an O-glycosidic bond to Ser/Thr. We found that sizing of the released saccharide by chromatography matched standard Galβ1,4GlcNAcitol disaccharide, which is the expected product for a single GlcNAc residue labeled by galactosyltransferase and galactose. Using cyanogen bromide cleavage followed by HPLC purification of peptides and Edman sequencing, we identified Ser347 as the CK2α O-GlcNAc modification site, a position that is close to one of the phosphorylation sites (Thr344) in the C-terminal tail of CK2α (Supplementary Fig. 1c,d).

CK2α semisynthetic protein preparation

To investigate the potential functions of Thr344 phosphorylation and Ser347 O-GlcNAcylation, we generated modified and unmodified CK2α semisynthetic proteins using expressed protein ligation[16-18]. For this strategy, we expressed in E. coli an N-terminal recombinant CK2α protein fragment (residues 1–341, with or without an N-terminal hemagglutinin (HA) epitope tag) bearing a C-terminal thioester using an in-frame intein. In addition, we synthesized N-Cys containing peptides (aa 342–365) carrying substitutions of interest at positions 344 (Thr, pThr, or phosphonodifluoromethylene alanine (Pfa)) or 347 (SGlcNAc-Ser or Ser) using solid phase peptide synthesis (Fig. 1b,c and Supplementary Fig. 2)[16-19]. Ligation of the recombinant protein and synthetic peptide fragments proceeded smoothly, and we obtained the desired semisynthetic CK2α proteins in milligram quantities in >95% purity judged by Coomassie-stained SDS-PAGE and MALDI-MS (Supplementary Figs. 3,4). In control experiments, we showed that the necessary introduction of a Cys at position 342 (in place of Gly) and a modest (26 residue) C-terminal truncation of the CK2α relative to the full-length wild-type protein were well tolerated and did not alter the kinase activity with synthetic peptide substrate. Specific kinase activities for semisynthetic unmodified CK2α agreed within 20% of those for the recombinant full-length wild-type and G342C CK2α proteins (see Supplementary Table 1). There were some experiments where either the naturally occurring pThr or Pfa containing proteins were used, but in experiments where both proteins were used, it was demonstrated that Pfa effectively mimics the pThr residue.

Determination of kinetic parameters of CK2α proteins

We analyzed the kinase activities of the Pfa344, S-GlcNAc-Ser347, and unmodified semisynthetic CK2α proteins using three different peptide substrates: an optimized peptide[20], a peptide based on casein[21], and a peptide based on the XRCC1 protein[22]. We determined the apparent kcat and Km values for each of the semisynthetic CK2αs with each peptide substrate and ATP. Turnover numbers for CK2 activity with the optimized substrate were within 2-fold of those previously described[23,24]. As shown in Table 1, there were little or no (<2-fold) changes in the catalytic parameters among the semisynthetic CK2αs bearing different modifications. The role of CK2β on CK2α activity has been investigated previously[6,7,25,26], and we confirm here that it can modulate peptide phosphorylation efficiency (Table 1). For the optimized and casein peptide substrates, there was an increase in Km values in the presence of the CK2β subunit; however, this increase in Km was not impacted by 344 or 347 PTM. These data suggest that the 344 and 347 PTMs in CK2α did not have a significant effect in modulating CK2 catalytic efficiencies (kcat/Kms) with peptide substrates regardless of the presence of CK2β.

Table 1

Kinetic Parameters for CK2 semisynthetic enzymes

Substrate	Enzyme	Apparent kcat(min−1)	Apparent Km(µM)	kcat / Km(min−1 µM−1)
Optimized Peptide	unmodified α	260 ± 10	37 ± 7	7.1
	Pfa α	260 ± 10	33 ± 5	7.8
	S-GlcNAc α	190 ± 10	33 ± 5	5.7
	unmodified α+β	180 ± 20	170 ± 50	1.0
	Pfa α+β	200 ± 20	160 ± 50	1.2
	S-GlcNAc α+β	160 ± 10	160 ± 50	0.90
Casein Peptide	unmodified α	22 ± 1	400 ± 50	0.054
	Pfa α	22 ± 1	340 ± 60	0.065
	S-GlcNAc α	15 ± 1	340 ± 30	0.044
	unmodified α+β	NS	>1600	0.014
	Pfa α+β	NS	>1600	0.015
	S-GlcNAc α+β	NS	>1600	0.013
XRCC1 Peptide	unmodified α	180 ± 10	250 ± 10	0.74
	Pfa α	240 ± 30	350 ± 90	0.69
	S-GlcNAc α	190 ± 10	250 ± 30	0.75
	unmodified α+β	75 ± 4	260 ± 40	0.29
	Pfa α+β	130 ± 20	460 ± 120	0.28
	S-GlcNAc α+β	100 ± 10	440 ± 120	0.24
ATP	unmodified α	320 ± 10a	20 ± 2 a	16
	Pfa α	370 ± 10 a	21 ± 2 a	18
	S-GlcNAc α	270 ± 10 a	16 ± 2 a	17
	unmodified α+β	250 ±20b	39 ± 6b	6.3
	Pfa α+β	250 ± 20b	30 ± 4b	8.3
	S-GlcNAc α+β	190 ± 10b	31 ± 4b	6.2

± values indicate standard error obtained from non-linear curve-fitting parameters. NS = non-saturated with peptide substrate, Km value was not determined. Kmapp peptide and kcat values were obtained with 100 µM ATP.

Kmapp ATP and kcat values were obtained with 360 µM optimized peptide.

Kmapp ATP and kcat values were obtained with 800 µM optimized peptide.

Localization and stability of semisynthetic CK2αs

Prior experiments suggest that mitotic and phosphorylated CK2α might be driven to the cell nucleus[27]. To examine the potential effect of 344-phosphorylation and 347-glycosylation of CK2α on cellular localization, we microinjected N-terminally HA-tagged semisynthetic CK2α proteins containing Pfa344, S-GlcNAc-Ser347, and no modifications into the cytoplasm of rat embryonic fibroblasts (REF52 cells) and performed immunocytochemistry using an anti-HA Ab (Supplementary Figs. 5,6). It should be noted that the Pfa[18] and S-GlcNAc[19] phospho- and glyco-mimics are resistant to enzymatic cleavage[28] which makes them useful for cellular studies. Unexpectedly, there did not appear to be any significant differences in cellular localization (nuclear vs. cytoplasmic) of CK2α due to the different modifications on its C-terminal tail (Supplementary Fig. 5). At 2 h following microinjection in the cytoplasm, much of the CK2α had translocated into the nucleus although there was residual cytoplasmic protein (Supplementary Fig. 5). Interestingly, when CK2β was co-injected with the semisynthetic CK2αs, we found that the CK2α subunit was apparently retarded in moving into the cell nucleus (Supplementary Fig. 5). However, the Pfa- and S-GlcNAc-containing CK2αs behaved the same as unmodified CK2α in this regard (Supplementary Fig. 5). Taken together, our data suggest that phosphorylation at Thr344 site or O-GlcNAcylation at Ser347 does not have a major impact on cellular localization regardless of the presence of the CK2β subunit.

We also carried out microinjection studies to examine the cellular stability of CK2α in response to the different modifications on its tail (Fig. 2a–c and Supplementary Fig. 6). Unexpectedly, the Pfa344-CK2α was significantly more stable than the S-GlcNAc-Ser347 or unmodified CK2αs, most clearly evident 4 and 8 h after microinjection (Fig. 2a and Supplementary Fig. 6). We also observed this enhanced stabilization of CK2α mediated by the phospho-mimetic after co-injection with stoichiometric CK2β, although CK2β slowed the breakdown of S-GlcNAc-Ser347 and unmodified CK2α (Fig. 2b). The idea that degradation of unmodified CK2α is mediated by the proteasome was bolstered by our finding that proteasome inhibitor MG132 led to stabilization of the microinjected kinase (Fig. 2c).

Figure 2

Cellular stability of CK2α

(a) Relative CK2α protein levels over time following cytoplasmic microinjection of REF52 cells with the HA-tagged semisynthetic proteins bearing different modifications using immunocytochemistry with anti-HA Ab. Data represent mean values ± s.d. (b) Relative CK2α protein levels following co-injection of β subunit with CK2α proteins. Data represent mean values ± s.d. (c) Relative CK2α protein levels following co-injection of proteasome inhibitor (1 µM MG132) with unmodified CK2α protein. Data represent mean values ± s.d. (d) Western blot for total CK2α protein in HeLa cells following treatment with Cdk inhibitors. Numbers indicate relative quantification normalized for loading control, mean values (n = 3) shown ± s.d. (e) Western blot for total CK2α protein in HeLa cells following treatment with nocodazole to arrest cells in mitosis. See Supplementary Fig. 8 for full gels corresponding to those in panels d, e.

CK2α cellular stabilization, Cdks, and Pin1 interaction

As shown above, the Pfa phospho-mimic at Thr344 of CK2α protects the kinase from degradation in REF52 cells. To further examine how phosphorylation of CK2α enhances its cellular stability, we analyzed endogenous CK2α protein levels in HeLa cells using Western blots following pharmacologic manipulation predicted to perturb the phosphorylation state of CK2α (Fig. 2d and 2e). Since Cdk1/cyclin B has been reported to be responsible for cellular phosphorylation of CK2α[8], we investigated the effects of two small molecule Cdk kinase inhibitors flavopiridol[29] and 9-cyanopaullone[30] (Fig. 2d and Supplementary Fig. 7). We treated HeLa cells with either flavopiridol or 9-cyanopaullone vs. vehicle (control DMSO) which caused cell cycle changes (Supplementary Fig. 7) consistent with their known broad spectrum Cdk inhibition[31,32] and led to considerable decrease in total CK2α protein levels (Fig. 2e). Prior studies report that the mitotic spindle poison nocodazole can induce a state where CK2α is highly phosphorylated[8,33]. Here we show that HeLa cells treated with nocodazole, which caused G2/M phase arrest (Supplementary Fig. 9), had higher levels of both phosphorylated and total CK2α compared with vehicle-treated cells (Fig. 2e). Taken together, these pharmacologic and microinjection experiments support the concept that phosphorylation by Cdks can stabilize CK2α in the cell.

It has been shown that phosphorylation of CK2α can confer interaction with the phosphoSer/Thr adaptor protein Pin1[34], a peptidyl-prolyl cis/trans isomerase (PPIase) active on only phospho-Ser/Thr-Pro motifs[35]. We thus performed pull-down assays with HA-tagged semisynthetic CK2αs, which demonstrated that only pThr344 CK2α and Pfa344 could efficiently bind Pin1, whereas Thr344, Glu344 (a crude phospho-mimic), and S-GlcNAc-Ser347 showed minimal evidence of Pin1 interaction (Fig. 3a). The concentrations of Pin1 used in our pull-down assays were selected based on estimated Pin1 concentrations in the cell[36]. Co-immunoprecipitation of endogenous Pin1 from REF52 cell lysates with Pfa344 CK2α but not unmodified CK2α provides further evidence for the phosphorylation dependence of this interaction (Fig. 3b). To determine whether this pThr-dependent interaction with Pin1 plays a role in CK2α cellular stability, we evaluated for the impact of polyclonal anti-Pin1 antibody IgY, (which competed for pThr-CK2 binding to Pin1 in vitro, Fig. 3c), on HA-tagged Pfa344 CK2α level after cytoplasmic microinjection in REF52 cells. Indeed, co-injection of anti-Pin1 IgY with Pfa344 CK2α into REF52 cells resulted in degradation of CK2α relative to cells co-injected with Pfa344 CK2α and vehicle or control non-specific IgY Ab (Fig. 3d and Supplementary Fig. 12). These results suggest that disruption of the Pin1/phospho-CK2α interaction was sufficient to eliminate the enhanced cellular stability of CK2α imparted by the presence of Pfa at Thr344.

Figure 3

CK2 interactions with Pin1

(a) Pull-down experiments with semisynthetic HA-CK2α protein and recombinant Pin1. CK2α was immobilized using anti-HA antibodies bound to protein G beads. Pin1 was incubated with immobilized CK2α for 20 min at 4°C. (b) Co-immunoprecipitation of endogenous Pin1 with CK2α. Pfa containing and unmodified HA-CK2α semisynthetic proteins were spiked into REF52 cell lysates and immobilized using anti-HA antibodies. Input samples are shown for loading control. (c) Pull-down experiments with Pfa344 HA-CK2α protein and recombinant Pin1 in the presence of anti-Pin1 or non-specific IgY. (d) Relative CK2α protein levels over time following microinjection of Pfa344 CK2α with anti-Pin1 IgY or non-specific IgY (control). Data represent mean values ± s.d. See Supplementary Figs 10, 11 for full gels corresponding to those in panels a–c.

O-GlcNAc influences phosphorylation and stability of CK2α

The CK2α O-GlcNAc modification (Ser347) lies proximal to its Thr344 phosphorylation site. We thus examined whether the presence of S-GlcNAc at Ser347 can influence the extent to which Thr344 can be phosphorylated by recombinant Cdk1/cyclin B in the context of a synthetic peptide substrate derived from the CK2α C-terminal tail (residues 337–352). Using a 32P-ATP kinase assay, we showed that the peptide containing S-GlcNAc at Ser347 was phosphorylated by Cdk1/cyclin B very weakly compared with the unmodified peptide substrate (Fig. 4a and Supplementary Fig. 13), indicating that the S-GlcNAc group interfered with enzyme-substrate binding, catalysis, or both. To test whether GlcNAc modification could influence phosphorylation-induced stabilization of endogenous CK2α in cells, we examined the pharmacologic influence of selective O-GlcNAcase enzyme inhibitor ThiametG (TMG)[37] in cell culture. First, we showed that addition of TMG (20 µM) for 12 h could enhance the level of O-GlcNAc modification on CK2α from HeLa cells as judged by immunoprecipitation-western blot analysis (Fig. 4b). However, 12–16 h after TMG exposure, there was a modest but reproducible (n=4) reduction in overall CK2α protein amounts as judged by western blot (Fig. 4c). We interpret the results of these experiments as evidence that enhancing CK2α O-GlcNAcylation reduced Cdk-mediated phosphorylation and may have subsequently conferred reduced cellular stability of CK2α.

Figure 4

Role of O-GlcNAc modification in CK2α

(a) Phosphorylation of C-terminal tail CK2α peptides (residues 337 to 352) by Cdk1/cyclin B. In vitro Cdk1/cyclin B kinase assays were performed using the following peptide substrates: SSMPGGSTPVXSANMMK(εBiotin) where X = serine or S-GlcNAc-serine. After reactions were quenched, peptides were separated from reaction mixture on Tris-tricine gels. Data represent mean values ± s.d. (b) IP-Western blot for O-GlcNAc CK2α in HeLa cells following treatment with O-GlcNAcase inhibitor, TMG, for 12 h. Numbers indicate relative quantification normalized for total CK2α levels. (c) Western blot for total CK2α protein in HeLa cells following treatment with TMG for 12 or 16 h. Numbers indicate relative quantification normalized for loading control, mean values (n = 4) shown ± s.d. See Supplementary Figs. 14, 15 for full gels corresponding to those in panel b,c.

CK2 kinase activity with protein substrates

While the work described above establishes that 344 phosphorylation and 347 O-GlcNAcylation of CK2α do not influence CK2’s activity in simple peptide substrate phosphorylation, we considered the possibility that protein substrate selectivity might be more sensitive to CK2α PTMs. Initial support for this idea came from our observation that calmodulin, known to be more efficiently phosphorylated by CK2α monomer versus CK2α:CK2β tetramer[5], showed modestly greater inhibition of phosphorylation by pThr344-CK2α relative to S-GlcNAc-Ser347-CK2α and unmodified CK2α in the presence of sub-saturating CK2β (Supplementary Fig. 16).

To more comprehensively determine the interplay between CK2α PTMs and CK2β effects on catalytic activity, we performed kinase assays on a home-made microarray of 17,000 human proteins fabricated using the same method as described previously[38]. Using the standard deviation (SD) from the normal distribution of the signal intensities of all of the proteins, we used a stringent cutoff of three SDs to identify positive hits. The initial set of CK2 kinase assays on the microarray identified approximately 200 substrates that were phosphorylated on duplicate microarrays by at least one of the CK2 enzyme forms tested (unmodified CK2α ±β, S-GlcNAc CK2α ±β, Pfa CK2α ±β) (Supplementary Fig. 17). Proteins identified as “positive hits” in both duplicate experiments were qualified as a “substrate” for a given experiment. The results of these kinase assays on the microarray were computationally validated by statistical analysis that demonstrated enrichment for known CK2 substrates (see Supplementary Tables 2 and 3)[3,39].

Of the substrates identified in the microarrays, 23 proteins could be classified as substrates that were selectively phosphorylated by specific PTM forms of CK2. These are listed in Table 2. To be included in Table 2, the “positive hit” could not have shown to be positive in either of the duplicate experiments for the other CK2 enzyme forms. For example, AHCYL2 was phosphorylated in duplicate on both microarrays treated with S-GlcNAc CK2α+β, but not on any of the microarrays treated with the other CK2 enzyme combinations. There were also examples of substrates whose phosphorylation by CK2 was inhibited by the presence of a PTM. PCDL2 was phosphorylated in duplicate on both microarrays treated with unmodified CK2α as well as both microarrays treated with Pfa344 CK2α, but not phosphorylated on either microarray treated with S-GlcNAc-Ser347 CK2α. To confirm the findings with microarrays, we selected several of these substrates, expressed and purified them on a larger scale (Supplementary Fig. 18), and tested them in solution phase kinase assays. Consistent with the protein microarray results, the S-adenosylhomocysteine hydrolase homolog AHCYL2 was most efficiently phosphorylated by S-GlcNAc-Ser347-CK2α in the presence of CK2β compared to all five other combinations (Fig. 5a). In contrast, the histone chaperone NAP1L3 was most effectively phosphorylated by pThr344 (and Pfa344) CK2α in the presence of CK2β relative to the other five possibilities, as observed in the microarray experiments (Fig. 5b). Interestingly, the T344E mutant could not substitute adequately for the pThr344 or Pfa344 protein, indicating a role for the authentic PTM or its close phosphonate mimic (Pfa) for achieving NAP1L3 substrate specificity (Supplementary Fig. 20). Other recombinant protein solution phase kinase assays that recapitulated protein microarray results included eEF-2 kinase and WASL (best phosphorylated by O-GlcNAc- and unmodified CK2α in the presence of CK2β), and UBE2O and PCDL2 (best phosphorylated by phospho- and unmodified CK2α in the presence of CK2β) (Supplementary Figs. 21, 22). Taken together, these results demonstrate that single phosphorylation and O-GlcNAc modifications at sites remote from the active site of a kinase can significantly influence protein substrate selectivity without necessarily modulating kinase activity on short peptides.

Table 2

Protein microarray results for substrate selectivity from CK2α PTM’s

Gene names listed with common protein name in parentheses. See Supplementary Methods for criteria for positive hits.

Form of CK2	α only	α + β
S-GlcNAc	DAPK2 (death-associated protein kinase 2)	AHCYL2 (S-adenosylhomocysteine hydrolase)
Phospho (Pfa)	CPNE1 (copine I isoform a),PGRMC1(progesterone receptor membrane component 1),GOLGA4 (GOLGA4 protein)	NAP1L3 (nucleosome assembly protein1-like 3 or MB20 protein),COL4A3BP (collagen binding protein isoform 2)
Unmodified	MAPK9 (stress activated kinase JNK2),VPS25 (Vacuolar sorting protein 25)	CLGN (calmegin precursor),MLPH (melanophilin),RADP51AP1 (RAD51 associated protein 1)
Both S-GlcNAc & phospho (Pfa)	None	APLP2 (APLP2 protein)
Both S-GlcNAc & unmodified	None	EEF2K (eEF-2 kinase),WASL (Wiskitt-Aldrich syndrome-like protein)SLC7A6OS (Solute carrier protein family7 member 6)
Both Phospho (Pfa) & unmodified	PDCD2L (programmed cell death protein 2-like),EAF2 (ELL associated factor 2),DNAJB2 (DnaJ (Hsp40) homolog B2),PFKM (Phosphofructokinase from muscle)	UBE2O (ubiquitin-conjugating enzyme E2O),HNRNPC (hnRNP C 1/2),MTF2 (Metal-response element-binding transcription factor 2)

Figure 5

Substrate selectivity for CK2

Phosphorimage analysis of in vitro CK2 kinase assays with protein substrates. All reactions were performed at 30 °C. Numbers indicate nM product for each kinase reaction. (a) AHCYL2 substrate (25 ng/µL) with 100 µM ATP and 10 nM CK2α ± 11 nM CK2β for 6 min. (b) NAP1L3 substrate (15 ng/µL) with 100 µM ATP and 10 nM CK2α ± 11 nM CK2β for 6 min. (c) NIPBL substrate (50 ng/µL) with 100 µM ATP and 5 nM CK2α ± 11 nM Pin1 for 5 min. See Supplementary Figs. 19, 25 for full gels corresponding to those in panel a–c.

We performed related protein microarray kinase assays to determine if Pin1 modulates phospho-CK2α activity toward protein substrates. We found no significant differences in kcat or Km values for Pfa344-CK2α with a synthetic peptide substrate in the presence versus the absence of Pin1 (Supplementary Fig. 23), suggesting that this protein-protein interaction does not have a general activity effect on kinase action. However, there are subsets of substrate proteins whose phosphorylation was positively or negatively influenced by Pin1-pThr344-CK2α interaction (Supplementary Table 4, Supplementary Fig. 24). In a solution phase assay with recombinant NIPBL protein substrate, we confirmed that Pin1 dramatically inhibits NIPBL phosphorylation by pThr344-CK2α but has no effect on unmodified CK2α phosphorylation of NIPBL (Fig. 5c and Supplementary Figs. 18b, 24). These results further highlight the combinatorial matrix of PTM-induced effects on CK2α patterns of protein phosphorylation in the proteome.

Discussion

The finding that protein kinase CK2α was posttranslationally modified by O-GlcNAc on a site near a known Cdk-phosphorylation site led us to explore how these modifications may impact CK2 regulation. Expressed protein ligation is a strategy that was well suited for this task, since the modification sites are near the C-terminus of the recombinant protein. We provide evidence that Thr344 phosphorylation and Ser347 O-GlcNAcylation of CK2α transmit reciprocal information important for cell signaling networks. Thr344 phosphorylation enhances the stability of CK2α by Pin1 interaction and can also shape the pattern of protein substrates targeted by CK2. In contrast, it appears that Ser347 O-GlcNAcylation of CK2α may limit its cellular stability by altering Thr344 phosphorylation, and this sugar residue can further induce a distinct pattern of protein substrates phosphorylated by the kinase. Even though we did not see differences in stability between the unmodified and S-GlcNAc-Ser347 CK2α proteins in the microinjection experiments at the time points analyzed, we did observe a modest but reproducible reduction in endogenous CK2α levels when treating with TMG for a longer period. These results may differ since it is presumed that only a minute fraction of the unmodified microinjected protein is phosphorylated in cells during the course of the experiment.

Phosphorylation-dependent interactions with Pin1 have been shown to be stabilizing for other proteins including Nanog[40] and p27Kip1[41]. How Pin1 binding can stabilize CK2 from proteasome-mediated destruction is not yet settled, although one possible mechanism is that the Pin1 complex prevents ubiquitination by sequestration from a requisite E3 ligase[42]. A consequence of our findings is that CK2α levels can spike in cells during the period of mitosis, which might lead to a special set of phosphorylation events. In addition, the function of the different patterns of substrate phosphorylation conferred by Cdk-mediated modification of CK2α and Pin1 interaction might have important roles in mitotic regulation.

The ability of pThr344 and S-GlcNAc347 to influence changes in phosphorylation by CK2 via direct contacts with the purified protein substrates summarized in Table 2 is a noteworthy finding. PTM regulation of the function of kinases is typically associated with general activation or inhibition of a kinase, or to serve as a specific recruiting site for phosphoprotein binding adaptor molecules like SH2 domain or 14-3-3 domain containing proteins. Such specific PTM binding domains are not readily apparent in the CK2 substrates in Table 2, so the mechanism for specificity will be an interesting structural biology challenge for future studies. The implications of the particular CK2 substrate interactions that we identified in Table 2 and Supplementary Table 4 suggest a wide range of biologically processes being affected. For example, CK2 catalyzed phosphorylation of eEF2 kinase and WASL (N-WASP), inhibited by CK2 phosphorylation on Thr344, could influence translation[43] and cytoskeletal dynamics[44,45], respectively. In contrast, pThr344-CK2 is more active as a kinase toward histone chaperone NAP1L3, which could modulate chromatin dynamics[46]. The reversible kinetics of CK2 PTMs in vivo, not captured here using fixed forms of CK2s in the microarray studies, could indeed create a mosaic of complex cellular effects on the proteome.

The marrying of expressed protein ligation to generate site-specific and stoichiometrically modified forms of a protein kinase with protein microarray phosphorylation assays, performed here for the first time, can help illuminate distinct connections in signaling cascades that would be very difficult to discern using other biochemical approaches. While mass-spectrometric based phosphoproteomics[47] using inhibitors or chemical complementation[48] in cellular assays is powerful, it cannot readily provide insights into the substrate-altering behavior of specific PTMs on a kinase. As shown in our study, the common mutagenesis phospho mimic approach, Thr to Glu, fails to replicate the properties of pThr344 in CK2α in Pin1 interaction or in selective phosphorylation of NAP1L3. Moreover, there is no natural amino acid residue that can even be considered a plausible mimic of an O-GlcNAc moiety.

In summary, the complex regulation of CK2 by competing phosphorylation and O-GlcNAcylation provides a new framework for understanding this key signaling enzyme. This study also provides a comprehensive approach to investigating how protein PTMs can mediate multiple actions in a cellular network.

Methods

As described in more detail below and in Supplementary Methods, we used the phospho-mimic Pfa containing protein in all cell microinjection studies. In the Pin1 pull-down assays, we used both the Pfa and pThr containing proteins to demonstrate the ability of Pfa to mimic pThr. To examine and validate protein substrate selectivity influenced by phosphorylation at Thr344, we initially used Pfa, but subsequently validated the results using the natural pThr residue.

Microinjection and immunocytochemistry

For individual microinjections (performed at rt), semisynthetic HA-CK2α proteins, FLAG-CK2β, and other samples were diluted in microinjection buffer and injected into REF52 cells. Following microinjection, cells were incubated (37°C in 5% CO2 for 1–8 h) or fixed immediately (t=0 h). At least 85 cells were injected for each sample and condition in at least three repeated independent experiments. For the experiments, final sample concentrations in the microinjection capillary were as follows: 0.25 µg/µL CK2α; 0.25 µg/µL CK2α + 0.138 µg/µL CK2β (molar equivalent); 0.25 µg/µL CK2α + 1 µM MG132 (LC Biolabs); or 0.25 µg/µL CK2α + 2 µg/µL IgY. Cells were fixed and permeabilized prior to immunostaining with anti-HA mouse antibody (Covance HA.11 Clone 16B12, 1:4000) and DyLight488-conjugated goat anti-mouse IgG (KPL, 1:950). Imaging was performed using an Olympus BX61 upright fluorescence microscope and FITC filter cube. By using SlideBook5 software, fluorescence intensities of all positive cells were quantified, and the sum was multiplied by the number of positive cells divided by the number of injected cells, giving a relative fluorescence intensity value as the indication of the stability of the microinjected proteins inside the cells. Data are presented as the mean ± SD of at least three separate experiments. These values were then normalized to the sample’s t = 0 time point.

Western blots and IPs

For Cdk inhibitor studies, HeLa cells were treated with 0.1% DMSO (control), 2 µM flavopiridol (SantaCruz), or 3 µM 9-cyanopaullone (SantaCruz) for 18 h and membranes were probed with 1:1000 anti-CK2α (Cell Signaling). For nocodazole studies, HeLa cells were treated with 0.1% DMSO (control) or 100 ng/mL nocodazole (Sigma) for 24 h and membranes were probed with 1:800 anti-CK2α (SC-9030 SantaCruz). For O-GlcNAcase inhibitor studies, HeLa cells were treated with 20 µM TMG (synthesized by custom order by SD ChemMolecules) or 50 µM Tris (control) for 12 h or 16 h and membranes were probed with 1:1000 anti-CK2α (Cell Signaling). For IP-Western, HeLa cells were treated with 20 µM TMG or 50 µM Tris (control) for 12 h. CK2α was immunoprecipitated with 2 µg mouse monoclonal anti-CK2α (Abcam 8E5) and membranes were probed with 1:3000 anti-O-GlcNAc mouse IgM (antigen purified CTD110.6 as previously described[49]) or 1:1000 rabbit anti-CK2α (Cell Signaling).

Pull-downs for Pin1

Pin1 was expressed and purified from E. coli as previously described. Pull-down assays were performed with HA-CK2α proteins (700 nM final) immobilized on Protein G Dynabeads (Invitrogen) using anti-HA mouse monoclonal antibody (Covance). Beads were incubated with anti-CK2 antibody for 15 min at rt and then with various CK2α proteins for 40 min at 4 °C before being washed and incubated with recombinant human Pin1 (0.05 µM) at 4 °C for 20 min. To demonstrate that the presence of anti-Pin1 IgY, but not non-specific IgY, can block the binding interactions between pCK2α and Pin1, pull-down assays were performed after recombinant Pin1 (0.1 µM) was allowed to pre-incubate with IgY (0.03 µg/µL) for 10 min at rt.

For co-immunoprecipitation of Pin1, cell lysates were prepared from REF52 cells using Cell Lytic-M (Sigma) reagent diluted in PBS plus protease inhibitors and spiked with either 2.3 µM Pfa344 CK2α or 2.3 µM unmodified CK2α. Lysates were allowed to incubate with semisynthetic HA-CK2α proteins for 30 min at 4 °C prior to the addition of protein G beads bound to anti-HA antibody (for 2 h at 4°C).

Kinase assays on chips

Kinase assays were performed on human protein microarrays provided by the Protein Microarray Core at the High Throughput Biology Center at Johns Hopkins. Each kinase group was run in duplicate. For the first set of kinase assays on the chips, we examined differences in substrate selectivity for the following kinases: unmodified CK2α alone, unmodified CK2α+β, S-GlcNAc-CK2α alone, S-GlcNAc-CK2α+β, Pfa-CK2α alone, Pfa-CK2α+β. Kinase reaction conditions for this set of assays were 50 mM Hepes pH 7.5, 80 mM NaCl, 10 mM MgCl2, 1 mM DTT, 0.1% NP-40, 100 µM ATP, 6 µCi [33P]γ-ATP, with 20 nM CK2α ± 24 nM CK2β (Supplementary Fig. 17). For the second set of kinase assays on the chips, we examined differences in substrate selectivity for the following kinases: unmodified CK2α alone, unmodified CK2α + Pin1, pThr-CK2α alone, pThr-CK2α + Pin1. Kinase reaction conditions for this set of assays were the same as above with the addition of 1 mM MnCl2 and with 50 nM CK2α ± 100 nM Pin1 (Supplementary Fig. 24). Since this set of kinase assays was performed subsequent to the first set reported, we added MnCl2 to enhance the signal of the controls used to align the protein chip results. Chips were exposed to film for 4 weeks. The signal intensity of each spot on the microarray chips was quantified and since the distribution of signal intensities of all of the proteins followed a normal distribution, standard deviation of the signal intensity for each protein was used to qualify a protein as a hit or not (see Supplementary Dataset 1 and Supplementary Results for description of file). We used a stringent cutoff of three standard deviation (SD) values and only proteins identified as “positive hits” in both duplicate experiments were qualified as a “substrate” for a given experiment. To be included in Table 2 rows 1–3, the “positive hit” must have been unique for a CK2 enzyme form, that is it could not be positive in either of the duplicate experiments for any of the other CK2 enzyme forms. To be included in Table 2 rows 4–6, the “positive hit” was positive for two CK2 enzyme forms and it could not have been positive in either duplicate experiments for the alternative CK2 enzyme form.