| Literature DB >> 24074597 |
Jeremy Eberhard1, Zeynep Onder, Junona Moroianu.
Abstract
We previously discovered that nuclear import of high risk HPV16 E7 is mediated by a cNLS located within the zinc-binding domain via a pathway that is independent of karyopherins/importins (Angeline et al., 2003; Knapp et al., 2009). In this study we continued our characterization of the cNLS and nuclear import pathway of HPV16 E7. We find that an intact zinc-binding domain is essential for the cNLS function in mediating nuclear import of HPV16 E7. Mutagenesis of cysteine residues to alanine in each of the two CysXXCys motifs involved in zinc-binding changes the nuclear localization of the EGFP-16E7 and 2xEGFP-16E7 mutants. We further discover that a patch of hydrophobic residues, 65LRLCV69, within the zinc-binding domain of HPV16 E7 mediates its nuclear import via hydrophobic interactions with the FG domain of the central channel nucleoporin Nup62.Entities:
Keywords: EGFP; FG nucleoporin; GST; HPV; HPV16 E7 oncoprotein; Human papillomavirus; NES; NLS; NPC; Nuclear localization signal; 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: 24074597 PMCID: PMC3789256 DOI: 10.1016/j.virol.2013.08.017
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616