TEADs are the major TAZ binding transcription factors. A, SBP-TAZ is stably expressed in 293T cells. Retrovirus was used to establish SBP-TAZ stable cell clones. SBP-TAZ was purified with streptavidin-Sepharose, and the purified proteins were examined by Western blotting. B, silver staining for the streptavidin-Sepharose purified proteins. The streptavidin-Sepharose purified proteins were separated by SDS-PAGE for silver staining. C, identification of multiple TEAD peptides from TAZ immunocomplex. After SBP purification, trypsin digestion was performed on beads, and the total digestion mixture was directly analyzed by liquid chromatography-MS/MS. The identified peptides for each TEAD family member were shown. D, endogenous TEAD4 was coprecipitated by SBP-TAZ. Cell lysate was precipitated with SBP-Sepharose followed by Western blotting with antibodies against TAED4 and TAZ.

TEAD mediates TAZ-dependent gene induction. A, TAZ activates TEAD family transcription factors. 5× upstream activating sequence-Luciferase reporter, the indicated Gal4-fused transcription factors, and renilla were co-transfected with or without TAZ. The renilla activity normalized luciferase activity in the absence of TAZ was set to 1. B, Ser-51 of TAZ disrupts its interaction with TEAD4. The indicated plasmids were cotransfected into 293T cells. FLAG-TAZ was immunoprecipitated (IP) and probed with the indicated antibodies. C, TAZ^S51A loses the ability to activate TEAD4. The indicated plasmids were co-transfected with a 5× upstream activating sequence-luciferase reporter into 293T cells. Luciferase activity was measured and normalized to renilla activity. WT, wild type. D, dominant-negative TEAD1 blocks TAZ-mediated activation of CTGF promoter. The indicated plasmids were coexpressed in 293T cells. Cells were harvested for measurement of luciferase activity 24 h after transfection. E, TAZ binds to CTGF promoter. A ChIP assay was performed with anti-FLAG antibody using 293T cells stably expressing FLAG-TAZ. The presence of CTGF promoter was detected by PCR. WT, wild type. F, TEAD is required for TAZ-induced CTGF induction. RNA was extracted from the indicated MCF10A stable pools, and CTGF mRNA levels were analyzed by quantitative RT-PCR.

Disruption of TAZ-TEAD binding abolishes the function of TAZ in promoting cell proliferation. A, growth curve of MCF10A cells stably expressing wild-type or mutant TAZ as indicated. B, TAZ^4SA-S51A is compromised in inducing enlarged MCF10A cell acini. Indicated MCF10A-derived stable cells were cultured in three-dimensions on reconstituted basement membrane for 14 days before the pictures were taken. WT, wild type. C, growth curve of TAZ^4SA expressing MCF10A cells. TEAD1/3/4 knockdown by shRNA are indicated. D, TEAD knockdown inhibits MCF10A cell acinar growth. TAZ^4SA-expressing MCF10A cells were infected with control or TEAD1/3/4 shRNA lentivirus. Cell growth in Matrigel is shown.

Disruption of TEAD-TAZ binding blocks the ability of TAZ to promote EMT. A, S51A mutation in TAZ blocks TAZ induced EMT-like morphological change. Phase-contrast images of MCF10A cells stably expressing TAZ and its mutants are shown. B, Ser-51 mutation abolishes actin organization remodeling induced by TAZ. Cells were stained with rhodamine-conjugated phalloidin. C, Ser-51 mutation abolishes TAZ-induced EMT. Cell lysates from MCF10A cells stably expressing the wild-type (WT) and mutant TAZ were analyzed with the indicated epithelial and mesenchymal marker antibodies. D, Ser-51 mutation abolishes TAZ-induced change of E-cadherin and N-cadherin mRNA expression. Total RNA was extracted from MCF10A cells stably expressing the wild-type and mutant TAZ, and quantitative RT-PCR was employed to determine E-cadherin and N-cadherin mRNA levels. E, TEAD1/3/4 knockdown blocks TAZ-induced EMT-like morphological change. TEAD1/3/4 were knocked down by shRNA. Indicated MCF10A stable cells were cultured, and the pictures were taken.

TEAD is required for TAZ function in promoting cell migration. A, Ser-51 mutation abolishes TAZ-induced cell migration. Migration of MCF10A cells stably expressing the wild-type and mutant TAZ was determined by a wound-healing assay. B, TEAD1/3/4 knockdown blocks TAZ induced cell migration. Migration ability of indicated MCF10A stable cells was determined by a wound-healing assay.