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首页> 外文期刊>Virology >The full-length E1E4 protein of human papillomavirus type 18 modulates differentiation-dependent viral DNA amplification and late gene expression.
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The full-length E1E4 protein of human papillomavirus type 18 modulates differentiation-dependent viral DNA amplification and late gene expression.

机译:人类乳头瘤病毒18型的全长E1E4蛋白调节分化依赖性病毒DNA扩增和晚期基因表达。

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摘要

Activation of the productive phase of the human papillomavirus (HPV) life cycle in differentiated keratinocytes is coincident with high-level expression of E1E4 protein. To determine the role of E1E4 in the HPV replication cycle, we constructed HPV18 mutant genomes in which expression of the full-length E1E4 protein was abrogated. Undifferentiated keratinocytes containing mutant genomes showed enhanced proliferation when compared to cells containing wildtype genomes, but there were no differences in maintenance of viral episomes. Following differentiation, cells with mutant genomes exhibited reduced levels of viral DNA amplification and late gene expression, compared to wildtype genome-containing cells. This indicates that HPV18 E1E4 plays an important role in regulating HPV late functions, and it may also function in the early phase of the replication cycle. Our finding that full-length HPV18 E1E4 protein plays a significant role in promoting viral genome amplification concurs with a similar report with HPV31, but is in contrast to an HPV11 study where viral DNA amplification was not dependent on full-length E1E4 expression, and to HPV16 where only C-terminal truncations in E1E4 abrogated vegetative genome replication. This suggests that type-specific differences exist between various E1E4 proteins.
机译:在分化的角质形成细胞中激活人乳头瘤病毒(HPV)生命周期的生产期与E1E4蛋白的高水平表达相吻合。为了确定E1E4在HPV复制周期中的作用,我们构建了HPV18突变基因组,其中全长E1E4蛋白的表达被取消。与含有野生型基因组的细胞相比,含有突变基因组的未分化角质形成细胞显示出增强的增殖,但在维持病毒附加体方面没有差异。分化后,与含有野生型基因组的细胞相比,具有突变基因组的细胞显示出降低的病毒DNA扩增水平和晚期基因表达水平。这表明HPV18 E1E4在调节HPV的后期功能中起着重要作用,并且也可能在复制周期的早期起作用。我们的发现全长HPV18 E1E4蛋白在促进病毒基因组扩增中起着重要作用,这一点与HPV31的类似报道是一致的,但是与HPV11研究相反,在该研究中,病毒DNA扩增不依赖于全长E1E4表达,并且HPV16,其中E1E4中仅C端截短消除了营养基因组的复制。这表明各种E1E4蛋白之间存在类型特异性差异。

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