KIF14 Negatively Regulates Rap1a–Radil Signaling During Breast Cancer Progression

JCB: Article KIF14 negatively regulates Rap1a–Radil signaling during breast cancer progression Syed M. Ahmed,1 Brigitte L. Thériault,4 Maruti Uppalapati,2 Catherine W.N. Chiu,1 Brenda L. Gallie,4 Sachdev S. Sidhu,2 and Stéphane Angers1,3 1Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, 2Terrence Donnelly Center for Cellular and Biomolecular Research, and 3Department of Biochemistry, Faculty of Medicine, University of Toronto, Toronto, Ontario M5S 1A1, Canada 4Campbell Family Cancer Research Institute, Ontario Cancer Institute, University Health Network, Toronto, Ontario M5G 2M9, Canada he small GTPase Rap1 regulates inside-out integrin tethering Radil on microtubules. The depletion of KIF14 activation and thereby influences cell adhesion, mi- led to increased cell spreading, altered focal adhesion dy- T gration, and polarity. Several Rap1 effectors have namics, and inhibition of cell migration and invasion. We been described to mediate the cellular effects of Rap1 in a also show that Radil is important for breast cancer cell context-dependent manner. Radil is emerging as an im- proliferation and for metastasis in mice. Our findings pro- portant Rap effector implicated in cell spreading and vide evidence that the concurrent up-regulation of Rap1 migration, but the molecular mechanisms underlying its activity and increased KIF14 levels in several cancers is functions are unclear. We report here that the kinesin KIF14 needed to reach optimal levels of Rap1–Radil signaling, associates with the PDZ domain of Radil and negatively integrin activation, and cell–matrix adhesiveness required regulates Rap1-mediated inside-out integrin activation by for tumor progression. Introduction The small G-protein Rap1 is an important mediator of integrin Rap1a-mediated inside-out activation of integrins, adhesion, and inside-out signaling, which plays a pivotal role in adhesion, spreading of human fibrosarcoma cells (Ahmed et al., 2010). Radil spreading, and migration of cells (Bos et al., 2003; Arthur et al., is also known to have important functions in Epac1-mediated 2004; Kinashi and Katagiri, 2004, 2005; Bos, 2005). Rap1 acts spreading of lung carcinoma cells (Ross et al., 2011) and to as a molecular switch that cycles between active GTP-bound be indispensable for the migration of neural crest cells during and inactive GDP-bound states. Rap1 activity is regulated zebrafish development (Smolen et al., 2007). by guanine nucleotide exchange factors (GEFs) such as Epac1 The control of cell–matrix adhesion plays a fundamental (de Rooij et al., 1998) and GTPase activating proteins (GAPs) role in controlling cancer cell migration during metastasis THE JOURNAL OF CELL BIOLOGY such as Rap1GAP (Rubinfeld et al., 1991). Upon activation, (McLean et al., 2005; Desgrosellier and Cheresh, 2010; Arjonen Rap1 has the ability to increase the affinity of integrins for their et al., 2011). The implication of Rap1 signaling in the modula- extracellular matrix (ECM) ligands and to promote their clus- tion of integrin activity has thus provided a framework to study tering (Sebzda et al., 2002; Lafuente et al., 2004; Han et al., its implication in tumor progression. Both hyper-activation as 2006; Kim et al., 2011). In recent years the identification and well as decreased Rap1 activity is known to affect the migration characterization of downstream Rap effector proteins such as of breast, melanoma, and prostate cancer cells (Bailey et al., RIAM (Lafuente et al., 2004), RapL (Katagiri et al., 2003), 2009; Zheng et al., 2009; Kim et al., 2012). This highlights that Krit1 (Glading et al., 2007), AF-6 (Boettner et al., 2000), and precise control of cellular adhesion by Rap1 and its effectors is Radil (Smolen et al., 2007) have shed light on the molecular required for efficient cell movements. This requirement for the mechanisms underlying the cellular effects mediated by Rap1. fine-tuning of Rap1-mediated inside-out signaling for optimal We previously identified the Rap1 effector Radil as a protein control of cell–matrix adhesion implies the existence of pos- associating with G subunits of heterotrimeric G-proteins itive and negative mechanisms of regulation. Although how (Ahmed et al., 2010). Radil was found to be required for the © 2012 Ahmed et al. This article is distributed under the terms of an Attribution– Noncommercial–Share Alike–No Mirror Sites license for the first six months after the pub- Correspondence to Stéphane Angers: [email protected] lication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, Abbreviation used in this paper: GAP, GTPase-activating protein. as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). The Rockefeller University Press $30.00 J. Cell Biol. Vol. 199 No. 6 951–967 www.jcb.org/cgi/doi/10.1083/jcb.201206051 JCB 951 Rap1 leads to integrin inside-out activation is becoming better preferred C-terminal peptides recognized by the Radil PDZ defined, the identification of mechanisms buffering or nega- domain. We panned a phage-displayed peptide library with a tively impinging this process is not well understood. Such regu- recombinant Radil PDZ domain fused to GST (Fig. 1 A) and lators may be especially relevant in the context of aggressive repeated multiple rounds of binding selection. Binding phages cancer cells to optimally adjust Rap1 activity where it is known were isolated and the sequences of the displayed peptides were to be elevated (Lorenowicz et al., 2008; Lyle et al., 2008; determined (Fig. 1 A). The analysis of the 25 best binding Bailey et al., 2009; Zheng et al., 2009; Freeman et al., 2010; sequences revealed that the Radil PDZ domain recognizes Huang et al., 2012). hydrophobic C-terminal ligands with a strong consensus to the Kinesins are molecular motors associated with intracel- sequence [FI]-[FWT]-WV for the last four amino acids as rep- lular transport (Hirokawa et al., 2009; Verhey and Hammond, resented by the motif enrichment diagram in Fig. 1 A. Most 2009). Kinesin superfamily proteins (KIFs) are important mo- PDZ domains prefer ligands containing either S/T (class I) or lecular motors that transport various cargoes along micro- hydrophobic amino acids (class II) at the 2 position (third tubules tracks. Several kinesins have been implicated in cancer residue from the end; Tonikian et al., 2008). Radil appears to progression due to their role in mitotic cell division (Huszar et al., contain an atypical PDZ domain because it can bind to both 2009). Recently, kinesins were uncovered as playing important ligands classes. Because the Radil PDZ domain can accom- regulatory roles in adhesion and migration of cells (Uchiyama modate both hydrophobic and hydrophilic residues at the et al., 2010; Zhang et al., 2010). Blocking kinesin-1 activity 2 position, we performed a BLAST search against the Swiss- using inactivating antibodies was also shown to lead to increase Prot human proteome database to assemble a list of natural pro- in the size and number of substrate adhesions (Kaverina et al., teins with C termini matching the consensus sequence [FI]-x-WV. 1997; Krylyshkina et al., 2002). Although the precise mecha- We compared this list of putative Radil PDZ domain ligands to nisms are unclear, kinesins were suggested to control the de- a list of proteins that we identified in FLAG-Radil complexes livery of factors at adhesion sites to retard their growth or using immunoprecipitation and mass spectrometry (Fig. 1 A; promote their disassembly. KIF14 was initially characterized Table S1), and we found that KIF14 was present in both lists. as a protein involved in cytokinesis by interacting with protein- Consistent with a physical association between these pro- regulating cytokinesis-1 (PRC1) and Citron kinase (Gruneberg teins, the immunoprecipitation of Radil from HEK293T cells et al., 2006). KIF14 was also demonstrated to be highly up- led to the coprecipitation of KIF14 (Fig. 1 B). The phage regulated in several cancers including retinoblastomas, breast display results suggest that KIF14 binds to the PDZ domain cancers, lung cancers, and ovarian cancers and its high expres- of Radil. To confirm this result in a cellular context, lysates sion levels has been clinically correlated with increased breast from control HEK293T or from cells stably expressing cancer invasiveness and mortality (Corson et al., 2005, 2007; Strep-HA-Radil or Strep-HA-RadilPDZ were subjected to Corson and Gallie, 2006; Thériault et al., 2012). affinity purification using Sepharose-streptavidin followed We previously established that the C-terminal PDZ by Western blotting using antibodies specific to KIF14. domain of Radil was critical for its function, but the identity Whereas endogenous KIF14 copurifies with full-length Radil, of the protein(s) binding to the Radil PDZ domain and how it is absent in control or RadilPDZ affinity-purified samples it contributed to Rap1–Radil signaling was, however, not (Fig. 1 C, compare lane 2 with lanes 1 and 3). To validate that addressed. PDZ domains are present in many scaffolding KIF14 interacts with Radil via its atypical PDZ binding motif, proteins and are involved in the organization of multi-protein we coexpressed Strep-HA-Radil with wild-type KIF14 or a complexes important for numerous biological processes includ- mutant KIF14-IQAA in which the C-terminal tryptophan and ing cell adhesion, spreading, migration, and polarization (Hall valine were

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