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. 2013 Nov 25;110(50):E4849–E4857. doi: 10.1073/pnas.1319656110

Fig. 3.

Fig. 3.

Expression of Cep192 DN80 or Cep152 DN217 is sufficient to alter subcellular localization of Plk4. (A) 293T cells transfected with the indicated constructs were subjected to GST pull-down assays. Arrowheads mark endogenous Plk4 coprecipitated with GST-DN80 or GST-DN217, but not with their respective 2A mutant or control GST (not shown because of small molecular size). (B and C) U2OS cells stably expressing the indicated GFP-DN80 or GFP-DN217 constructs were subjected to immunoblotting analyses (B) using antibodies that detect the epitope commonly present in the GFP-fused form and its respective endogenous protein. The cells were also immunostained (C) to determine the level of Plk4 at the centrosomes. Asterisks in (B) mark nonspecific cross-reacting proteins.