The spectraplakin Dystonin antagonizes YAP activity and suppresses tumourigenesis

Aberrant expression of the Spectraplakin Dystonin (DST) has been observed in various cancers, including those of the breast. However, little is known about its role in carcinogenesis. In this report, we demonstrate that Dystonin is a candidate tumour suppressor in breast cancer and provide an underlying molecular mechanism. We show that in MCF10A cells, Dystonin is necessary to restrain cell growth, anchorage-independent growth, self-renewal properties and resistance to doxorubicin. Strikingly, while Dystonin maintains focal adhesion integrity, promotes cell spreading and cell-substratum adhesion, it prevents Zyxin accumulation, stabilizes LATS and restricts YAP activation. Moreover, treating DST-depleted MCF10A cells with the YAP inhibitor Verteporfin prevents their growth. In vivo, the Drosophila Dystonin Short stop also restricts tissue growth by limiting Yorkie activity. As the two Dystonin isoforms BPAG1eA and BPAG1e are necessary to inhibit the acquisition of transformed features and are both downregulated in breast tumour samples and in MCF10A cells with conditional induction of the Src proto-oncogene, they could function as the predominant Dystonin tumour suppressor variants in breast epithelial cells. Thus, their loss could deem as promising prognostic biomarkers for breast cancer.

DST is necessary to prevent transformation in MCF10A cells. To determine if DST acts as a bona-fide tumour suppressor, we generated stable MCF10A cells carrying Tet-inducible shRNA against all DST isoforms (shDST). Treating these cells with Tet reduced DST mRNA levels by 90% compared to control Tet-treated MCF10A-shLuc (shLuc) cells ( Fig. 2A). Knocking down DST was sufficient to increase the colony-forming ability of MCF10A cells in clonogenic assays (Fig. 2B) and significantly upregulated Cyclin D1 mRNA levels (Fig. 2C), a known regulator of G1 to S phase progression 41 . Moreover, Tet-treated shDST cells produced significantly higher number of anchorage-independent colonies in soft agar compared to those expressing shLuc cells (Fig. 2D). Furthermore, knocking down DST also increased the mammosphere-forming abilities of MCF10A cells, as well as mammospheres size that were on average 1.4 times bigger (Fig. 2E). Finally, depleting DST conferred cells with significantly increased survival potential upon exposure to 250 nM of Doxorubicin (Fig. 2F), suggesting that the downregulation of DST promotes chemoresistance to these cells. To discard the possibility that the transformed phenotype of Tet-treated shDST cells resulted from off-target effects, we generated stable MCF10A cells expressing independent Tet-inducible shRNA against all DST isoforms (shDST#2). Treatment of these cells with Tet reduced DST mRNA levels by 55% ( Supplementary Fig. S1), similar to Src's effect on DST levels in MCF10A-ER-Src cells (Fig. 1B). This was sufficient to promote the acquisition of transformation features, as Tet-treated shDST#2 cells showed increased abilities to grow as colonies in clonogenic assays and to form mammospheres compared to those expressing shLuc ( Supplementary Fig. S1). All together, we conclude that the presence of DST is necessary in MCF10A cells to restrict the gain of transformed features.
DSt restricts YAp activity. Zyxin is known to induce YAP/Yki activity by destabilizing LATS/Wts and by linking F-actin regulation to Yki-mediated tissue growth [26][27][28] . We therefore tested whether DST prevents cellular transformation through the regulation of Hippo pathway activity. Accordingly, LATS levels were significantly lower in Tet-treated shDST cells compared to those expressing shLuc ( Fig. 4A and Supplementary Fig. S2). Moreover, qRT-PCR revealed that cells knocked down for DST expressed higher levels of the YAP/TAZ target genes Connective Tissue Growth Factor (CTGF), Cysteine rich angiogenic inducer 61 (CYR61) and Integrin β6 (ITGB6) (Fig. 4B). To confirm the effect of DST on YAP/TAZ transcriptional activity, we analysed the activity of a MCAT (muscle C, A and T)-dependent luciferase reporter (MCAT-Luc), which contains TEAD binding sites and responds to YAP/TAZ activity 44 . Tet-treated shDST cells showed higher levels of Luciferase activity compared to those grown in the absence of Tet (Fig. 4C). Furthermore, knocking down DST significantly increased the percentage of cells with YAP localized predominantly in the nucleus (Fig. 4D). Thus, DST stabilizes LATS protein levels, limits YAP translocation into the nucleus and the upregulation of YAP target genes.
We then tested if YAP potentiates the growth of DST-depleted cells by treating cells with the YAP inhibitor Verteporfin (VP), which blocks the interaction between YAP and the transcription factor TEAD, therein repressing YAP's function 45 . Consistent with a role of YAP in promoting the transformation of DST-depleted cells, VP treatment downregulated CTGF, CYR61 and ITGB6 in both, shLuc-and shDST-expressing cells, compared to those treated with DMSO (Fig. 4E). Moreover, VP treatment reduced the growth rate of Tet-treated shLuc-and shDST cells (Fig. 4F). These observations suggest that DST prevents cellular transformation by limiting YAP activity.
In vivo, the Drosophila DSt Shot restricts tissue growth by limiting Yki activity. DST is evolutionarily well conserved between human and Drosophila 31 . Reminiscent to DST's effect on limiting the growth of MCF10A cells, expressing double strand RNA (dsRNA) directed against the Drosophila DST orthologue Shot (shot-RNAi) is sufficient to induce overgrowth in the distal wing imaginal disc epithelium. Conversely, overexpressing the full-length Shot-PE isoform fused to GFP (ShotL(A)::GFP), which can fully or partially rescue all shot mutant phenotypes tested so far 46 , reduces distal wing disc growth 33 . To determine if Shot prevents tissue overgrowth by limiting the activity of the YAP orthologue Yki in vivo, we analysed the effect of overexpressing wts or of knocking down yki on the overgrowth of distal wing discs carrying UAS-shot-RNAi expressed under nubbin-(nub)-Gal4 control. As the expression of UAS transgenes can vary based on the number of Gal4 transcriptional activator available per UAS transgenes, experiments were performed ensuring that all genetic backgrounds contained the same number of UAS transgenes, which were normalized using UAS-GFP, UAS-mCherry and UAS-RFP. As reported previously 33 , knocking down shot increased significantly the ratio between the nub > GFP-expressing area and the total wing disc area (Fig. 5B,G,H), as compared to control discs expressing GFP, mCherry and RFP (Fig. 5A,G,H). Overexpressing wts (wts + ) (Fig. 5D,G) or knocking down yki (yki-RNAi) (Fig. 5F,H) in nub > shot-RNAi-expressing discs drastically prevented the overgrowth of these tissues, which were even smaller that wing discs overexpressing wts (Fig. 5C,G) or yki-RNAi (Fig. 5E,H). Thus, the overgrowth of shot-depleted wing discs is dependent on Yki activity.
We then tested if expressing shot-RNAi or overexpressing ShotL(A)::GFP affects the expression of Yki target genes in the posterior wing disc compartment using the hedgehog-Gal4 (hh-Gal4) driver, thus allowing comparison to the wild type anterior compartment. In control GFP-expressing wing discs, the Yki target gene Expanded (Ex) was found accumulated at higher levels in the posterior compartment expressing GFP only ( Fig. 6A-A″). In contrast, a LacZ enhancer trap insertion into the shotgun gene (shg-LacZ), another Yki target 47 Table S4), with isoforms 2 and 3 from the NCBI gene database being pooled as identical transcripts by Ensembl (isoform DST-207). We therefore only consider DST-207, DST-202, DST-201 and DST-205. DST-207 and DST-202 contain the two CH, the plakin, the IF-BD, the EF-hand, the GAR domains and the spectrin-repeat rod (referred as BPAG1, Fig. 7A). In contrast, DST-201 contains the Plakin, the spectrin, the EF-hand and the GAR domains (referred to as BPAG1eA, Fig. 7A), while DST-205 encompasses the Plakin, the rod and the IF-BD domains (referred as BPAG1e, Fig. 7A). Searching through the ISOexpresso database (http://wiki.tgilab.org/ISOexpresso/) 48 , we found that BPAG1, BPAG1eA and BPAG1e were all expressed in normal breast tissues and were reduced by 29, 2.9 and 37 folds, respectively, in breast of surviving shLuc-or shDST-expressing MCF10A cells, treated with 250 nM of Doxorubicin. Data are from three biological replicates performed in triplicates. For all quantifications, error bars indicate SD.; *indicates P < 0.05; **indicates P < 0.005; ****indicates P < 0.0001.  www.nature.com/scientificreports www.nature.com/scientificreports/ tumour samples (Fig. 7B). We next examined if all DST isoforms were downregulated during transformation of the TAM-treated MCF10A-ER-Src cell line ( Fig. 1) using pairs of primers that specifically amplify BPAG1, BPAG1eA or BPAG1e. In contrast to the long BPAG1 isoforms, whose expression was not significantly altered during the 36 hours of TAM treatment (Fig. 7C), BPAG1eA and BPAG1e mRNA levels were reduced by 69% and 53%, starting 24 and 12 hours respectively after TAM treatment (Fig. 7D,E). These observations suggest that BPAG1eA and BPAG1e could function as the predominant DST tumour suppressor variants in breast epithelial cells.

BPAG1e and/or BPAG1eA prevent transformation in MCF10A cells.
To test if the downregulation of BPAG1e and BPAG1eA is sufficient to promote cellular transformation, we generated stable MCF10A cells carrying Tet-inducible shRNA against the BPAG1eA and BPAG1e isoforms (sh1eA/1e). Unlike shDST-expressing cells, which showed a reduction of all DST isoforms in both MCF10A-ER-Src and MCF10A cells ( Supplementary  Fig. S3), treating sh1eA/1e cells with Tet had no effect on BPAG1 mRNA levels, but reduced BPAG1eA and BPAG1e mRNA levels by 47% (Fig. 7F). Knocking down BPAG1eA and BPAG1e was sufficient to potentiate the colony-forming ability of MCF10A cells in clonogenic assays (Fig. 7G), as well as their mammosphere-forming capacity (Fig. 7H). Consistent with a role of BPAG1eA and/or BPAG1e as tumour suppressors in breast cells, www.nature.com/scientificreports www.nature.com/scientificreports/ MCF10A cells knocked down for BPAG1eA and BPAG1e using independent shRNA, displayed reduced BPAG1eA and BPAG1e mRNA expression specifically and formed higher number of mammospheres than control shLuc cells (Supplementary Fig. S3). Thus, BPAG1e and/or BPAG1eA prevent the acquisition of transformed features in MCF10A cells and could endorse most of DST tumour suppressive activity.  www.nature.com/scientificreports www.nature.com/scientificreports/ which involves mechanical signals controlled by the actin cytoskeleton, triggers YAP activity. Conversely, cell rounding and reduced adhesive area generated by softer substrates, cause cytoplasmic retention and YAP inhibition 22,23,50,51 . DST-depleted MCF10A cells, alike keratinocytes knocked down for BPAG1e 52 , exhibit reduced cell spreading and cell-substratum adhesion and fail to localize Paxillin and Vinculin at FAs. Thus, increased YAP activity in these cells unlikely results from higher cell-substrate tension. Still, DST could impact on YAP activity through the control of the actin cytoskeleton. This effect unlikely involves a direct control of F-actin by DST, as BPAG1e and BPAG1eA, the two DST variants that prevent transformation in MCF10A cells, do not contain the F-actin-binding calponin-homology domains. Instead, DST could affect F-actin by controlling actin-binding proteins. In agreement with this possibility, the activity of the actin-severing factor Cofilin is reduced in BPAG1edeficient keratinocytes 52,53 . As Cofilin restrains YAP activity in human cells and in Drosophila epithelia 22,54 , DST could limit YAP activity through Cofilin regulation. DST could also restrict YAP activity by keeping in check the actin-associated LIM domain protein Zyxin. We show that DST prevents Zyxin accumulation in MCF10A cells. In TAM-treated MCF10A-ER-Src, the downregulation of DST is also associated with the upregulation of Zyxin 34 . On possibility is that DST tethers Zyxin at FAs through maintaining FA integrity. In DST-depleted cells, Zyxin mislocalization could boost YAP activity, either through F-actin regulation, reminiscent to one of Zyxin's functions in Drosophila epithelia 26 and/or by stabilizing LATS 27,28 . According to the latter, DST-depleted MCF10A cells show reduced LATS protein levels. In support of a causal relationship between defective cell-substrate adhesion and impaired Hippo signalling, fibroblasts lacking the α-tubulin K40 acetyltransferase (αTat1), also display reduced number of FAs, impaired cell-substrate adhesion and fail to activate Hippo signalling upon cell-cell contacts 55 . Higher YAP activity due to the loss of DST could, in turn, initiate a positive feedback loop, which sustains its activity, as inhibiting YAP function in the triple-negative breast cancer cell line CAL51 upregulates DST and reduces Zyxin accumulation 51 .
A role for the BPAG1eA and/or BPAG1e DST isoforms in tumour suppression. Our observations suggest that the BPAG1eA and/or BPAG1e isoforms endorse the tumour suppressor function of DST. Consistent with this hypothesis, reducing all DST variants (shDST#2) or only BPAG1eA and BPAG1e by around 50%, potentiates to similar extends the colony-and mammosphere-forming abilities of MCF10A cells. Moreover, Src-induced transformation in MCF10A cells is associated with the downregulation of BPAG1eA and BPAG1e, but not with that of the long BPAG1 isoforms. How could BPAG1eA/BPAG1e impact on YAP activity? BPAG1eA contains a GAR microtubule-binding domain. Tao-1, known for destabilizing microtubules, controls Hippo pathway activity 56,57 . Moreover, acetylated microtubules by αTat1 have been proposed to regulate contact inhibition of proliferation through the Hippo pathway 55 . Thus, through its microtubule-binding activity, BPAG1eA could support FA and F-actin integrity, therein keeping in check YAP. Alternatively, the keratin-anchoring function of BPAG1e to the cell surface at the site of hemidesmosomes 58-63 could hold strong cell-matrix adhesions through FAs assembly and F-actin integrity. In agreement with this model, breast epithelial and myoepithelial cells assemble hemidesmosomes 64 . Moreover, hemidesmosomes can maintain the size of FAs 65 . Furthermore, carcinoma in situ and invasive breast cancer cells lack hemidesmosomes 64 . However, we cannot exclude that the long BPAG1 isoforms also exhibit tumour suppressor effects in breast epithelial cells, as all DST isoforms are downregulated in breast tumour samples. Moreover, knocking down all DST isoforms in EtOH-treated MCF10A-ER-Src cells has stronger effect on growth than TAM-treated MCF10A-ER-Src cells expressing shLuc.
DSt and cancer progression. Diverse observations suggest that the loss of DST could promote breast cancer progression irrespectively of the hormonal status. We show that DST has tumour suppressor activity in breast epithelial cells. Accordingly, DST has also been shown to prevent tumour growth and invasion in a MCF10ADCIS.com xenograft model 35 . Moreover, DST is downregulated in ER-positive DCIS and IDC and in ER-negative IDC. MCF10A cells with conditional Src induction also downregulate BPAG1eA and BPAG1e 33,34 . In addition, reducing further DST levels in these cells potentiates cell growth. The downregulation of DST in this inducible cell line could potentiate YAP activity, as the set of genes affected in TAM-treated MCF10A-ER-Src cells 34 show a significantly 5.31 folds enrichment (36/226 genes, p < 0.0001, Hypergeometric test) for YAP target genes in MCF10A cells 66 . In this model, which recapitulates the multistep process of Src-induced cellular transformation, cells transiently assemble stress fibres and FAs, leading to sustained cell proliferation 12 hours after induction. This state does not appear to involve YAP activation but depends on ERK and take place concomitantly to the downregulation of DST 33 . As reducing DST function in MCF10A cells affect FA integrity, the downregulation of DST in TAM-treated MCF10A-ER-Src cells could allow for FA and stress fibres disassembly after 12 hours of TAM treatment, consequently impeding Hippo pathway activity, and the progression towards a fully transformed state. Consistent with a role of Hippo signalling in breast cancer, LATS1 and LATS2 are downregulated in breast cancer and their depletion results in the acquisition of cancer-like features 67 . In contrast, high levels of Zyxin and nuclear YAP were reported in breast cancer tissues and both causes the acquisition of transformed features in breast cells 28,[68][69][70] . BPAG1e is also downregulated in nasopharyngeal carcinoma 71 . However, in invasive squamous cell carcinoma, BPAG1e is upregulated and confers cell migration, invasion and tumorigenic potential to oral squamous cell carcinoma cells 36,37 . Thus, in cancer cells, DST function could be context dependent. Consistent with this possibility, in the fly, while Shot restricts the overgrowth of wild type epithelia, it promotes growth in tissues overexpressing wts or knocked down for yki. Importantly, Zyxin also displays tissue-dependent opposite effects on cancer progression 72 . Thus, the tumour suppressor versus oncogenic roles of BPAG1e could rely upon Zyxin functions and interacting partners in distinct epithelia. However, we cannot exclude that distinct DST isoforms have opposite effects in cancer progression.
Taken together, our data demonstrate that the loss of DST in MCF10A cells triggers the acquisition of transformed features and potentiates YAP activity. Our observations are consistent with a model by which the tumour suppressor function of DST could be restricted to the shorter DST isoforms BPAG1eA and/or BPAG1e. As both . All cell lines were tested regularly for mycoplasma contamination and tested negative. After thawing, cell lines stably transfected with shLuc, shDST or shBPAG1eA/1e were cultured for two passages in media supplemented with 900 µg/ml of G418 (Thermo Fisher Scientific; 11811031).
Stable cell line generation. pLKO-TET-Neo vector containing shLuc, shDST or shBPAG1eA/1e were generated as described in Wiederschain et al. 73 . shRNA seed sequences were designed using Dharmacon siDesign Center (Supplementary Table S1). The pLKO-TET-Neo vector (Addgene, Watertown, MA, USA; Plasmid # 21916) was digested with ECoRI and AgeI, ligated with shRNA oligos and transformed into E.coli DH5alpha strain. Plasmids were purified using the WizardPlus Midiprep Kit (Promega, Madison, WI, USA; A7640) and transfected into HEK 293 T cells along with envelope and packaging plasmids using calcium phosphate transfection. Viral supernatants were collected 24 and 48 hours later, pooled together and used to infect MCF10A-pBABE-puro and MCF10A-ER-Src cells grown in media containing 8 µg/ml polybrene (Merck Millipore, Darmstadt, Germany; TR-1003-6) on two consecutive days. 48 hours post infection, cells were split and grown in media containing 900 µg/ml of G418 (Thermo Fisher Scientific, Waltham, MA, USA; 11811031) for selection. The levels of the housekeeping genes GAPDH, Actin and Histone H3 were compared by western blot between established stable cell lines and original cell lines to select for clones used in this study.

Drug treatments.
To determine the expression of DST in MCF10A-ER-Src cells, cells were seeded to reach 30% confluency 24 hours post-seeding and induced with 1 µM 4OH-TAM (Sigma-Aldrich, Darmstadt, Germany; H7904) or equal volume of EtOH in complete growth medium for the indicated time. To analyse the effect of reducing further DST in MCF10A-ER-Src-shLuc and MCF10A-ER-Src-shDST cells, cells were treated with 400 ng/ml Tet (Sigma-Aldrich; T7660) dissolved in 70% EtOH for 36 hours, 24 hours post-seeding, and treated with media containing 1 µM 4OH-TAM (Sigma-Aldrich; H7904) or an equal volume of EtOH for an additional 36 hours. To quantify the growth of MCF10A-ER-Src cells expressing shLuc or shDST, 3 000 cells per well in triplicates were seeded in 96 well plates for 24 hours and treated with Tet and TAM or EtOH as previously described. To analyse the effects of knocking down DST or BPAG1eA/1e in MCF10A cells, MCF10A-shLuc, MCF10A-shDST and MCF10A-shBPAG1eA/1e cells were seeded to reach 20% confluency after 24 hours and treated with 400 ng/ ml Tet in complete growth media for 72 hours. For testing the effect of knocking down DST on YAP sub-cellular localization and expression of its target genes, the number of MCF10A-shLuc and MCF10A-shDST cells seeded was determined to reach comparable percentage of cell confluency 72 hours after Tet treatment (Supplementary  Table S2). Cells were serum starved 12-14 hours before ending each experiment. For co-treatment with Tet and Verteporfin (VP), 40 000 cells per well were seeded in 24 well plates. After 24 hours, cells were pre-treated with 7.5 µM VP (Sigma-Aldrich; SML0534-5MG) or equivalent volume of DMSO in complete growth medium for 4 hours. Media was then replaced with media containing Tet and DMSO or VP for 24, 48 or 72 hours. For all experimental settings, media was changed every 24 hours.
MCF10A-shDST replicate treated with Tet for 72 hours and used to evaluate the expression of the YAP target genes CTGF, CYR61 and ITGB6 in Fig. 4B. Real-time pcR. Total RNA was isolated using the RNAeasy Kit (Qiagen, Hilden, Germany; 74104). 0.5 µg of purified RNA samples were used for first strand cDNA synthesis using random hexamer primers (Supplementary  Table S3 Identification of DST isoforms. DST/BPAG1 sequences were retrieved from the Ensembl database and NCBI. Primer-BLAST was used for designing isoform sequence primers (Supplementary Table S3). Current nomenclature for annotated isoforms and accession numbers are listed in Supplementary Table S4. fly Strains and Genetics. Fly stocks used were nub-Gal4 75 , hh-Gal4, agift from T. Tabata (University of Tokyo, Japan); tub-Gal80 ts ; UAS-Myc::wts 76 ; UAS-L(A)-GFP 77 , UAS-shot-RNAi GL01286 , shg k0340178 and UAS-yki-RNAi 4005R-2 (NIG-Fly). To analyse the effect of knocking down shot on the expression of Yki target genes, tub-Gal80 ts ; UAS-shot-RNAi GL01286 females were crosses with hh-Gal4, UAS-GFP males. Adults were left to lay eggs for 48 hours. Progeny were maintained at 18 °C for 6 days and switch to 25 °C until the end of third instar larvae. All other crosses were maintained at 25 °C. Larvae were dissected at the end of third instar. clonogenic assay. 500 MCF10A-shLuc or MCF10A-shDST or MCF10A-shDST#2 or MCF10-shBPAG1eA/1e cells treated with Tet for 72 hours were seeded per well in triplicates in 6 well plates and incubated for 9 days in complete growth media containing Tet. Media was replaced every 3 days. Colonies were then fixed with 3.5% paraformaldehyde and stained with 0.005% crystal violet dissolved in 20% ethanol solution. Colonies were counted manually. Colony forming efficiency (C.F.E.) was calculated as -(Number of colonies/Number of cells seeded) *100. Fold changes in C.F.E. were determined by normalizing to the C.F.E. of MCF10A-shLuc cells.
Drug resistance assay. To treat MCF10A-shLuc and MCF10A-shDST cells with Tet and Doxorubicin, cells were seeded to reach 20% confluency at 24 hours post-seeding and then treated with 400 ng/ml Tet (Sigma-Aldrich; T7660). After 48 hours, media containing 400 ng/ml Tet and 250 nM of Doxorubicin (Sigma-Aldrich; D1515) dissolved in PBS was applied for an additional 24 hours. 1 000 cells per well were then seeded in 6 well plates in triplicates and incubated for 9 days. Medium was replaced every 3 days with fresh media containing Tet. At the end of 9 days, colonies were fixed with 3.5% paraformaldehyde and stained with 0.005% crystal violet diluted in 20% ethanol solution. Colonies were counted manually. Percent surviving fraction was calculated as -(Number of colonies formed/Number of cells seeded*Plating Efficiency) 79  cell growth assay. The Cell Counting Kit-8 kit from Dojindo, Japan (277CK04-11) was used for determining relative cell number according to manufacturer's instructions. Cells were incubated for 2 hours with the CCK-8 reagent and the absorbance (optical density, O.D.) at 450 nm was detected using a Synergy Mx (BioTek, Vermont, USA) microplate reader. Absorbance was normalized to absorbance before treatment.
Luciferase reporter assay. 15 × 10 4 MCF10-shDST cells per well were seeded in 6 well plates, allowed to adhere for 24 hours and further grown for 24 hours in the presence or absence of Tet. Cells were then transiently transfected with 30 ng of pRL-TK plasmid and 720 ng of either pGL3-49 or pGL3-4XGTIIC-49 44 plasmid (A kindgift from Nic Tapon, The Francis Crick Institute) using Lipofectamine 2000 (Thermo Fisher Scientific; 11668019). Cells were then allowed to grow for 48 hours in complete growth media in the presence or absence of Tet, trypsinized and analyzed using the Dual Luciferase Reporter Kit (Promega, Madison, WI, USA; E1910) as per manufacturer's instructions. Luminescence was measured in triplicates for each sample on a Synergy Mx (BioTek) microplate reader. Relative luciferase activity was quantified by normalizing Firefly luciferase activity to their respective Renilla luciferase activity.
Immunofluorescence analysis and quantifications. For focal adhesion staining of MCF10A-shLuc and MCF10A-shDST, cells treated with Tet for 72 hours were trypzinized, reseeded on poly-L-lysine (Sigma-Aldrich; P8920) coated coverslips, allowed to attach and further grown for 48 hours in media containing Tet. For determining YAP sub-cellular localization, MCF10A-shLuc and MCF10A-shDST cells were seeded on poly-L-lysine coated coverslips, grown in complete growth media containing Tet for 72 hours and cells were serum starved for the last 12-14 hours before the end of each experiment. Cells were then fixed with 4% Formaldehyde solution in PBS at pH 7 for 10 minutes, permeabilized with 0.1% Triton X-100 and blocked with cytoskeletal binding buffer Blind quantifications of the percentages of cells with predominant nuclear YAP were performed separately by P. S. Guerreiro and F. Janody on 3 biological replicates by manual counting.
For wing imaginal discs of third instar larvae, staining were performed by dissecting larvae in phosphate buffer at pH 7 (0.1 M Na 2 HPO 4 , 0.1 M NaH 2 PO 4 at a 72:28 ratio). For analysing the effects of overexpressing wts or knocking down yki on the growth of nub > shot-RNAi-expressing wing discs, only female larvae were dissected. Samples were then fixed in 4% formaldehyde in PEM (0.1 M PIPES pH 7.0, 2 mM MgSO 4 , 1 mM EGTA) for 20 to 30 min, rinsed in phosphate buffer 0.2% Triton for 15 min and incubated with mouse anti-β-Galactosidase (1:200; Promega; Z37832000) or rabbit anti-Expanded (1/200; agift from A. Laughon, University of Wisconsin, Madison, WI, USA) or mouse anti-Discs large (1:50; Developmental Studies Hybridoma Bank, Iowa, USA, 4F3) overnight at 4 °C. Discs were then rinsed 3 times 10 min in phosphate buffer 0.2% triton, incubated for 1 h with TRITC-or Cy5-conjugated Donkey anti-mouse or anti-rabbit (Jackson ImmunoResearch) in phosphate buffer 0.2% triton supplemented with 10% horse serum. Samples were then rinsed 3 more times 10 min before being mounted in Vectashield. Fluorescence images were obtained on a Leica SP5 Live confocal microscope using a 10X (zoom twice) or 40X water objectives. The NIH Image J program was used to quantify wing disc area. Each disc was outlined and measured using the Area function, which evaluates size in square pixels. To quantify the ratio of the nub > GFP domain over the total wing disc area, the ratio between the area of the GFP domain and the area of the whole disc domain, measured using the Area function for each disc, were performed. cell-Substratum Adhesion Assay. 1.6 × 10 5 MCF10A-shLuc and MCF10A-shDST cells per well were seeded in 24 well plates in triplicates and incubated either in complete growth media or DMEM/F12 media without supplements for 16 hours. After removing media, wells were rinsed with ice-cold PBS ++ buffer (PBS containing 1 mM CaCl 2 and 1 mM MgCl 2 ), fixed with ice-cold methanol and incubated in 0.5% crystal violet dissolved in 20% ethanol for 20 minutes at room temperature. Excess crystal violet was discarded, cells were washed with PBS and incubated with methanol at room temperature to recover crystal violet from adherent cells. Absorbance at 590 nm was detected using a Synergy Mx (BioTek) microplate reader. Percentage of adhesion was calculated by considering adhesion in complete growth media as 100% as described in 80 . cell Spreading Assay. For measuring cell spreading, 5 000 MCF10A-shLuc and MCF10A-shDST cells were seeded per well in 24 well plates. Phase-contrast images were taken 6 hours post-seeding at 10X magnification. Cell area was determined using the Fiji software by detecting cell boundaries with the Find Edges function and acquiring cell area measurements with the Analyze Particles function. Statistical analysis. The Prism 7 (GraphPad Inc., San Diego, CA, USA) software was used for all statistical analysis. Unpaired t-test was used to compare two groups/treatments except for comparison of final cell number used to determine YAP target gene expression, where a paired t-test was used. For comparing alteration in total DST/BPAG1, BPAG1eA and BPAG1e mRNA levels in TAM-treated MCF10A-ER-Src cells, growth rates and distal wing disc area, multiple comparisons using one-way ANOVA were performed. p-values < 0.05 were considered to be significant. No statistical test was used to determine the number of biological replicates to be performed.

Data availability
All data and cell lines generated in this work are available upon request.