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. 2022 Mar 12;13(3):231. doi: 10.1038/s41419-022-04675-2

Fig. 1. Fbxo45 negatively regulates USP49 stability through ubiquitinated degradation.

Fig. 1

A IB analysis of whole-cell lysates (WCLs) derived from Panc-1 cells transfected with the indicated plasmids, which were treated with 10 μM MG132 for 6 h before harvesting. B IB analysis of WCLs derived from Panc-1 cells transfected with Fbxo45 constructs or EV. EV: empty vector. C IB analysis of WCLs derived from Panc-1 cells transfected with Fbxo45 siRNA or the negative control (NC). D qRT-PCR analysis to detect Fbxo45 and USP49 mRNA levels after Fbxo45 depletion in 293 T cells. Data are shown as the mean ± SD of three independent experiments. ***p < 0.001 compared to NC. E IB analysis of WCLs derived from Panc-1 cells after the specified duration of 100 μg/ml cycloheximide (CHX) transfection with Fbxo45 siRNA. F USP49 protein abundance in (E) was quantified and plotted. G IB analysis of immunoprecipitates (IPs) and WCLs derived from Panc-1 cells transfected with the indicated plasmids. Cells were treated with 10 μM MG132 for 6 h before harvesting. H IB analysis of ubiquitination products and WCLs derived from Panc-1 cells transfected with the indicated constructs. Cells were treated with 10 μM MG132 for 6 h before harvesting.