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皮肤β属 HPV8 E7 癌蛋白的核输入是通过其锌结合域与 FG 核孔蛋白之间的疏水相互作用介导的。

Nuclear import of cutaneous beta genus HPV8 E7 oncoprotein is mediated by hydrophobic interactions between its zinc-binding domain and FG nucleoporins.

机构信息

Biology Department, Boston College, Chestnut Hill, MA 02467, USA.

Biology Department, Boston College, Chestnut Hill, MA 02467, USA.

出版信息

Virology. 2014 Jan 20;449:150-62. doi: 10.1016/j.virol.2013.11.020. Epub 2013 Dec 5.

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.

摘要

我们之前已经发现并描述了黏膜α 属 HPV 型 16 和 11 的 E7 癌蛋白的核输入途径。在这里,我们通过转染 EGFP-8E7 和突变质粒以及在离体细胞通透化的核输入测定中使用共聚焦显微镜,研究了皮肤β 属 HPV8 E7 蛋白的核输入。我们确定 HPV8 E7 在其锌结合域内含有一个核定位信号 (NLS),介导其核输入。此外,我们发现锌结合域内的一个主要疏水区 65LRLFV69 对于 HPV8 E7 的核输入和定位是必不可少的,这是通过与 FG 核孔蛋白 Nup62 和 Nup153 的疏水相互作用实现的。将疏水区 65LRLFV69 中的疏水残基突变为丙氨酸而不是 R66A 突变,会破坏 8E7 锌结合域与 Nup62 和 Nup153 之间的相互作用,从而抑制 HPV8 E7 的核输入。

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