A number of key regulatory proteins contain one or two copies of the WW domain known to mediate protein–protein interaction via proline-rich motifs, such as PPxY. The Hippo pathway components take advantage of this module to transduce tumor suppressor signaling. It is becoming evident that tyrosine phosphorylation is a critical regulator of the WW proteins. Here, we review the current knowledge on the involved tyrosine kinases and their roles in regulating the WW proteins.
SudolM. Yes-associated protein (YAP65) is a proline-rich phosphoprotein that binds to the SH3 domain of the Yes proto-oncogene product. Oncogene1994; 9: 2145–52.
2.
BorkPSudolM. The WW domain: a signalling site in dystrophin. Trends Biochem Sci1994; 19: 531–3.
3.
SudolMBorkPEinbondAKasturyKDruckTNegriniMHuebnerKLehmanD. Characterization of the mammalian YAP (Yes-associated protein) gene and its role in defining a novel protein module, the WW domain. J Biol Chem1995; 270: 14733–41.
4.
MaciasMJWiesnerSSudolM. WW and SH3 domains, two different scaffolds to recognize proline-rich ligands. FEBS Lett2002; 513: 30–7.
5.
HuHColumbusJZhangYWuDLianLYangSGoodwinJLuczakCCarterMChenLJamesMDavisRSudolMRodwellJHerreroJJ. A map of WW domain family interactions. Proteomics2004; 4: 643–55.
6.
OtteLWiedemannUSchlegelBPiresJRBeyermannMSchmiederPKrauseGVolkmer-EngertRSchneider-MergenerJOschkinatH. WW domain sequence activity relationships identified using ligand recognition propensities of 42 WW domains. Protein Sci: Publication Protein Soc2003; 12: 491–500.
7.
Del MareSSalahZAqeilanRI. WWOX: its genomics, partners, and functions. J Cell Biochem2009; 108: 737–45.
8.
AqeilanRIPekarskyYHerreroJJPalamarchukALetofskyJDruckTTrapassoFHanSYMelinoGHuebnerKCroceCM. Functional association between Wwox tumor suppressor protein and p73, a p53 homolog. Proceedings Natl Acad Sci USA2004; 101: 4401–6.
9.
StranoSMunarrizERossiMCastagnoliLShaulYSacchiAOrenMSudolMCesareniGBlandinoG. Physical interaction with Yes-associated protein enhances p73 transcriptional activity. J Biol Chem2001; 276: 15164–73.
AqeilanRIPalamarchukAWeigelRJHerreroJJPekarskyYCroceCM. Physical and functional interactions between the Wwox tumor suppressor protein and the AP-2gamma transcription factor. Cancer Res2004; 64: 8256–61.
12.
HsuLJSchultzLHongQVan MoerKHeathJLiMYLaiFJLinSRLeeMHLoCPLinYSChenSTChangNS. Transforming growth factor beta1 signaling via interaction with cell surface Hyal-2 and recruitment of WWOX/WOX1. J Biol Chem2009; 284: 16049–59.
13.
ChangNSDohertyJEnsignALewisJHeathJSchultzLChenSTOppermannU. Molecular mechanisms underlying WOX1 activation during apoptotic and stress responses. Biochem Pharmacol2003; 66: 1347–54.
14.
ChangNSDohertyJEnsignASchultzLHsuLJHongQ. WOX1 is essential for tumor necrosis factor-, UV light-, staurosporine-, and p53-mediated cell death, and its tyrosine 33-phosphorylated form binds and stabilizes serine 46-phosphorylated p53. J Biol Chem2005; 280: 43100–8.
15.
ChangNSDohertyJEnsignA. JNK1 physically interacts with WW domain-containing oxidoreductase (WOX1) and inhibits WOX1-mediated apoptosis. J Biol Chem2003; 278: 9195–202.
16.
IlsleyJLSudolMWinderSJ. The interaction of dystrophin with beta-dystroglycan is regulated by tyrosine phosphorylation. Cell Signal2001; 13: 625–32.
17.
FujikawaAFukadaMMakiokaYSuzukiRChowJPMatsumotoMNodaM. Consensus substrate sequence for protein-tyrosine phosphatase receptor type Z. J Biol Chem2011; 286: 37137–46.
18.
HornbeckPVKornhauserJMTkachevSZhangBSkrzypekEMurrayBLathamVSullivanM. PhosphoSitePlus: a comprehensive resource for investigating the structure and function of experimentally determined post-translational modifications in man and mouse. Nucleic Acids Res2012; 40: D261–70.
19.
LiuXYangNFigelSAWilsonKEMorrisonCDGelmanIHZhangJ. PTPN14 interacts with and negatively regulates the oncogenic function of YAP. Oncogene2013; 32: 1266–73.
20.
HuangJMNagatomoISuzukiEMizunoTKumagaiTBerezovAZhangHKarlanBGreeneMIWangQ. YAP modifies cancer cell sensitivity to EGFR and survivin inhibitors and is negatively regulated by the non-receptor type protein tyrosine phosphatase 14. Oncogene2013; 32: 2220–9.
21.
MichaloglouCLehmannWMartinTDelaunayCHueberABarysLNiuHBillyEWartmannMItoMWilsonCJDiganMEBauerAVosholHChristoforiGSellersWRHofmannFSchmelzleT. The tyrosine phosphatase PTPN14 is a negative regulator of YAP activity. PloS ONE2013; 8: e61916–e61916.
22.
WilsonKELiYWYangNShenHOrillionARZhangJ. PTPN14 Forms a Complex with Kibra and LATS1 proteins and negatively regulates the YAP oncogenic function. J Biol Chem2014; 289: 23693–700.
23.
TsutsumiRMasoudiMTakahashiAFujiiYHayashiTKikuchiISatouYTairaMHatakeyamaM. YAP and TAZ, Hippo signaling targets, act as a rheostat for nuclear SHP2 function. Developmen Cell2013; 26: 658–65.
24.
ShanzerMRicardo-LaxIKeshetRReuvenNShaulY. The Polyomavirus Middle T-antigen oncogene activates the Hippo-pathway tumor suppressor Lats in a Src-dependent manner. Oncogene2014. Nov 3. doi: 10.1038/onc.2014.347. [Epub ahead of print].
25.
XingWKimJWergedalJChenSTMohanS. Ephrin B1 regulates bone marrow stromal cell differentiation and bone formation by influencing TAZ transactivation via complex formation with NHERF1. Molecular Cellular Biol2010; 30: 711–21.
26.
PoernbacherIBaumgartnerRMaradaSKEdwardsKStockerH. Drosophila Pez acts in Hippo signaling to restrict intestinal stem cell proliferation. Curr Biol2012; 22: 389–96.
27.
ZaidiSKSullivanAJMedinaRItoYvan WijnenAJSteinJLLianJBSteinGS. Tyrosine phosphorylation controls Runx2-mediated subnuclear targeting of YAP to repress transcription. EMBO J2004; 23: 790–9.
28.
KomuroANagaiMNavinNESudolM. WW domain-containing protein YAP associates with ErbB-4 and acts as a co-transcriptional activator for the carboxyl-terminal fragment of ErbB-4 that translocates to the nucleus. J Biol Chem2003; 278: 33334–41.
29.
OmerovicJPuggioniEMNapoletanoSViscoVFraioliRFratiLGulinoAAlimandiM. Ligand-regulated association of ErbB-4 to the transcriptional co-activator YAP65 controls transcription at the nuclear level. Experiment Cell Res2004; 294: 469–79.
30.
AqeilanRIDonatiVPalamarchukATrapassoFKaouMPekarskyYSudolMCroceCM. WW domain-containing proteins, WWOX and YAP, compete for interaction with ErbB-4 and modulate its transcriptional function. Cancer Res2005; 65: 6764–72.
31.
LevyDAdamovichYReuvenNShaulY. Yap1 phosphorylation by c-Abl is a critical step in selective activation of proapoptotic genes in response to DNA damage. Mol Cell2008; 29: 350–61.
32.
RosenbluhJNijhawanDCoxAGLiXNealJTSchaferEJZackTIWangXTsherniakASchinzelACShaoDDSchumacherSEWeirBAVazquezFCowleyGSRootDEMesirovJPBeroukhimRKuoCJGoesslingWHahnWC. beta-Catenin-driven cancers require a YAP1 transcriptional complex for survival and tumorigenesis. Cell2012; 151: 1457–73.
33.
TammCBowerNAnnerenC. Regulation of mouse embryonic stem cell self-renewal by a Yes-YAP-TEAD2 signaling pathway downstream of LIF. J Cell Sci2011; 124: 1136–44.
RussoTFaraonioRMinopoliGDe CandiaPDe RenzisSZambranoN. Fe65 and the protein network centered around the cytosolic domain of the Alzheimer's beta-amyloid precursor protein. FEBS Lett1998; 434: 1–7.
36.
PerkintonMSStandenCLLauKFKesavapanySByersHLWardMMcLoughlinDMMillerCC. The c-Abl tyrosine kinase phosphorylates the Fe65 adaptor protein to stimulate Fe65/amyloid precursor protein nuclear signaling. J Biol Chem2004; 279: 22084–91.
37.
HarveyKFKumarS. Nedd4-like proteins: an emerging family of ubiquitin-protein ligases implicated in diverse cellular functions. Trends Cell Biol1999; 9: 166–9.
38.
AnHKristDTStatsyukAV. Crosstalk between kinases and Nedd4 family ubiquitin ligases. Mol Biosyst2014; 10: 1643–57.
39.
AnHKristDTStatsyukAV. Crosstalk between kinases and Nedd4 family ubiquitin ligases. Mol Biosyst2014; 10: 1643–57.
40.
SkouloudakiKWalzG. YAP1 recruits c-Abl to protect angiomotin-like 1 from Nedd4-mediated degradation. PloS ONE2012; 7: e35735–e35735.
41.
Moleirinho S, Guerrant W, Kissil JL. The Angiomotins – From discovery to function. FEBS letters. 2014.
42.
PersaudAAlbertsPMariSTongJMurchieRMasperoESafiFMoranMPoloSRotinD. Tyrosine phosphorylation of NEDD4 activates its ubiquitin ligase activity. Sci Signal2014; 7: ra95–ra95.
43.
YimEKPengGDaiHHuRLiKLuYMillsGBMeric-BernstamFHennessyBTCravenRJLinSY. Rak functions as a tumor suppressor by regulating PTEN protein stability and function. Cancer Cell2009; 15: 304–14.
44.
GaoMLabudaTXiaYGallagherEFangDLiuYCKarinM. Jun turnover is controlled through JNK-dependent phosphorylation of the E3 ligase Itch. Science2004; 306: 271–5.
45.
RossiMAqeilanRINealeMCandiESalomoniPKnightRACroceCMMelinoG. The E3 ubiquitin ligase Itch controls the protein stability of p63. Proc Natl Acad Sci USA2006; 103: 12753–8.
46.
SalahZMelinoGAqeilanRI. Negative regulation of the Hippo pathway by E3 ubiquitin ligase ITCH is sufficient to promote tumorigenicity. Cancer Res2011; 71: 2010–20.
47.
ZhangPWangCGaoKWangDMaoJAnJXuCWuDYuHLiuJOYuL. The ubiquitin ligase itch regulates apoptosis by targeting thioredoxin-interacting protein for ubiquitin-dependent degradation. J Biol Chem2010; 285: 8869–79.
48.
GallagherEGaoMLiuYCKarinM. Activation of the E3 ubiquitin ligase Itch through a phosphorylation-induced conformational change. Proc Natl Acad Sci USA2006; 103: 1717–22.
49.
YangCZhouWJeonMSDemydenkoDHaradaYZhouHLiuYC. Negative regulation of the E3 ubiquitin ligase itch via Fyn-mediated tyrosine phosphorylation. Mol Cell2006; 21: 135–41.
50.
GaoBLeeSMFangD. The tyrosine kinase c-Abl protects c-Jun from ubiquitination-mediated degradation in T cells. J Biol Chem2006; 281: 29711–8.
51.
MahajanNPWhangYEMohlerJLEarpHS. Activated tyrosine kinase Ack1 promotes prostate tumorigenesis: role of Ack1 in polyubiquitination of tumor suppressor Wwox. Cancer Res2005; 65: 10514–23.
52.
ZhaoBLiLTumanengKWangCYGuanKL. A coordinated phosphorylation by Lats and CK1 regulates YAP stability through SCF(beta-TRCP). Genes Develop2010; 24: 72–85.
53.
LiuCYZhaZYZhouXZhangHHuangWZhaoDLiTChanSWLimCJHongWZhaoSXiongYLeiQYGuanKL. The hippo tumor pathway promotes TAZ degradation by phosphorylating a phosphodegron and recruiting the SCF{beta}-TrCP E3 ligase. J Biol Chem2010; 285: 37159–69.
54.
LevyDAdamovichYReuvenNShaulY. The Yes-associated protein 1 stabilizes p73 by preventing Itch-mediated ubiquitination of p73. Cell death Differentiation2007; 14: 743–51.
55.
DanoviSARossiMGudmundsdottirKYuanMMelinoGBasuS. Yes-associated protein (YAP) is a critical mediator of c-Jun-dependent apoptosis. Cell Death Differentiation2008; 15: 217–9.
56.
LevyDReuvenNShaulY. A regulatory circuit controlling Itch-mediated p73 degradation by Runx. J Biol Chem2008; 283: 27462–8.
57.
WhiteCDErdemirHHSacksDB. IQGAP1 and its binding proteins control diverse biological functions. Cell Signal2012; 24: 826–34.
58.
RoyMLiZSacksDB. IQGAP1 binds ERK2 and modulates its activity. J Biol Chem2004; 279: 17329–37.
HeilANazmiARKoltzscherMPoeterMAustermannJAssardNBaudierJKaibuchiKGerkeV. S100P is a novel interaction partner and regulator of IQGAP1. J Biol Chem2011; 286: 7227–38.
63.
Mo JS, Park HW, Guan KL. The Hippo signaling pathway in stem cell biology and cancer. EMBO reports 2014;15:642–56.
64.
ZhaoBLiLLeiQGuanKL. The Hippo-YAP pathway in organ size control and tumorigenesis: an updated version. Genes Develop2010; 24: 862–74.
65.
SalahZAqeilanRI. WW domain interactions regulate the Hippo tumor suppressor pathway. Cell Death Dis2011; 2: e172–e172.
66.
SudolMHarveyKF. Modularity in the Hippo signaling pathway. Trends Biochem Sci2010; 35: 627–33.
67.
JinJXieXChenCParkJGStarkCJamesDAOlhovskyMLindingRMaoYPawsonT. Eukaryotic protein domains as functional units of cellular evolution. Sci Signal2009; 2: ra76–ra76.
68.
KeshetRAdlerJRicardo-LaxIShanzerMPoratZReuvenNShaulY. c-Abl antagonizes the Yap oncogenic function. Cell Death Differ2014. Oct 31. doi: 10.1038/cdd.2014.182. [Epub ahead of print].
69.
HuangXPoyFZhangRJoachimiakASudolMEckMJ. Structure of a WW domain containing fragment of dystrophin in complex with beta-dystroglycan. Nat Struct Biol2000; 7: 634–8.
70.
MatsuiYLaiZC. Mutual regulation between Hippo signaling and actin cytoskeleton. Protein Cell2013; 4: 904–10.
71.
LowBCPanCQShivashankarGVBershadskyASudolMSheetzM. YAP/TAZ as mechanosensors and mechanotransducers in regulating organ size and tumor growth. FEBS Lett2014; 588: 2663–70.
72.
GasparPTaponN. Sensing the local environment: actin architecture and Hippo signalling. Curr Opin Cell Biol2014; 31C: 74–83.