Journal of Virology · 2012 · 54 citations · 28 references
Life SciencesCancer BiologyMolecular BiologyCarcinogenesisMolecular OncologyMolecular VirologyHuman Papillomavirus InfectionOncogenic VirusesProtein DegradationProtein Interaction DomainsProtein TargetingStable Protein ComplexesE3 Ubiquitin Ligase Substrate RecognitionE6 OncoproteinHpv PathogenesisP53 InactivationPapillomavirus BiologyPeptide InteractionsRegulation By E3 Ubiquitin LigasesSubstrate Recognition In Ubiquitin Pathways
Human papillomavirus type 16 (HPV-16) E6 (16E6) binds the E3 ubiquitin ligase E6AP and p53, thereby targeting degradation of p53 (M. Scheffner, B. A. Werness, J. M. Huibregtse, A. J. Levine, and P. M. Howley, Cell 63:1129-1136, 1990). Here we show that minimal 16E6-binding LXXLL peptides reshape 16E6 to confer p53 interaction and stabilize 16E6 in vivo but that degradation of p53 by 16E6 requires E6AP expression. These experiments establish a general mechanism for how papillomavirus E6 binding to LXXLL peptides reshapes E6 to then act as an adapter molecule.
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Jiayuh Lin, Jiandong Chen, Brian Elenbaas et al. · Genes & Development · 1994 · 652 citations · Full text