Degradation of Tiam1 by Casein Kinase 1 and the SCFβTrCP Ubiquitin Ligase Controls the Duration of mTOR-S6K Signaling*

Background: The guanine nucleotide exchange factor Tiam1 regulates the activity of the small GTPase Rac1, a crucial regulator of cell adhesion, proliferation, and survival. Results: The SCFβTrCP ubiquitin ligase in cooperation with CK1 targets Tiam1 for proteasome-dependent degradation. Conclusion: Tiam1 degradation is required to terminate the mTOR-S6K signaling pathway. Significance: Tiam1 degradation controls the duration of mTOR-S6K signaling in response to mitogens. Tiam1 (T-cell lymphoma invasion and metastasis 1) is a guanine nucleotide exchange factor that specifically controls the activity of the small GTPase Rac, a key regulator of cell adhesion, proliferation, and survival. Here, we report that in response to mitogens, Tiam1 is degraded by the ubiquitin-proteasome system via the SCFβTrCP ubiquitin ligase. Mitogenic stimulation triggers the binding of Tiam1 to the F-box protein βTrCP via its degron sequence and subsequent Tiam1 ubiquitylation and proteasomal degradation. The proteolysis of Tiam1 is prevented by βTrCP silencing, inhibition of CK1 and MEK, or mutation of the Tiam1 degron site. Expression of a stable Tiam1 mutant that is unable to interact with βTrCP results in sustained activation of the mTOR/S6K signaling and increased apoptotic cell death. We propose that the SCFβTrCP-mediated degradation of Tiam1 controls the duration of the mTOR-S6K signaling pathway in response to mitogenic stimuli.


Tiam1 (T-cell lymphoma invasion and metastasis 1) is a gua-
nine nucleotide exchange factor that specifically controls the activity of the small GTPase Rac, a key regulator of cell adhesion, proliferation, and survival. Here, we report that in response to mitogens, Tiam1 is degraded by the ubiquitin-proteasome system via the SCF ␤TrCP ubiquitin ligase. Mitogenic stimulation triggers the binding of Tiam1 to the F-box protein ␤TrCP via its degron sequence and subsequent Tiam1 ubiquitylation and proteasomal degradation. The proteolysis of Tiam1 is prevented by ␤TrCP silencing, inhibition of CK1 and MEK, or mutation of the Tiam1 degron site. Expression of a stable Tiam1 mutant that is unable to interact with ␤TrCP results in sustained activation of the mTOR/S6K signaling and increased apoptotic cell death. We propose that the SCF ␤TrCP -mediated degradation of Tiam1 controls the duration of the mTOR-S6K signaling pathway in response to mitogenic stimuli.
Tiam1 is a ubiquitously expressed guanine nucleotide exchange factor that specifically activates the Rho-like GTPase Rac1 in response to growth factors and cell-substrate interaction (1)(2)(3). It was originally identified in a retroviral insertional mutagenesis screen for genes that confer invasive properties to T-lymphoma cells (1). Thereafter, a plethora of studies have demonstrated that Tiam1 controls different Rac-dependent cellular processes, such as cell polarity, cell-matrix adhesion, cell-cell adhesion, cell survival, and cell growth and proliferation. Hence, it does not come as a surprise that Tiam1 plays a critical role in cancer development. Tiam1 deficiency in mice protects against Ras-induced skin carcinogenesis and correlates with increased apoptosis and reduced proliferation and growth in keratinocytes (4). This is in agreement with in vitro studies reporting that Tiam1 associates with GTP-bound Ras through a Ras-binding domain and functions as an effector that mediates Ras activation of Rac (4). However, the fewer skin tumors developing in Tiam1 knock-out mice progress more frequently to malignancy, indicating that loss of Tiam1 stimulates malignant conversion (4). Indeed, in vitro, Tiam1 is known to promote the formation of adherens junctions and the induction of an epithelial-like phenotype in mesenchymal cells (5,6) and to be required for both the formation and maintenance of cadherin-based adhesions (7).
Despite the importance of Tiam1 in cancer, little is known about the regulation of Tiam1 protein levels in normal and cancer cells. Here, we report that in response to mitogenic stimulation, Tiam1 is targeted for proteasome-dependent degradation by the SCF ␤TrCP ubiquitin ligase in cooperation with casein kinase 1 and the MEK/ERK pathway. We also show that ubiquitin-dependent degradation of Tiam1 is required to terminate the activation of mTOR-S6K signaling in response to mitogenic stimulation.
Purification of ␤TrCP2 Interactors-HEK293T cells grown in 15-cm dishes were transfected with pcDNA3-2ϫFLAG-2ϫHA-␤TrCP2 and treated with 10 M MG132 for 5 h. Cells were harvested and subsequently lysed in lysis buffer (50 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1 mM EDTA, 0.5% Nonidet P-40, 2 mM ␤-glycerophosphate plus protease and phosphatase inhibitors). ␤TrCP2 was immunopurified with mouse anti-FLAG M2-agarose resin (Sigma-Aldrich). After washing, proteins were eluted by competition with FLAG peptide (Sigma-Aldrich). The eluate was then subjected to a second immunopurification with anti-HA resin (12CA5 monoclonal antibody cross-linked to protein G-Sepharose; Invitrogen) prior to elution in Laemmli sample buffer. The final eluate was separated by SDS-PAGE, and proteins were visualized by colloidal Coomassie Blue. Bands were sliced out from the gels and subjected to in-gel digestion. Gel pieces were then reduced, alkylated, and digested according to a published protocol (9). For mass spectrometric analysis, peptides recovered from in-gel digestion were separated with a C18 column and introduced by nanoelectrospray into the LTQ Orbitrap XL (Thermo Fisher) with a configuration as described (10). Peak lists were generated from the MS/MS spectra using MaxQuant build 1.0.13.13 and then searched against the IPI Human database (version 3.37, 69164 entries) using Mascot search engine (Matrix Science). Carbaminomethylation (ϩ57 Da) was set as fixed modification and protein N-terminal acetylation and methionine oxidation as variable modifications. Peptide tolerance was set to 7 ppm, and fragment ion tolerance was set to 0.5 Da, allowing two missed cleavages with trypsin enzyme. Finally, Scaffold (version Scaf-fold_3.6.1; Proteome Software Inc.) was used to validate MS/MS-based peptide and protein identifications. Peptide identifications were accepted if their Mascot scores exceeded 20.
Gene Silencing by Small Interfering RNA-The oligonucleotides designed for targeting both ␤TrCP1 and ␤TrCP2 are as follows: sense sequence, 5Ј-GTGGAATTTGTGGAACATC dTdT-3Ј; and antisense sequence, 5Ј-GATGTTCCACAAAT-TCCACdTdT-3Ј. Cells were transfected with the oligonucleotides twice (24 and 48 h after plating) using Oligofectamine (Invitrogen) according to the manufacturer's recommendations. Forty-eight hours after the last transfection, lysates were prepared and analyzed by immunoblotting.
Phosphorylation Analysis by Mass Spectrometry-Samples were reduced with 10 mM DTT for 30 min at 60°C, followed by 30-min incubation with iodoacetamide (20 mM) in the dark at room temperature. The first digestion was performed using Lys-C for 4 h at 37°C. Subsequently, the digest was diluted 5-fold using 50 mM ammonium bicarbonate to a final urea concentration of less than 2 M, and a second digestion with trypsin was performed overnight at 37°C. Finally, the digestion was quenched by the addition of formic acid to a final concentration of 0.1% (v/v). The resulting solution was desalted using 200-mg Sep-Pak C18 cartridges (Waters Corporation), lyophilized, and reconstituted in 10% formic acid. LC-MSMS was performed with higher energy collision dissociated in a Q-Exactive Plus Orbitrap instrument. MS spectra to peptide sequence assignment were performed with Proteome Discoverer version 1.4 and MASCOT version 2.4 as search engine. The localization of phosphorylated sites was evaluated with PhosphoRS version 3 (11).
Rac Activity Assay-The abundance of GTP-bound Rac1 was determined as follows. Cells were lysed in lysis buffer (10 mM Tris, 150 mM NaCl, 50 mM MgCl 2 , 0.5% Nonidet P-40) containing 2 g of biotinylated p21-binding domain of Pak1. The cleared supernatant was then incubated with streptavidin beads for 30 min at 4°C. Beads were washed, and GTP-bound Rac1 was analyzed by immunoblotting with an anti-Rac1 antibody (Upstate Biotechnology Inc.).

RESULTS
Tiam1 Interacts with ␤TrCP-In an attempt to identify new targets of the SCF ␤TrCP ubiquitin ligase, we expressed ␤TrCP with an N-terminal FLAG-HA epitope tag in HEK293T cells and purified FLAG-HA-␤TrCP immunoprecipitates, which were then analyzed by mass spectrometry. In two independent immunopurifications, peptides corresponding to Tiam1 (T-cell lymphoma invasion and metastasis 1) were recovered (Fig. 1A). Conversely, when we immunopurified Tiam1 from HEK293T cells, we identified peptides corresponding to ␤TrCP (Fig. 1B). To confirm the binding between ␤TrCP and Tiam1 and test its specificity, we overexpressed different FLAG-tagged F-box proteins (all containing WD40 repeats) in HEK293T cells. We then carried out FLAG immunoprecipitations to examine the interaction with endogenous Tiam1. ␤TrCP1 and its paralog ␤TrCP2 were the only proteins able to coimmunoprecipitate with Tiam1 (Fig. 1C). The coimmunoprecipitation of endogenous ␤TrCP with exogenously expressed Tiam1 was confirmed by immunoprecipitation coupled to immunoblotting (Fig. 1D).
It has been shown that substitution to alanine of Arg 474 in ␤TrCP1 (or Arg 447 in ␤TrCP2) within its WD40 ␤-propeller structure disrupts ␤TrCP interaction with the substrate (8,12). To assess whether the interaction between Tiam1 and ␤TrCP is mediated by the ␤TrCP WD40 ␤-propeller, we immunoprecipitated FLAG-tagged wild type ␤TrCP2 and the ␤TrCP2(R447A) mutant from HEK293T cells and examined their binding to endogenous Tiam1. As shown in Fig. Forty-eight hours after transfection, cells were treated for 5 h with the proteasome inhibitors MG132, then harvested, and lysed. Whole cell extracts (WCE) were immunoprecipitated (IP) with anti-FLAG antibody and immunoblotted with antibodies specific for the indicated proteins. D, HEK293T cells were transfected with GFP-tagged wild type Tiam1 or an empty vector. Cells were collected and lysed. Tiam1 was immunoprecipitated from whole cell extracts, and immunocomplexes were analyzed by immunoblotting with antibodies specific for the indicated proteins. E, arginine 447 in the WD40 repeat of ␤TrCP2 is required for the interaction with Tiam1. HEK293T cells were transfected as indicated and analyzed as in C. F, Tiam1, Skp1, Cul1, and Rbx1 were expressed in HEK293T in the absence or presence of ␤TrCP1 or an inactive ␤TrCP1-⌬F-box mutant. After immunopurification with anti-FLAG resin, an in vitro ubiquitylation assay of Tiam1 was performed. Samples were analyzed by immunoblotting with an anti-Tiam1 antibody. The bracket indicates a ladder of bands corresponding to polyubiquitylated Tiam1.
These results suggest that Tiam1 is a substrate of SCF ␤TrCP . To test whether SCF ␤TrCP targets Tiam1 for ubiquitin conjugation, we reconstituted the ubiquitylation of Tiam1 in vitro.

Tiam1 Degradation Regulates mTOR-S6K Signaling
F and G). Taken together, these results demonstrate that the association of Tiam1 with ␤TrCP requires the conserved degron motif SEFADSGIEGAT. As a second approach to examine whether phosphorylation of Tiam1 is required for the interaction with ␤TrCP, we employed an in vitro binding assay using immobilized synthetic phosphopeptides containing the ␤TrCP recognition domain of Tiam1. Peptides containing phosphorylated residues at positions Ser 329 and Ser 334 (Fig. 2H) or at positions Ser 334 and Thr 340 (Fig. 2I) efficiently associated with in vitro-translated ␤TrCP (but not with FBXW5), whereas the unphosphorylated peptides did not. These results indicate that phosphorylation of Ser 329 , Ser 334 , and Thr 340 directly mediates the interaction of Tiam1 with ␤TrCP.
To test whether the Tiam1 degron is phosphorylated in cells, FLAG-HA epitope-tagged Tiam1 immunoprecipitated from HEK293T cells was subjected to tryptic digestion followed by phosphopeptide enrichment by Ti4ϩ-IMAC and LC-MS/MS FIGURE 4. CK1 and the MAPK pathway control the ␤TrCP-mediated degradation of Tiam1. A, HEK293T cells were transfected with FLAG-tagged CK1␣, FLAG-tagged ␤TrCP1, or an empty vector. Forty-eight hours after transfection, cells were treated with MG132 for 5 h. Cells were then harvested and lysed. Whole cell extracts were immunoprecipitated (IP) with anti-FLAG resin and immunoblotted with antibodies specific for the indicated proteins. B and C, Tiam1 was immunopurified and dephosphorylated with lambda phosphatase prior to an in vitro kinase assay in the presence of purified CK1␣. A mock reaction (no kinase) was used as a negative control. Individual mixes were subsequently trypsinized and analyzed by mass spectrometry. The Tiam1 tryptic peptide TTQDVNAGEGSEFADSGIEGATTDTDLLSR was not found to be phosphorylated in the negative control (B). When CK1␣ was used in the in vitro kinase assay, the same peptide was found to be phosphorylated on Ser 329 (C). As shown, both peptide sequences can be clearly explained by their respective HCD MSMS spectrum (Mascot score 139 and 92), including the Ser(P) 329 site (PhosphoRS site probability ϭ 100.0%). In these figures, pS denotes phosphorylated serine, b denotes b ions, and y denotes y ions. D, HEK293T cells were transfected with FLAG-tagged ␤TrCP1. Forty-eight hours after transfection, cells were treated with MG132 for 5 h (when indicated) in the presence or absence of the indicated kinase inhibitors. Cells were then harvested and lysed. Whole cell extracts were immunoprecipitated with anti-FLAG resin and immunoblotted with antibodies specific for the indicated proteins. E, HEK293T cells were transfected with HA-tagged wild type Tiam1 or HA-tagged Tiam1(S329A/S334A). Forty-eight hours after transfection, cells were treated as in D. Whole cell extracts were processed as in D except that an anti-HA resin was used for immunoprecipitation. F, cells were treated with PMA for 4 h with or without the CK1 inhibitor D4476. Whole cell extracts were analyzed by immunoblotting. G, HEK293 cells were transfected with plasmids expressing HA-tagged wild type Tiam1 along with plasmids expressing the indicated kinases. Twenty-four hours after transfection, cells were collected and lysed. Whole cells extracts were analyzed by immunoblotting with antibodies specific for the indicated proteins. H, HEK293T cells were transfected with either HA-tagged wild type Tiam1 or HA-tagged Tiam1(S329A/S334A) along with Myc-tagged ubiquitin with or without CK1␣. Cells were harvested and lysed in 0.1% Triton X-100 lysis buffer. Whole cell extracts were denatured by adding 1% SDS and boiling for 10 min. SDS was quenched and diluted. Whole cell extracts were then immunoprecipitated with anti-HA resin and immunoblotted with anti-Myc antibodies. The bracket indicates a ladder of bands corresponding to polyubiquitylated Tiam1. I, HEK293 cells were treated with PMA in the absence or presence of the indicated compounds. Cells were collected at the indicated times and lysed. Whole cell extracts were analyzed by immunoblotting. J, HEK293T cells were transfected with FLAG-tagged ␤TrCP1 or FLAG-tagged ␤TrCP1(R474A). Forty-eight hours after transfection, cells were treated with MG132 for 5 h in the presence or absence of the MEK inhibitor U1026. Cells were then harvested and lysed. Whole cell extracts were immunoprecipitated with anti-FLAG resin and immunoblotted with antibodies specific for the indicated proteins. EV, empty vector. OCTOBER 3, 2014 • VOLUME 289 • NUMBER 40 JOURNAL OF BIOLOGICAL CHEMISTRY 27405 analysis. We recovered phosphopeptides containing Ser(P) 329 (Fig. 2J), Ser(P) 334 (Fig. 2K), and Thr(P) 341 (Fig. 2L), indicating that the Tiam1 degron is phosphorylated in cultured cells.

Tiam1 Degradation Regulates mTOR-S6K Signaling
Mitogens Induce the Degradation of Tiam1-Tiam1-Rac signaling controls a wide range of signaling pathways regulated by extracellular signals. While testing the effect of diverse stimuli on the abundance of Tiam1, we observed a decrease of Tiam1 levels in HEK293 cells treated with the potent mitogen phorbol 12-myristate 13-acetate (PMA; Fig. 3A). Mitogen-induced down-regulation of Tiam1 is transient because Tiam1 abundance goes back approximately to the initial levels 10 -16 h after PMA treatment. The reduction in Tiam1 levels was prevented when cells were treated with the proteasome inhibitor MG132, indicating that Tiam1 degradation in response to PMA is mediated by the proteasome (Fig. 3B). Similarly, Tiam1 protein levels decreased in a proteasome-dependent manner in HEK293 cells that were first deprived of serum for 48 h and then stimulated by the readdition of serum (Fig. 3C). The degradation of Tiam1 in response to mitogenic stimulation was observed also in other cell types, namely T98G cells (Fig. 3D) and MDCK cells (Fig. 3E).
Next, we examined whether the observed mitogen-induced degradation of Tiam1 is mediated by ␤TrCP. We silenced by RNAi the expression of both ␤TrCP1 and ␤TrCP2 (20 -24) in HEK293 cells, which were then treated with PMA. As shown in Fig. 3F, ␤TrCP knockdown inhibited the PMA-induced degradation of Tiam1. Ectopic expression of ␤TrCP with a deleted F-box motif (␤TrCP-⌬F), which has been shown to function as a dominant negative mutant (25)(26)(27)(28)(29), also prevented the degradation of Tiam1 (Fig. 3G). Moreover, the binding of ␤TrCP to endogenous Tiam1 was enhanced by PMA treatment (Fig. 3H). Altogether, these results indicate that mitogenic stimulation of cells triggers the ␤TrCP-mediated proteasomal degradation of Tiam1.
Casein Kinase 1 and MAPK Signaling Control the ␤TrCPmediated Degradation of Tiam1-In the Tiam1 immunopurification described above, we also retrieved three peptides (DIK-PDNFLMGIGR, MSTPVEVLCK, and AAQQAASSSGQGQ-QAQTPTGK) corresponding to casein kinase 1␣ (CK1␣) and one peptide (HPQLHIESK) corresponding to casein kinase 1⑀ (CK1⑀). First, we confirmed the interaction between Tiam1 and CK1␣ (Fig. 4A). Second, to test whether CK1␣ is able to phosphorylate the Tiam1 degron and pinpoint the specific Tiam1 site targeted by CK1␣, immunopurified, dephosphorylated Tiam1 was subjected to an in vitro kinase assay in the presence or absence of purified CK1␣ prior to mass spectrom-

Tiam1 Degradation Regulates mTOR-S6K Signaling
etry analysis. We identified phosphopeptides containing Ser(P) 329 in CK1␣-treated Tiam1 samples (Fig. 4, B and C). These phosphopeptides were not found in Tiam1 treated with other kinases or when no kinase was added to the reaction. Next, we assessed the possible involvement of CK1 in the ␤TrCP-dependent degradation of Tiam1. We employed the CK1 pharmacological inhibitors D4476 and IC261 to inactivate CK1 in HEK293T cells. As shown in Fig. 4 (D and E), the Tiam1-␤TrCP binding was abolished by both D4476 and IC261, suggesting that CK1 is required for the ␤TrCP-dependent degradation of Tiam1. Indeed, pharmacological inhibition of CK1 prevented the degradation of Tiam1 in response to PMA treatment (Fig. 4F). Accordingly, in cultured cells, Tiam1 degradation (Fig. 4G) and ubiquitylation (Fig. 4H) were stimulated by the ectopic expression of CK1␣.
The finding that mitogens induce the CK1-and ␤TrCP-mediated degradation of Tiam1 prompted us to test whether MAPKs control Tiam1 proteolysis. Fig. 4I shows that pharmacological inhibition of MEK1 and MEK2, two protein kinases of the MAPK cascade known to be activated by mitogenic stimuli, blocked the PMA-induced degradation of Tiam1 to the same extent of MG132. Accordingly, inhibition of MEK1 and MEK2 reduced the interaction between ␤TrCP and Tiam1 (Fig. 4J).
Tiam1 Degradation Is Required for the Termination of mTOR-S6K Signaling-To investigate the biological significance of Tiam1 degradation, physiological levels of wild type Tiam1 and the Tiam1(S239A/S334A) mutant were expressed in HEK293 cells. Tiam1(S239A/S334A) and the Tiam1 mutant truncated at the N terminus (C1199) lacking the ␤TrCP binding domain were resistant to the degradation induced by mitogenic stimulation, as indicated by the half-life experiment shown in Fig. 5A.
Because it has been shown that both Tiam1 and Rac1 control the mTOR-S6K signaling pathway, which mediates the mitogenic response in cells (30 -32), we analyzed the activation of mTOR-S6K signaling in response to mitogenic stimulation in cell expressing wild type Tiam1 and the nondegradable Tiam1(S239A/S334A) mutant. As shown in Fig. 5B, mitogenic stimulation of cells expressing wild type Tiam1 resulted in an increase of the mTOR-mediated phosphorylation of p70-S6K (Thr 389 ) and its isoform p85-S6K (Thr 412 ), which then rapidly decreased. In contrast, cells expressing the nondegradable Tiam1(S239A/S334A) mutant displayed a sustained (at least up to 5 h after PMA treatment) phosphorylation of p70-S6K (Thr 389 ) and p85-S6K (Thr 412 ) in response to mitogenic stimulation. No remarkable effect on the phosphorylation of p70-S6K (Thr 389 ) and p85-S6K (Thr 412 ) was observed in asynchronously growing cells (Fig. 5C). The expression of the degradation-resistant Tiam1(S239A/S334A) mutant had a similar effect on the mitogen-induced activating phosphorylation of additional residues of p70-S6K (Thr 421 /Ser 424 ) and p85-S6K (Thr 444 /Ser 447 ) (Fig. 5B). Similar results were  OCTOBER 3, 2014 • VOLUME 289 • NUMBER 40 obtained when serum was used to stimulate cells expressing wild type Tiam1 or the Tiam1(S239A/S334A) mutant (Fig.  5D). In agreement with previous reports (30), pharmacological inhibition of Rac activity prevented the induction of S6K phosphorylation following mitogenic stimulation, suggesting that the mitogen-induced activation of the mTOR-S6K signaling pathway is dependent on Rac activity (Fig. 5E). Taken together, these results demonstrate that failure to degrade Tiam1 in response to mitogens results in prolonged activation of the mTOR/S6K signaling.

Tiam1 Degradation Regulates mTOR-S6K Signaling
Failure to Degrade Tiam1 Results in Loss of Cell Viability and Increased Apoptosis-Finally, we investigated the effect of defective degradation of Tiam1 on cell growth and survival. After mitogenic stimulation, cells expressing Tiam1(S239A/ S334A) or Tiam1-C1199 displayed reduced cell viability when compared with cells expressing wild type Tiam1 (Fig. 6, A and  B). Moreover, failure to degrade Tiam1 resulted in apoptotic cell death as shown by the induction of the cleaved active form of Caspase 3 (Fig. 6, C and D).

DISCUSSION
Here we have shown that Tiam1 is a novel substrate of the SCF ␤TrCP ubiquitin ligase, identified a conserved phosphodegron at the N terminus of Tiam1 that is required for Tiam1 binding to ␤TrCP, and demonstrated that SCF ␤TrCP targets Tiam1 for proteasome-dependent degradation in response to mitogenic stimulation. We have also found that the mitogeninduced degradation of Tiam1 is mediated by CK1␣, which phosphorylates a residue within the Tiam1 phosphodegron. Tiam1 destruction is required for terminating the activation of the mTOR-S6K signaling pathway following mitogenic stimulation. Indeed, expression of a Tiam1 mutant unable to bind ␤TrCP results in sustained phosphorylation of S6K, a substrate of mTOR. Failure to degrade Tiam1 leads to loss of cell viability caused by increased apoptosis. Interestingly, it has been recently reported that constitutive mTOR-S6K signaling sensitizes cells to p53-dependent cell death in response to stress conditions (33). In agreement with these studies, a recent report has shown that cells expressing the degradation-resistant Tiam1-C1199 mutant are more sensitive to DNA-damaging drug-induced apoptosis (34).
We have shown that the ␤TrCP-mediated degradation of Tiam1 is blocked by pharmacological inhibition of MEK. Accordingly, the Malliri group (35) has demonstrated that ERK1 and ERK2 associate with Tiam1 and that ERK activation is required for the v-Src-induced degradation of Tiam1. The involvement of the MEK-ERK pathway in the destruction of Tiam1 via ␤TrCP also suggests that the MEK-ERK-dependent phosphorylation of Tiam1 could prime the phosphorylation of the Tiam1 degron by CK1, as has been shown for other ␤TrCP substrates (16) (36,37). Phospho-specific antibodies against the Tiam1 degron motif ( 329 pSEFADpSGIEGApT 340 ) are required to test(bothinvitroandinculturedcells)whetherTiam1isphosphorylated by CK1 on its degron following initial phosphorylation by MEK-ERK on different sites. In conclusion, the finding that the degradation of Tiam1, induced by CK1 in cooperation with the MAPK cascade, is needed to terminate mTOR-S6K signaling sug-gests a new mechanism by which the MAPK cascade controls the timing of activation of the mTOR-S6K signaling pathway.