Nonnenmacher Mathieu, Salmon Jérôme, Jacob Yves, Orth Gérard, Breitburd Françoise
Unite des Papillomavirus, Institut Pasteur, 75724 Paris, Cedex 15, France.
J Virol. 2006 May;80(10):4890-900. doi: 10.1128/JVI.80.10.4890-4900.2006.
The cottontail rabbit papillomavirus (CRPV) a and b subtypes display a conserved E8 open reading frame encoding a 50-amino-acid hydrophobic protein, with structural similarities to the E5 transmembrane oncoprotein of genital human PVs (HPVs). CRPV E8 has been reported to play a role in papilloma growth but not to be essential in papilloma formation. Here we report that the knockout of E8 start codon almost prevented wart induction upon biobalistic inoculation of viral DNA onto rabbit skin. The scarce warts induced showed very slow growth, despite sustained expression of E6 and E7 oncogenes. This points to an essential role of E8 in disturbing epidermal homeostasis. Using a yeast two-hybrid screen, we found that E8 interacted with the zinc transporter ZnT1, protocadherin 1 (PCDH1), and AHNAK/desmoyokin, three proteins as yet unrelated to viral pathogenesis or cell transformation. HPV16 E5 also interacted with these proteins in two-hybrid assay. CRPV E8 mainly localized to the Golgi apparatus and the early endosomes of transfected keratinocytes and colocalized with ZnT1, PCDH1, and AHNAK. We showed that ZnT1 and PCDH1 formed a complex and that E8 disrupted this complex. CRPV E8, like HPV16 E5, increased epidermal growth factor (EGF)-dependent extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation and both the EGF-dependent and the EGF-independent activity of activating protein-1 (AP-1). Competition experiments with a nonfunctional truncated ZnT1 protein showed that E8-ZnT1 interaction was required for AP-1 activation. Our data identify CRPV E8 as a key player in papilloma induction and unravel novel cellular targets for inducing the proliferation of keratinocytes.
棉尾兔乳头瘤病毒(CRPV)的a和b亚型具有保守的E8开放阅读框,编码一种含50个氨基酸的疏水蛋白,其结构与生殖器人乳头瘤病毒(HPV)的E5跨膜癌蛋白相似。据报道,CRPV E8在乳头瘤生长中起作用,但对乳头瘤形成并非必不可少。在此我们报告,敲除E8起始密码子几乎可阻止通过生物弹道法将病毒DNA接种到兔皮肤上诱导疣的产生。尽管E6和E7癌基因持续表达,但诱导出的少量疣生长非常缓慢。这表明E8在扰乱表皮稳态中起关键作用。通过酵母双杂交筛选,我们发现E8与锌转运蛋白ZnT1、原钙黏蛋白1(PCDH1)和AHNAK/桥粒激酶相互作用,这三种蛋白与病毒发病机制或细胞转化尚无关联。在双杂交试验中,HPV16 E5也与这些蛋白相互作用。CRPV E8主要定位于转染角质形成细胞的高尔基体和早期内体,并与ZnT1、PCDH1和AHNAK共定位。我们发现ZnT1和PCDH1形成复合物,而E8破坏了该复合物。与HPV16 E5一样,CRPV E8增加了表皮生长因子(EGF)依赖性细胞外信号调节激酶1/2(ERK1/2)的磷酸化以及激活蛋白-1(AP-1)的EGF依赖性和EGF非依赖性活性。用无功能的截短ZnT1蛋白进行的竞争实验表明,E8与ZnT1的相互作用是AP-1激活所必需的。我们的数据确定CRPV E8是乳头瘤诱导中的关键因子,并揭示了诱导角质形成细胞增殖的新细胞靶点。