
Regulation of DeltaNp63alpha can be achieved at the transcriptional and post-translational levels, with the latter being greatly influenced by external stimuli such as DNA damaging agents. In this present study, we demonstrated that DeltaNp63alpha physical interacts with Yes-associated protein 1 (Yap1). Ectopic expression of Yap1 decreased the stability and the half-like of DeltaNp63alpha and resulted in ubiquitin-dependent degradation of DeltaNp63alpha. Further, the cisplatin mediated degradation of DeltaNp63alpha is attenuated with the downregulation of Yap1. Thus, our results strongly suggest that Yap1 plays a role in the regulation of endogenous DeltaNp63alpha levels and is likely to contribute to the regulation of DeltaNp63alpha, in physiological conditions.
Protein Stability, Tumor Suppressor Proteins, Blotting, Western, Apoptosis, YAP-Signaling Proteins, Phosphoproteins, Cell Line, Tumor, Trans-Activators, Humans, Immunoprecipitation, Adaptor Proteins, Signal Transducing, Protein Binding, Transcription Factors
Protein Stability, Tumor Suppressor Proteins, Blotting, Western, Apoptosis, YAP-Signaling Proteins, Phosphoproteins, Cell Line, Tumor, Trans-Activators, Humans, Immunoprecipitation, Adaptor Proteins, Signal Transducing, Protein Binding, Transcription Factors
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
