Akt Phosphorylates MstI and Prevents Its Proteolytic Activation, Blocking FOXO3 Phosphorylation and Nuclear Translocation
2007; Elsevier BV; Volume: 282; Issue: 42 Linguagem: Inglês
10.1074/jbc.m704542200
ISSN1083-351X
AutoresSung‐Wuk Jang, Seung-Ju Yang, Shanthi Srinivasan, Keqiang Ye,
Tópico(s)Cell death mechanisms and regulation
ResumoOxidative stress can induce apoptosis through activation of MstI, subsequent phosphorylation of FOXO and nuclear translocation. MstI is a common component of apoptosis initiated by various stresses. MstI kinase activation requires autophosphorylation and proteolytic degradation by caspases. The role of Akt in regulating MstI activity has not been previously examined. Here, we show that MstI is a physiological substrate of Akt. Akt phosphorylation of MstI diminishes its apoptotic cleavage by caspases and prevents its kinase activity on FOXO3. MstI directly binds to Akt, which is regulated Akt kinase activity. Akt phosphorylates MstI on the Thr387 residue and protects MstI from apoptotic cleavage in vitro and in apoptotic cells. Interestingly, Akt phosphorylation of MstI strongly inhibits its kinase activity on FOXO3. The phosphorylation mimetic mutant MST1 T387E blocks H2O2-triggered FOXO3 nuclear translocation and apoptosis. Thus, our findings support that Akt blocks MstI-triggered FOXO3 nuclear translocation by phosphorylating MstI, promoting cell survival. Oxidative stress can induce apoptosis through activation of MstI, subsequent phosphorylation of FOXO and nuclear translocation. MstI is a common component of apoptosis initiated by various stresses. MstI kinase activation requires autophosphorylation and proteolytic degradation by caspases. The role of Akt in regulating MstI activity has not been previously examined. Here, we show that MstI is a physiological substrate of Akt. Akt phosphorylation of MstI diminishes its apoptotic cleavage by caspases and prevents its kinase activity on FOXO3. MstI directly binds to Akt, which is regulated Akt kinase activity. Akt phosphorylates MstI on the Thr387 residue and protects MstI from apoptotic cleavage in vitro and in apoptotic cells. Interestingly, Akt phosphorylation of MstI strongly inhibits its kinase activity on FOXO3. The phosphorylation mimetic mutant MST1 T387E blocks H2O2-triggered FOXO3 nuclear translocation and apoptosis. Thus, our findings support that Akt blocks MstI-triggered FOXO3 nuclear translocation by phosphorylating MstI, promoting cell survival. FOXO 2The abbreviations used are: FOXO, forkhead box O; MstI, mammalian Sterile20-like 1; GST, glutathione S-transferase; HRP, horseradish peroxidase; DAPI, 4′,6-diamidino-2-phenylindole. (forkhead box O; forkhead members of the O class) are transcription factors. FOXO factors mediate cell death by regulating numerous apoptotic genes transcription (1Kops G.J. Burgering B.M. J. Mol. Med. 1999; 77: 656-665Crossref PubMed Scopus (253) Google Scholar, 2Brunet A. Bonni A. Zigmond M.J. Lin M.Z. Juo P. Hu L.S. Anderson M.J. Arden K.C. Blenis J. Greenberg M.E. Cell. 1999; 96: 857-868Abstract Full Text Full Text PDF PubMed Scopus (5454) Google Scholar, 3Biggs 3rd, W.H. Meisenhelder J. Hunter T. Cavenee W.K. Arden K.C. Proc. Natl. Acad. Sci. U. S. A. 1999; 96: 7421-7426Crossref PubMed Scopus (946) Google Scholar). FOXO factors are insulin-sensitive transcription factors with a variety of downstream targets and interacting partners. Insulin-mediated inhibition of FOXO factors is predominantly regulated through a shuttling mechanism that distributes FOXO localization to the cytoplasm, thereby terminating its transcriptional function (4Van Der Heide L.P. Hoekman M.F. Smidt M.P. Biochem. J. 2004; 380: 297-309Crossref PubMed Scopus (560) Google Scholar). FOXO factors contain three highly conserved putative Akt recognition motifs (RXRXX(S/T), where X denotes any residue), two at the N and C termini, respectively, and one located in the forkhead domain. All FOXO proteins require Akt phosphorylation in the N terminus and in the forkhead domain to translocate from the nucleus to the cytoplasm (5Brownawell A.M. Kops G.J. Macara I.G. Burgering B.M. Mol. Cell Biol. 2001; 21: 3534-3546Crossref PubMed Scopus (269) Google Scholar). The two phosphorylated residues are essential components for translocation, as they influence the NLS (nuclear localization sequence) function and the association with 14-3-3 proteins (2Brunet A. Bonni A. Zigmond M.J. Lin M.Z. Juo P. Hu L.S. Anderson M.J. Arden K.C. Blenis J. Greenberg M.E. Cell. 1999; 96: 857-868Abstract Full Text Full Text PDF PubMed Scopus (5454) Google Scholar). Recently, Bonni and co-workers demonstrated that MstI mediates oxidative stress-induced neuronal apoptosis through FOXO factors by phosphorylating FOXO3 on Ser207. This phosphorylation triggers its nuclear translocation and disrupting the association between 14-3-3 and FOXO in the cytoplasm (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar). MstI belongs to class II GC (protein Ser/Thr) kinase (7Creasy C.L. Chernoff J. J. Biol. Chem. 1995; 270: 21695-21700Abstract Full Text Full Text PDF PubMed Scopus (174) Google Scholar), which contains 487 residues and predominantly resides in the cytoplasm. MstI consists of an N-terminal catalytic domain in the Ste20 class, followed by a non-catalytic tail comprising of an autoinhibitory domain and a coiled-coil domain that mediates dimerization (8Creasy C.L. Ambrose D.M. Chernoff J. J. Biol. Chem. 1996; 271: 21049-21053Abstract Full Text Full Text PDF PubMed Scopus (172) Google Scholar). It has been suggested that, physiologically, MstI exists as an autoinhibitory homodimer that is activated after post-translational modification such as phosphorylation and/or cleavage. Although caspase-mediated cleavage removes the C-terminal regulatory domain, which is associated with an increase in MstI activity, there is evidence that caspase-mediated cleavage alone cannot activate MstI and both phosphorylation and proteolysis are necessary to activate fully this enzyme (9Graves J.D. Draves K.E. Gotoh Y. Krebs E.G. Clark E.A. J. Biol. Chem. 2001; 276: 14909-14915Abstract Full Text Full Text PDF PubMed Scopus (136) Google Scholar, 10Lee K.K. Ohyama T. Yajima N. Tsubuki S. Yonehara S. J. Biol. Chem. 2001; 276: 19276-19285Abstract Full Text Full Text PDF PubMed Scopus (173) Google Scholar, 11Glantschnig H. Rodan G.A. Reszka A.A. J. Biol. Chem. 2002; 277: 42987-42996Abstract Full Text Full Text PDF PubMed Scopus (152) Google Scholar). Indeed, Lee et al. (12Lee K.K. Murakawa M. Nishida E. Tsubuki S. Kawashima S. Sakamaki K. Yonehara S. Oncogene. 1998; 16: 3029-3037Crossref PubMed Scopus (120) Google Scholar) purified a 34-kDa protein that was identified as MstI/MstII but did not have kinase activity. Several phosphorylation sites have now been identified in MstI, namely Thr175, Thr177, Thr183, Thr187, Ser327, and Thr387 (9Graves J.D. Draves K.E. Gotoh Y. Krebs E.G. Clark E.A. J. Biol. Chem. 2001; 276: 14909-14915Abstract Full Text Full Text PDF PubMed Scopus (136) Google Scholar, 11Glantschnig H. Rodan G.A. Reszka A.A. J. Biol. Chem. 2002; 277: 42987-42996Abstract Full Text Full Text PDF PubMed Scopus (152) Google Scholar). Of these, Thr183 and Thr187 appear to be essential for kinase activity (11Glantschnig H. Rodan G.A. Reszka A.A. J. Biol. Chem. 2002; 277: 42987-42996Abstract Full Text Full Text PDF PubMed Scopus (152) Google Scholar). It has been proposed before that phosphorylation of MstI on Thr183 and possibly Thr187 is induced by an existing active MstI (11Glantschnig H. Rodan G.A. Reszka A.A. J. Biol. Chem. 2002; 277: 42987-42996Abstract Full Text Full Text PDF PubMed Scopus (152) Google Scholar). Overexpression of MstI alone is sufficient to initiate apoptosis in various cells, which involves activation of SAPK (stress-activated protein kinase)/JNK (13Graves J.D. Gotoh Y. Draves K.E. Ambrose D. Han D.K. Wright M. Chernoff J. Clark E.A. Krebs E.G. EMBO J. 1998; 17: 2224-2234Crossref PubMed Scopus (325) Google Scholar), p53 (14Lin Y. Khokhlatchev A. Figeys D. Avruch J. J. Biol. Chem. 2002; 277: 47991-48001Abstract Full Text Full Text PDF PubMed Scopus (75) Google Scholar), FOXO (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar). MstI cycles rapidly and continuously through the nucleus (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar, 15Ura S. Masuyama N. Graves J.D. Gotoh Y. Proc. Natl. Acad. Sci. U. S. A. 2001; 98: 10148-10153Crossref PubMed Scopus (140) Google Scholar), and associates with DAP-4 (death-associated protein-4) in the nucleus (14Lin Y. Khokhlatchev A. Figeys D. Avruch J. J. Biol. Chem. 2002; 277: 47991-48001Abstract Full Text Full Text PDF PubMed Scopus (75) Google Scholar), where the catalytic fragment generated during apoptosis triggers chromatin condensation (15Ura S. Masuyama N. Graves J.D. Gotoh Y. Proc. Natl. Acad. Sci. U. S. A. 2001; 98: 10148-10153Crossref PubMed Scopus (140) Google Scholar, 16Cheung W.L. Ajiro K. Samejima K. Kloc M. Cheung P. Mizzen C.A. Beeser A. Etkin L.D. Chernoff J. Earnshaw W.C. Allis C.D. Cell. 2003; 113: 507-517Abstract Full Text Full Text PDF PubMed Scopus (399) Google Scholar). MstI potently interacts with both growth inhibitory proteins RASSF1A and NORE1A. Overexpression of RASSF1A increases kinase activity of MstI in intact cells (17Praskova M. Khoklatchev A. Ortiz-Vega S. Avruch J. Biochem. J. 2004; 381: 453-462Crossref PubMed Scopus (284) Google Scholar), and facilitates MstI activation and thereby promotes apoptosis induced by death receptor signaling (18Oh H.J. Lee K.K. Song S.J. Jin M.S. Song M.S. Lee J.H. Im C.R. Lee J.O. Yonehara S. Lim D.S. Cancer Res. 2006; 66: 2562-2569Crossref PubMed Scopus (157) Google Scholar). Interestingly, PP2A treatment up-regulates MstI kinase activity, whereas EGF treatment decreases its kinase activity, suggesting that phosphorylation on the resting MstI negatively modulates its kinase activity. Mitogenic signal might trigger its further phosphorylation, resulting in reduction of its kinase activity (7Creasy C.L. Chernoff J. J. Biol. Chem. 1995; 270: 21695-21700Abstract Full Text Full Text PDF PubMed Scopus (174) Google Scholar). In this study, we demonstrate that Akt binds and phosphorylates MstI, leading to its resistance against apoptotic cleavage and inhibition of its kinase activity on FOXO3. In addition, we show that MstI T387E, an Akt phosphorylation mimetic mutant, blocks FOXO3 nuclear translocation regardless of H2O2 stimulation, preventing apoptosis. In contrast, MstI T387A, a nonphosphorylated mutant, strongly phosphorylates FOXO3 and triggers its nuclear translocation, enhancing cell death. Cells and Reagents—HEK293 cells were maintained in medium A (DMEM with 10% fetal bovine serum and 100 units of penicillin-streptomycin) at 37 °C with 5% CO2 atmosphere in a humidified incubator. EGF was from Roche Applied Sciences. Anti-caspase-3 and anti-tubulin antibodies were from Santa Cruz Biotechnology, Inc. Anti-Myc, anti-phospho-Akt-473, and anti-Akt were from Cell Signaling. Anti-MstI and anti-phospho-MstI antibodies and active Akt protein were from Upstate Biotechnology, Inc. Anti-Foxo3 Ser207 antibody was from Invitrogen. All the chemicals not included above were from Sigma. Cell-free Apoptotic Solution Preparation and MstI Cleavage Assay—The procedures are exactly as described (19Liu X. Kim C.N. Yang J. Jemmerson R. Wang X. Cell. 1996; 86: 147-157Abstract Full Text Full Text PDF PubMed Scopus (4484) Google Scholar). Briefly, the pellets of 293 cells were washed once with ice-cold phosphate-buffered saline and resuspended in 5 vol of buffer A, supplemented with protease inhibitors. After sitting on ice for 15 min, the cells were broken by passing 15 times through a G22 needle. After centrifugation in a microcentrifuge for 5 min at 4 °C, the supernatants were further centrifuged at 105 × g for 30 min in an ultracentrifuge (Beckman). The resulting supernatants were used for in vitro apoptosis assay. The purified activated caspase 3 was added into S-100 extract to initiate caspase cascade. After 1 h of incubation at 37 °C, in vitro transcripted and translated MstI protein, which was treated with or without active Akt, or purified GST-MstI recombinant proteins were introduced and incubated for another hour. The reaction mixture was analyzed by immunoblotting with anti-GST-HRP or autoradiography, respectively. In Vitro Binding Assays—GST fusion proteins were prepared and coupled to glutathione-Sepharose beads. HEK293 cells were transfected with HA-tagged Akt constructs, and the cells were washed once in phosphate-buffered saline, and lysed in 1 ml of lysis buffer A (50 mm Tris, pH 7.4, 40 mm NaCl, 1 mm EDTA, 0.5% Triton X-100, 1.5 mm Na3VO4, 50 mm NaF, 10 mm sodium pyrophosphate, 10 mm sodium β-glycerophosphate, 1 mm phenylmethylsulfonyl fluoride, 5 mg/ml aprotinin, 1 mg/ml leupeptin, 1 mg/ml pepstatin A), and centrifuged for 10 min at 14,000 × g at 4 °C. The cell lysates were incubated with GST protein-conjugated glutathione beads at 4 °C for 3 h. After incubation, the beads were washed three times with 500 μl of lysis buffer each time. The agarose then was resuspended in 30 μl of sample buffer separated by SDS-PAGE followed by immunoblotting analysis. Cytochemical Staining of Apoptotic Cells—MstI-transfected cells were treated with or without 35 μm etoposide for 16 h, followed by incubation with a fluorescent dye MR(DEVD)2 for 1 h. The red cells are considered apoptotic. Morphological changes in the nuclear chromatin of cells undergoing apoptosis were detected by staining with 4,6-diamidino-2-phenylindole (DAPI) as described (20Ye K. Ke Y. Keshava N. Shanks J. Kapp J.A. Tekmal R.R. Petros J. Joshi H.C. Proc. Natl. Acad. Sci. U. S. A. 1998; 95: 1601-1606Crossref PubMed Scopus (324) Google Scholar). Totally, about 500 nuclei were counted under different fields. The Picture was taken on an Olympus IX71 invert fluorescent microscope. In Vitro Kinase Assay—Ectopically expressed MstI were immunoprecipitated with glutathione beads. After extensive washing, the complex was employed in a kinase assay. The precipitated MstI were incubated with 2 μg of histone H2B or FOXO3 in 20 μl of kinase reaction buffer (20 mm Tris, pH 7.5 with 10 mm MgCl2) containing 25 μm ATP and 2.5 μCi of [γ-32P]ATP for 20 min at 30 °C. Reactions were terminated by adding 7 μl of Laemmli's sample buffer and boiling for 5 min. A portion of the sample (15 μl) was separated on a SDS-polyacrylamide gel and autoradiographed or analyzed by PhosphorImage analyzer. Caspase-3 Activity Assay—Caspase-3 activity was measured by means of the CaspACE Assay System Fluorometric kit (Promega Corp., Madison, WI). Cells were initially seeded at a density of 1 × 106 in 10-cm dishes, and transfected with various GST-tagged MstI constructs, followed by 35 μm VP16 treatment for 24 h, caspase-3 activity was measured by the cleavage of the fluorometric substrate Ac-DEVD-AMC according to the manufacturer's instructions. Subcellular Fractionation—Briefly, GST-MstI constructs transfected HEK293 cells (1 × 106 to 5 × 106/ml) were washed once with 1 ml of phosphate-buffered saline and once with 1 ml of lysis buffer (10 mm Hepes, 10 mm KCl, 1.5 mm MgCl2, 0.5 mm phenylmethylsulfonyl fluoride, 10 μg/ml leupeptin, pH 7.9). Cells were lysed by suspending the cell pellet in 20 μl of lysis buffer containing 0.1% Nonidet P-40 for 10 min on ice. To isolate nuclei, the lysates were microcentrifuged for 5 min at 12,000 × g, and the nuclear pellet was washed with lysis buffer without Nonidet P-40. Nuclear proteins were obtained by resuspending the nuclear pellet in 20 μl of extraction buffer (420 mm NaCl, 20 mm Hepes, 1.5 mm MgCl2, 0.2 mm EDTA, 25% glycerol, pH 7.9) for 10 min at 4 °C. The nuclear suspension was microcentrifuged, the pellet was discarded, and the supernatant was diluted in dilution buffer (50 mm KCl, 20 mm Hepes, 0.2 mm EDTA, 20% glycerol, pH 7.9). Akt Phosphorylates MstI on Thr387—In exploring the sequence of MstI, we noticed that amino acids 120, RLRNKTL; 345, TVRVAST; 387, KRRDETM, correspond to a motif that is identified as a consensus Akt phosphorylation element present in numerous Akt substrates (Fig. 1A). We prepared GST-recombinant proteins from three fragments of MstI containing putative phosphorylation domains, and examined the ability to be phosphorylated by Akt through in vitro kinase assays. Fragment (amino acids 300-487) and positive control GSK-β were robustly phosphorylated by active Akt, as manifested by immunoblotting analysis with anti-phospho-Akt substrate antibody, which recognizes the consensus Akt phosphorylation elements R/KXR/KXX(S/T) present in numerous Akt substrates. By contrast, fragments 1-100 and 1-160 and GST alone were not phosphorylated (Fig. 1B, left panel). Similar results were also observed in the presence of [γ-32P]ATP (data not shown). Mutation with T387A but not S345A abolished MstI phosphorylation by active Akt, suggesting that the Thr387 residue can be phosphorylated by Akt in vitro (Fig. 1C, upper panel), fitting with previous report that Thr387 is a phosphorylation site on MstI (11Glantschnig H. Rodan G.A. Reszka A.A. J. Biol. Chem. 2002; 277: 42987-42996Abstract Full Text Full Text PDF PubMed Scopus (152) Google Scholar). To explore whether MstI can be phosphorylated by Akt in intact cells, we transfected HEK293 cells with GST-tagged MstI and pretreated the cells with various inhibitors, followed by EGF stimulation. The transfected GST proteins were pulled down with glutathione beads and monitored by immunoblotting analysis with anti-phospho-Akt substrate antibody. EGF treatment triggered a potent phosphorylation in MstI, which was substantially decreased by PI 3-kinase inhibitor LY294002 and Wortmannin but not PKC inhibitor GF109203X or MEK1 inhibitor PD98059 (Fig. 1D, top panel). Equal amounts of GST fusion proteins were precipitated (Fig. 1D, 2nd panel). Akt phosphorylation status tightly coupled to MstI phosphorylation (3rd panel). Immunoblotting with anti-phospho-MstI Thr387 antibody further confirmed that Akt phosphorylates MstI on Thr387 residue in intact cells (Fig. 1D, bottom panel) To ascertain that MstI is the physiological substrate of Akt, we transfected HEK293 cells with GST-MstI, and infected the transfected cells with adenovirus expressing plasma membrane localized active myristoylated Akt or sh-RNA of Akt. MstI was pulled down with glutathione beads. Immunoblotting analysis reveals that MstI was robustly phosphorylated by Myr-Akt, and its phosphorylation was completely blocked when Akt was depleted (Fig. 1E, top left panel). Mutation of Thr387 into alanine totally abolished MstI phosphorylation by membrane-localized active Akt (Fig. 1E, top right panel). Immunoblotting with anti-phospho-MstI Thr387 antibody verified these observations (Fig. 1E, bottom panels). Endogenous MstI exhibited the similar results (Fig. 1F). Thus, Akt phosphorylates MstI in vitro and in vivo. Akt Associates with MstI—Akt can exist in a stable complex with several of its substrate proteins (e.g. Mdm2, TSC2, EDG-1) and can also interact with many proteins that do not serve as Akt substrate, but rather seem to play a modulatory role in Akt regulation (21Brazil D.P. Park J. Hemmings B.A. Cell. 2002; 111: 293-303Abstract Full Text Full Text PDF PubMed Scopus (488) Google Scholar). To explore whether MstI binds to Akt, we transfected HA-Akt into HEK293 cells with GST-MstI construct, and pretreated the transfected cells with various pharmacological agents, followed by EGF for 10 min. GST-MstI proteins was pulled down with glutathione beads, and the associated proteins were analyzed with anti-HA antibody. MstI potently associated with Akt, and EGF treatment enhanced their binding. PI3-kinase inhibitor wortmannin or LY294002 pretreatment markedly attenuated the association. By contrast, PKC inhibitor GF109203X had no effect (Fig. 2A, top panel). Equal amounts of transfected GST-MstI and HA-Akt proteins and Akt phosphorylation status were verified (Fig. 2A, 2nd, 3rd, and bottom panels). As control, PKC kinase inhibitory effect by GF109203X was verified (Fig. 2A, 4th panel). To determine whether endogenous MstI binds to Akt in HEK293 cells, we conducted coimmunoprecipitation with anti-Akt antibody. Compared with control cells, EGF treatment stimulated robust interaction between MstI and Akt. PI3-kinase inhibitors pretreatment significantly decreased the binding; by contrast, PKC inhibitor exhibited negligible effect (Fig. 2B, top panel). Akt phosphorylation was robustly blocked by PI 3-kinase inhibitors (Fig. 2B, 2nd panel). As the control, PKC kinase inhibitory effect by GF109203X was verified (Fig. 2B, 3rd panel). Similar levels of total protein lysate were employed in all samples, and equal amounts of MstI was pulled-down (Fig. 2B, 4th, 5th, and bottom panels). Thus, activation of PI 3-kinase pathway is indispensable for the interaction between Akt and MstI. To further explore the interaction between Akt and MstI, we transfected HA-Akt into HEK293 cells with various GST-tagged MstI constructs. GST pull-down assay demonstrates that Akt robustly interacted with various MstI proteins except T387A, a mutant unable to be phosphorylated by Akt (Fig. 2C). These results suggest that MstI phosphorylation by Akt is essential for its association with Akt. Nevertheless, MstI phosphorylation on Thr183 or its kinase activity is not required for its interaction with Akt. To explore whether Akt kinase activity is also implicated in this event, we conducted coimmunoprecipitation studies with a variety of Akt constructs. MstI strongly bound to both wild-type and constitutively active Akt-CA (T308DS473D), but it failed to interact with kinase-dead Akt-KD (K179M) or phosphorylation mimetic Akt lacking kinase activity Akt-KD* (T308DS473DK179M) (Fig. 2D). These results indicate that Akt phosphorylation status is not imperative for its association with MstI; instead, its kinase activity is critical for this event. Mapping assay with a variety of MstI fragments reveals that the C terminus of MstI was strongly involved in binding to Akt (Fig. 2E). Therefore, Akt interacts with MstI, for which Akt kinase activity is indispensable. Akt Phosphorylation of MstI Prevents Its Proteolytic Cleavage and Blocks Apoptosis—MstI undergoes several proteolytic cleavage during apoptosis (10Lee K.K. Ohyama T. Yajima N. Tsubuki S. Yonehara S. J. Biol. Chem. 2001; 276: 19276-19285Abstract Full Text Full Text PDF PubMed Scopus (173) Google Scholar, 13Graves J.D. Gotoh Y. Draves K.E. Ambrose D. Han D.K. Wright M. Chernoff J. Clark E.A. Krebs E.G. EMBO J. 1998; 17: 2224-2234Crossref PubMed Scopus (325) Google Scholar). MstI can be cleaved at DEMD326 and TMTD349 to generate catalytically active enzyme of 36 and 40 kDa, respectively. To examine whether Akt phosphorylation could suppress its degradation by caspases, we radiolabeled wild-type and T387A mutant MstI with [35S]methionine. After incubation with active Akt, the reaction mixture was introduced into active cell-free apoptotic solution, consisting of HEK293 cell cytosol supplemented with purified active caspase 3 (19Liu X. Kim C.N. Yang J. Jemmerson R. Wang X. Cell. 1996; 86: 147-157Abstract Full Text Full Text PDF PubMed Scopus (4484) Google Scholar). Autoradiography shows that wild-type MstI was completely cleaved in active S-100, yielding 37- and 25-kDa fragments, which was completely blocked by caspase inhibitor (Fig. 3A, lanes 2 and 4). Akt phosphorylation evidently reduced its proteolytic degradation, leading to a portion of full-length MstI remained intact. In contrast, MstI T387A mutant was actively cleaved irrespective of Akt treatment, as equal amounts of 37- and 25-kDa cleaved products presented in both samples (Fig. 3A, lanes 6 and 7), suggesting that Akt phosphorylation of MstI protects it from apoptotic degradation. The phosphorylation of MstI was verified by anti-phospho-MstI Thr387 antibody (data not shown). To compare whether different MstI mutants possess distinct apoptotic cleavage activities, we prepared numerous GST-MstI recombinant proteins and incubated with active cell-free apoptotic solution. Immunoblotting analysis reveals that T387A was completely degraded and T183E cleavage was faster than wild-type MstI. Nonetheless, T387E exhibited the slowest degradation rate, indicating that Akt phosphorylation protects it from caspase cleavage. These data suggest that Thr183 phosphorylation enhances MstI apoptotic cleavage, and blockade of MstI phosphorylation by Akt evidently facilitates its apoptotic cleavage (Fig. 3B). To investigate whether Akt phosphorylation of MstI protects it from proteolytic degradation in apoptotic cells, we transfected HEK293 cells with various MstI constructs and treated the transfected cells with VP16. Wild-type MstI and kinase-dead K59R mutant were actively cleaved upon VP16 treatment. Interestingly, T183A was evidently cut regardless of VP16 stimulation. Notably, T387E, which mimics Akt phosphorylation, somehow resisted against apoptotic cleavage compared with other constructs (Fig. 3C). Apoptotic assay with a fluorescent dye MR(DEVD)2, which turns red upon caspase-3 cleavage, showed that transfection of T387A alone initiated the most apoptosis, followed by T183E. However, kinase-dead MstI (K59R), wild-type MstI, and T183A displayed similar apoptotic activities. The lowest apoptosis occurs to Akt phosphorylation mimetic mutant T387E. VP16 treatment virtually displayed the similar apoptotic activity pattern with the most apoptosis in T387A cells and the least cell death in T387E (Fig. 3D, left panel). Caspase-3 activity assay revealed the parallel effects (Fig. 3D, right panel). Therefore, our data support that Akt phosphorylates MstI, protects MstI from apoptotic degradation and suppresses the programmed cell death. Akt Phosphorylation of MstI Inhibits Its Kinase Activity on FOXO3—Previous studies demonstrate that histone H2B and FOXO3 are the substrates of MstI (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar, 16Cheung W.L. Ajiro K. Samejima K. Kloc M. Cheung P. Mizzen C.A. Beeser A. Etkin L.D. Chernoff J. Earnshaw W.C. Allis C.D. Cell. 2003; 113: 507-517Abstract Full Text Full Text PDF PubMed Scopus (399) Google Scholar). Histone H2BS14 is reported to be directly phosphorylated by MstI during apoptosis to trigger chromatin condensation (16Cheung W.L. Ajiro K. Samejima K. Kloc M. Cheung P. Mizzen C.A. Beeser A. Etkin L.D. Chernoff J. Earnshaw W.C. Allis C.D. Cell. 2003; 113: 507-517Abstract Full Text Full Text PDF PubMed Scopus (399) Google Scholar). To explore the effect of Akt phosphorylation on MstI kinase activity, we conducted in vitro kinase assay with various MstI recombinant proteins using H2B as a substrate. As expected, both wild-type and MstI T183E mutant potently phosphorylated H2B, whereas MstI T183A exhibited a decreased activity. The kinase-dead MstI K59R failed to phosphorylate H2B. Surprisingly, MstI T387E, an Akt phosphorylation mimetic mutant, displayed the strongest kinase activity on H2B, while its unphosphorylated mutant T387A was unable to phosphorylate H2B (Fig. 4A). These results suggest that Akt phosphorylation of MstI enhances its kinase activity on H2B. However, when we performed MstI kinase assay with FOXO3 as a substrate, we found that MstI T183E exhibited a kinase activity much less than that of wild-type or T183A MstI. Interestingly, MstI T387A robustly phosphorylated FOXO3. By contrast, both MstI K59R and T387E failed to phosphorylate FOXO3 (Fig. 4B, left panel). MstI phosphorylates FOXO3 on Ser207 and triggers its nuclear translocation (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar). To confirm the specificity of FOXO3 phosphorylation by MstI, we conducted MstI kinase assay with S207A FOXO3 recombinant protein as a substrate. None of MstI proteins was able to phosphorylate the mutant (Fig. 4B, right panel), verifying that Ser207 is the MstI phosphorylation site and our kinase assay for FOXO3 is specific. Quantitative analysis showed that MstI T387A and T387E mutants exhibited the completely opposite kinase activities on H2B and FOXO3. Interestingly, MstI T183A and T183E possessed inverse kinase activities on H2B and FOXO3 as well (Fig. 4C). To further examine the effect of H2B and FOXO3 phosphorylation by various MstI mutants, we performed immunoblotting analysis with MstI-transfected cells. Compared with the pronounced kinase activities by other MstI proteins, neither MstI T387A nor MstI K59R was able to trigger H2BS14 phosphorylation in the transfected cells (Fig. 4D, top panel), consistent with the in vitro kinase assay results. Interestingly, both wild-type MstI and T387A mutant strongly phosphorylated FOXO3, whereas MstI T387E and MstI K59R mutants failed to phosphorylate FOXO3 in the transfected cells, fitting with the in vitro findings. Similarly, MstI T187A displayed slightly higher kinase activity on FOXO3 than MstI T183E did (Fig. 4D, 2nd panel). As expected, we did not observe any phosphorylation on FOXO3 S207A mutant (Fig. 4E). To further confirm the notion that blocking Akt phosphorylation on MstI enhances its kinase activity on FOXO3, we treated HEK293 cells with various pharmacological inhibitors and monitored FOXO3 Ser207 and H2BS14 phosphorylation. EGF suppressed FOXO3 Ser207 phosphorylation, and inhibition of Akt activation by PI 3-kinase inhibitors lead to marked phosphorylation of FOXO3 Ser207. By contrast, the PKC inhibitor GF109203X had no effect. Nevertheless, H2BS14 phosphorylation was not affected by any of the above treatments (Fig. 4F). Thus, these data demonstrate that blockage of Akt activity strongly promotes MstI kinase activity on FOXO3, but it has no effect on H2B. To investigate whether MstI apoptotic cleavage is required for Akt-mediated mechanism, we employed MstI D326N and D330N mutants, which resist against proteolytic cleavage by caspases. Compared with potent Ser207 phosphorylation in FOXO3 by wild-type MstI, both MstI D326N and D330N mutants barely phosphorylated FOXO3. Ablation of endogenous Akt enhanced MstI kinase activity on FOXO3, which was substantially attenuated by overexpression of active Akt-CA. The apoptotic cleavage-resistant MstI mutants displayed negligible kinase activity on FOXO3 regardless of Akt (Fig. 4G, top panel). By contrast, H2BS14 was not obviously altered no matter which MstI construct was transfected, and Akt protein level had no significant affect either (Fig. 4G, 3rd panel). Hence, MstI apoptotic cleavage is required for Akt to exert its regulatory effect on MstI kinase activity to FOXO3 but not to H2B. Akt Phosphorylation Mimetic MstI T387E Prevents H2O2-triggered FOXO3 Nuclear Translocation—Upon oxidative stress, MstI phosphorylates FOXO3 on Ser207 and triggers its nuclear translocation and induces neuronal cell death (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar). To explore the physiological consequence of Akt phosphorylation of MstI, we monitored FOXO3 nuclear translocation in cotransfected HEK293 cells in the presence or absence of H2O2 stimulation. In the absence of H2O2, a portion of FOXO3 (18%) resided in the nucleus when cotransfected with wild-type MstI and 74% of FOXO3 translocated into the nucleus in T183E-cotransfected cells. Interestingly, 88% of FOXO3 occurred in the nucleus when cotransfected with T387A. Negligible nuclear FOXO3 was found when cotransfected with T187A, T387E, or K59R. In response to H2O2 treatment, 78% FOXO3 distributed in the nucleus when cotransfected with wild-type MstI, and the ratios increased to 93 and 97% in T183E and T387A cotransfected cells. By contrast, ∼20% nuclear FOXO3 occurred when cotransfected with T387E or K59R. T183A evidently triggered FOXO3 phosphorylation, it also strongly provoked FOXO3 nuclear translocation upon H2O2 stimulation (Fig. 5, A and B). The quantitative analysis is summarized in Fig. 5C. Thus, these data demonstrate that Akt phosphorylation of MstI prevents FOXO3 nuclear translocation. Inhibition of MstI phosphorylation by Akt enhances FOXO3 nuclear residency. To further test the notion the blockage of MstI phosphorylation by Akt elicits FOXO3 nuclear residency, we transfected HEK293 cells with FOXO3, and infected the transfected cells with control adenovirus or virus expressing shRNA-Akt, followed by H2O2 stimulation. We monitored FOXO3 nuclear translocation by immunostaining. In the absence of H2O2, 11% of FOXO3 is in the control nucleus. Depletion of Akt enhanced the ratios to 38%. H2O2 stimulation triggered 79% FOXO3 nuclear translocation, which was further elevated to 98% when Akt was knocked down (Fig. 5D), underscoring that inhibition of MstI phosphorylation by depletion of Akt increased FOXO3 nuclear retention. These results are consistent with the observations in MstI T387A transfected cells. As an alternative approach to explore the effect of MstI phosphorylation by Akt on FOXO3 nuclear translocation, we conducted subcellular fractionation assay with various GST-MstI constructs transfected HEK293 cells. In the nuclear fraction, p-FOXO3 was markedly increased upon H2O2 treatment in most of GST-MstI construct-transfected cells except MstI T387E (Fig. 5E, top panel), an effect correlating with the quantitative nuclear translocation results. The minor ratio discrepancy between wild-type and T183A MstI in nuclear fractionation and microscopic examination might be due to the variation from the different analytical approaches. The purity of nuclear fraction was verified by immunoblotting with anti-tubulin and anti-PARP antibodies, respectively (Fig. 5E, middle and bottom panels). Thus, Akt phosphorylates MstI and inhibits its kinase activity on FOXO3, preventing FOXO3 nuclear translocation. In this study, we have demonstrated that MstI acts as a physiological substrate of Akt. Akt phosphorylation of MstI protects MstI from apoptotic cleavage. Interestingly, this phosphorylation substantially enhances its in vitro kinase activity to H2B and completely abolishes its kinase activity to FOXO3. Moreover, we provide compelling evidence that Akt mediates MstI kinase activity on FOXO3 Ser207 but not on H2BS14 in intact cells. Thus, these data support that MstI possesses distinct effects on FOXO3 and histone H2B, although both nuclear proteins are implicated in apoptosis. David Allis and co-workers (16Cheung W.L. Ajiro K. Samejima K. Kloc M. Cheung P. Mizzen C.A. Beeser A. Etkin L.D. Chernoff J. Earnshaw W.C. Allis C.D. Cell. 2003; 113: 507-517Abstract Full Text Full Text PDF PubMed Scopus (399) Google Scholar) show that MstI can phosphorylate H2B at Ser14 in vitro and in vivo, and the onset of H2BS14 phosphorylation is dependent upon cleavage of MstI by caspase-3. Moreover, H2BS14 phosphorylation correlates with apoptotic chromatin condensation, indicating that MstI phosphorylates H2BS14 and promotes apoptotic chromatin condensation. Surprisingly, MstI T387E, an Akt phosphorylation mimetic mutant, exhibits the strongest kinase activity on H2B, a nonspecific universal substrate for in vitro kinase assay. However, T387A fails to phosphorylate H2B, acting exactly as kinase-dead K59R in vitro and in transfected cells (Fig. 4, A and D). This observation suggests that MstI Thr387 phosphorylation by Akt is necessary for the phosphorylation of H2BS14. If H2B is a physiological substrate of MstI as claimed by Allis group, then Akt phosphorylation of MstI should decrease its kinase activity on H2BS14 to repress apoptosis, which is completely opposite to our results in Fig. 4, A and D. Hence, our finding does not support the previous report that MstI is a physiological kinase for H2B. Our discovery is supported by a recent report that H2BS14 phosphorylation is almost negligible in PKC-δ-deficient B cells compared with wild-type cells and PKC-δ but not MstI might be responsible for H2BS14 phosphorylation in apoptotic cells (22Blois J.T. Mataraza J.M. Mecklenbrauker I. Tarakhovsky A. Chiles T.C. J. Biol. Chem. 2004; 279: 30123-30132Abstract Full Text Full Text PDF PubMed Scopus (37) Google Scholar). Conceivably, MstI might regulate PKC-δ kinase activity on H2BS14 phosphorylation during apoptosis. On the other hand, we observed marked FOXO3 Ser207 phosphorylation in vitro and in transfected cells by T387A but not T387E, indicating that MstI phosphorylation by Akt blocks its kinase activity on FOXO3. This finding fits perfectly with the current paradigm that Akt promotes cell survival by phosphorylating and inhibiting pro-apoptotic proteins. Akt phosphorylates FOXO3 and elicits its cytoplasmic translocation and association with 14-3-3, preventing its transcriptional activity (2Brunet A. Bonni A. Zigmond M.J. Lin M.Z. Juo P. Hu L.S. Anderson M.J. Arden K.C. Blenis J. Greenberg M.E. Cell. 1999; 96: 857-868Abstract Full Text Full Text PDF PubMed Scopus (5454) Google Scholar). Recently, MstI has been reported to act oppositely. Oxidative stress triggers MstI to phosphorylate FOXO3 and promotes its nuclear translocation and dissociates from 14-3-3, enhancing neuronal apoptosis (6Lehtinen M.K. Yuan Z. Boag P.R. Yang Y. Villen J. Becker E.B. DiBacco S. de la Iglesia N. Gygi S. Blackwell T.K. Bonni A. Cell. 2006; 125: 987-1001Abstract Full Text Full Text PDF PubMed Scopus (665) Google Scholar). Here, we show that Akt physically associates with MstI and phosphorylates it and abolishes its kinase activity on FOXO3, resulting in FOXO3 cytoplasmic retention (Fig. 5). Further, we show that T387A, a nonphosphorylated MstI mutant, possesses robust kinase activity on FOXO3 and elicits its nuclear distribution even in the absence of oxidative stress. Both gain-of-function and loss-of-function experiments support that Akt mediates FOXO3 nuclear export not only through direct modification of FOXO3 by Akt but also through phosphorylation of MstI to block its stimulatory effect on FOXO3 nuclear translocation. Accumulative evidence supports that Akt suppresses apoptosis through phosphorylating and inhibiting pro-apoptotic effectors including Bad (23Datta S.R. Dudek H. Tao X. Masters S. Fu H. Gotoh Y. Greenberg M.E. Cell. 1997; 91: 231-241Abstract Full Text Full Text PDF PubMed Scopus (4957) Google Scholar, 24del Peso L. Gonzalez-Garcia M. Page C. Herrera R. Nunez G. Science. 1997; 278: 687-689Crossref PubMed Scopus (1989) Google Scholar), caspase-9 (25Cardone M.H. Roy N. Stennicke H.R. Salvesen G.S. Franke T.F. Stanbridge E. Frisch S. Reed J.C. Science. 1998; 282: 1318-1321Crossref PubMed Scopus (2735) Google Scholar), and acinus (26Hu Y. Yao J. Liu Z. Liu X. Fu H. Ye K. EMBO J. 2005; 24: 3543-3554Crossref PubMed Scopus (75) Google Scholar) etc. Here, we provide more evidence that Akt promotes cell survival by phosphorylating and inhibiting the apoptotic kinase MstI. MstI acting as an apoptotic kinase requires both caspase cleavage and phosphorylation (11Glantschnig H. Rodan G.A. Reszka A.A. J. Biol. Chem. 2002; 277: 42987-42996Abstract Full Text Full Text PDF PubMed Scopus (152) Google Scholar, 27de Souza P.M. Lindsay M.A. Biochem. Soc. Trans. 2004; 32: 485-488Crossref PubMed Scopus (52) Google Scholar). Interestingly, MstI may function both upstream and downstream of caspases, because exogenously expressed MstI activates caspases, which results in its own cleavage (13Graves J.D. Gotoh Y. Draves K.E. Ambrose D. Han D.K. Wright M. Chernoff J. Clark E.A. Krebs E.G. EMBO J. 1998; 17: 2224-2234Crossref PubMed Scopus (325) Google Scholar). In the current study, we show that Akt phosphorylates MstI and protects it from apoptotic process (Fig. 3). Although Akt directly binds MstI, which might shield MstI from proteolytic attack; however, we show that T387E, a phosphorylation mimetic mutant, resists against caspase-mediated cleavage, whereas T387A, a nonphosphorylated mutant, displays the fastest degradation effect. These results support that Akt protects MstI through phosphorylation on Thr387 residue. Recently, it has been report that MstI and RanBP2 levels are elevated in transgenic animals that express a constitutively active p110-α subunit in the epithelial cells of the prostate. Additionally, Akt phosphorylation, MstI and RanBP2 protein levels, can be inhibited in transgenic animals by LY294002 (28Renner, O., Fominaya, J., Alonso, S., Blanco-Aparicio, C., Leal, J. F., and Carnero, A. (2007) Carcinogenesis, 28, 1418-1425Google Scholar). This finding is consistent with our conclusion that Akt phosphorylation of MstI protects it from apoptotic degradation. Taken together, our findings demonstrate that MstI is a physiological substrate of Akt. In addition to direct phosphorylation of FOXOs, Akt exerts its anti-apoptotic action on FOXOs by phosphorylation of MstI and blockage of its kinase activity. We thank Dr. Alfred Reszka at Merck Research Laboratories, West Point, PA for providing various MstI plasmids.
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