Department of Pathology, Georgetown University Medical School, 3900 Reservoir Road, NW, Washington, DC 20057, USA.
Biochem Biophys Res Commun. 2010 Sep 3;399(4):617-22. doi: 10.1016/j.bbrc.2010.07.125. Epub 2010 Aug 3.
The HPV-16 E5 protein resides in membranes of the endoplasmic reticulum (ER) and modulates cell growth and viral replication. In order to help define its biological activities, we analyzed E5-induced changes in human keratinocyte gene expression. Our studies identified the downregulation of spliced XBP-1 transcripts, a key player in the ER stress response, as a biochemical marker of E5 expression. IRE1alpha, the endoribonuclease responsible for XBP-1 RNA splicing, was also downregulated. Furthermore, cDNA microarray analysis revealed the repression of COX-2, another member of the ER stress pathway. In contrast, these genes were not altered either by the low-risk HPV-6b E5, or a C-terminal HPV-16 E5 mutant, in which the histidine and alanine residues (conserved in high-risk HPVs) were replaced with tyrosine and isoleucine (conserved in low-risk HPVs). HPV-16 E5 was also able to lower COX-2 mRNA levels in cells co-expressing E6/E7, suggesting that it might exert similar activity during viral replication. Interestingly, the E6/E7 genes were independently able to lower COX-2 transcripts compared to vector cells, indicating that multiple pathways of COX-2 repression exist. COX-2 downregulation by E5 could be overcome by thapsigargin or tunicamycin treatments, which initiate ER stress via calcium fluxes and abnormal protein glycosylation respectively, making it unlikely that E5 specifically tempers these pathways. Overall, our data indicate that E5 represses the cellular ER stress response and suggest a potential role for E5 during productive HPV infection.
HPV-16 E5 蛋白位于内质网(ER)的膜中,并调节细胞生长和病毒复制。为了帮助确定其生物学活性,我们分析了 E5 诱导的人角质形成细胞基因表达变化。我们的研究确定了剪接 XBP-1 转录本的下调,这是 ER 应激反应的关键参与者,作为 E5 表达的生化标记。IRE1alpha,负责 XBP-1 RNA 剪接的内切核酸酶,也被下调。此外,cDNA 微阵列分析显示 COX-2 的抑制,另一种 ER 应激途径的成员。相比之下,低风险 HPV-6b E5 或其中组氨酸和丙氨酸残基(在高危 HPV 中保守)被替换为酪氨酸和异亮氨酸(在低危 HPV 中保守)的 HPV-16 E5 突变体都没有改变这些基因。HPV-16 E5 还能够降低共表达 E6/E7 的细胞中的 COX-2 mRNA 水平,表明它在病毒复制过程中可能具有类似的活性。有趣的是,与载体细胞相比,E6/E7 基因能够独立地降低 COX-2 转录本,表明存在多种 COX-2 抑制途径。E5 对 COX-2 的下调可以被 thapsigargin 或 tunicamycin 处理克服,这分别通过钙通量和异常蛋白糖基化启动 ER 应激,因此不太可能是 E5 专门调节这些途径。总的来说,我们的数据表明 E5 抑制细胞 ER 应激反应,并表明 E5 在 HPV 感染过程中具有潜在作用。