Biology Department, Boston College, Chestnut Hill, MA 02467, USA.
Virology. 2013 Nov;446(1-2):334-45. doi: 10.1016/j.virol.2013.08.017. Epub 2013 Sep 10.
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.
我们之前发现高危型 HPV16 E7 的核输入是通过锌结合域内的一个 cNLS 介导的,该途径不依赖于核孔蛋白/输入蛋白 (Angeline 等人,2003 年;Knapp 等人,2009 年)。在这项研究中,我们继续对 HPV16 E7 的 cNLS 和核输入途径进行了表征。我们发现,完整的锌结合域对于 cNLS 介导 HPV16 E7 的核输入是必不可少的。在参与锌结合的两个 CysXXCys 基序中的每个半胱氨酸残基突变为丙氨酸,会改变 EGFP-16E7 和 2xEGFP-16E7 突变体的核定位。我们进一步发现,HPV16 E7 的锌结合域内的一个疏水性残基簇 65LRLCV69 通过与中央通道核孔蛋白 Nup62 的 FG 结构域的疏水相互作用来介导其核输入。