Abstract

AbstractThe high-risk human papillomavirus (HPV) E6 proteins stimulate the ubiquitination and degradation of p53, dependent on the E6AP ubiquitin-protein ligase. Other proteins have also been shown to be targeted for degradation by E6, including hDlg, the human homolog of the Drosophila melanogaster Discs large (Dlg) tumor suppressor. We show here that the human homolog of the Drosophila Scribble (Vartul) (hScrib) tumor suppressor protein is also targeted for ubiquitination by the E6-E6AP complex in vitro and that expression of E6 induces degradation of hScrib in vivo. Characterization of the E6AP-E6-hScrib complex indicated that hScrib binds directly to E6 and that the binding is mediated by the PDZ domains of hScrib and a carboxyl-terminal epitope conserved among the high-risk HPV E6 proteins. Green fluorescent protein-hScrib was localized to the periphery of MDCK cells, where it colocalized with ZO-1, a component of tight junctions. E6 expression resulted in loss of integrity of tight junctions, as measured by ZO-1 localization, and this effect was dependent on the PDZ binding epitope of E6. Thus, the high-risk HPV E6 proteins induce the degradation of the human homologs of two Drosophila PDZ domain-containing tumor suppressor proteins, hDlg and hScrib, both of which are associated with cell junction complexes. The fact that Scrib/Vart and Dlg appear to cooperate in a pathway that controls Drosophila epithelial cell growth suggests that the combined targeting of hScrib and hDlg is an important component of the biologic activity of high-risk HPV E6 proteins. ACKNOWLEDGMENTSThis work was supported by a grant to J.M.H. from the National Institutes of Health (CA72943), and S.N. was supported by a fellowship from the University of Tokyo, Faculty of Medicine, and the Kanzawa Medical Research Foundation.We thank Bernard Mechler for communication of unpublished results, members of our laboratory for helpful discussions, Sylvie Beaudenon for generation and characterization of HPV39 E6 baculovirus, the Kazusa DNA Research Institute, Chiba, Japan, for providing cDNA for KIAA0147, and Go Totsukawa, Fumio Matsumura, and Herb Geller and the Robert Wood Johnson Medical School Confocal and Electronic Imaging Center for assistance with microscopy and image analysis.