Inverse Regulation of YAP and TAZ Functions by Tyrosine Phosphorylation/Dephosphorylation of Parafibromin
(A) HEK293T cells were transfected with indicated plasmids. TCLs were subjected to a sequential immunoprecipitation-immunoblotting analysis with indicated antibodies (left) and luciferase assay (right).
(B) HEK293T cells were transiently transfected with a TEAD luciferase reporter together with indicated plasmids. The cell lysates were subjected to luciferase assay.
(C) HEK293T cells were transfected with indicated plasmids. Anti-FLAG IP from cell lysates and TCL were subjected to immunoblotting with indicated antibodies.
(D) HEK293T cells were transiently transfected with a TEAD luciferase reporter together with indicated plasmids. The cell lysates were subjected to luciferase assay.
(E and F) HEK293T cells were transfected with indicated plasmids. TCLs and anti-FLAG immunoprecipitates from TCLs were subjected to immunoblotting with indicated antibodies.
Error bars, mean ± SD; n = 3; **p < 0.01 versus control vector (A and B), control vector with YAP2δ (D), or control vector with TAZ (D); ‡p < 0.01 versus PF with TAZ (A and D), or PF with YAP2δ (B).
See also Figure S6.