| Literature DB >> 24418548 |
Zeynep Onder1, Junona Moroianu2.
Abstract
We have previously discovered and characterized the nuclear import pathways for the E7 oncoproteins of mucosal alpha genus HPVs, type 16 and 11. Here we investigated the nuclear import of cutaneous beta genus HPV8 E7 protein using confocal microscopy after transfections of HeLa cells with EGFP-8E7 and mutant plasmids and nuclear import assays in digitonin-permeabilized HeLa cells. We determined that HPV8 E7 contains a nuclear localization signal (NLS) within its zinc-binding domain that mediates its nuclear import. Furthermore, we discovered that a mostly hydrophobic patch 65LRLFV69 within the zinc-binding domain is essential for the nuclear import and localization of HPV8 E7 via hydrophobic interactions with the FG nucleoporins Nup62 and Nup153. Substitution of the hydrophobic residues within the 65LRLFV69 patch to alanines, and not R66A mutation, disrupt the interactions between the 8E7 zinc-binding domain and Nup62 and Nup153 and consequently inhibit nuclear import of HPV8 E7.Entities:
Keywords: Beta genus human papillomaviruses; EGFP; FG nucleoporins; GST; HPV; HPV8 E7 oncoprotein; NES; NLS; NPC; Nuclear localization signal; Nup153; Nup62; enhanced green fluorescent protein; glutathione-S-transferase; human papillomavirus; nuclear export signal; nuclear localization signal; nuclear pore complex
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Year: 2013 PMID: 24418548 PMCID: PMC3894589 DOI: 10.1016/j.virol.2013.11.020
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616