首页> 美国卫生研究院文献>Journal of Virology >The putative E5 open reading frame of cottontail rabbit papillomavirus is dispensable for papilloma formation in domestic rabbits.
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The putative E5 open reading frame of cottontail rabbit papillomavirus is dispensable for papilloma formation in domestic rabbits.

机译:棉尾兔乳头瘤病毒的推定的E5开放阅读框对于家兔乳头瘤的形成是必不可少的。

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摘要

In the cottontail rabbit papillomavirus (CRPV)-rabbit system, recombinant CRPV DNA can induce papillomas. This investigation was undertaken to evaluate whether the E5 open reading frame (ORF) of CRPV is required for papilloma formation. The CRPV genome we utilized, CRPV-WA, was sequenced in the E5 region and was found to contain one deletion, two insertions, and one transition mutation compared with CRPV-KS, the CRPV genome that has been fully sequenced. Despite these differences, an intact E5 ORF is preserved, supporting the notion that this gene may serve a biological function. One frameshift and two in-frame mutations were constructed in the small region of the 5' end of the E5 ORF that follows the E2 stop codon and precedes the L2 ORF. Several hundred rabbit skin sites were inoculated with each DNA preparation with a jet injector to test the ability of three CRPV E5 mutant DNAs to induce papillomas. In vivo results showed that each of the mutants induced papillomas, and biochemical analysis demonstrated that the E5 mutations present in DNA inocula were retained in the papillomas. The frequency of papilloma formation, however, was generally lower with each of the CRPV E5 mutants than with wild-type CRPV DNA, particularly so for the E5 frameshift mutant, suggesting that although the recognized E5 ORF is not required in domestic rabbits for the induction of papillomas by CRPV DNA, it may facilitate their formation.
机译:在棉尾兔乳头瘤病毒(CRPV)-兔子系统中,重组CRPV DNA可以诱导乳头状瘤。进行这项研究是为了评估乳头状瘤的形成是否需要CRPV的E5开放阅读框(ORF)。与CRPV-KS(已完全测序的CRPV基因组)相比,我们利用的CRPV基因组CRPV-WA在E5区进行了测序,发现包含一个缺失,两个插入和一个过渡突变。尽管存在这些差异,但仍保留了完整的E5 ORF,支持了该基因可能具有生物学功能的观念。在E5 ORF的5'末端的小区域中构建了一个移码和两个符合读框的突变,该小区域位于E2终止密码子之后且位于L2 ORF之前。用喷射注射器用每种DNA制剂接种数百只兔子皮肤部位,以测试三种CRPV E5突变体DNA诱导乳头状瘤的能力。体内结果表明,每个突变体均可诱导乳头状瘤,生化分析表明,DNA接种物中存在的E5突变保留在乳头状瘤中。然而,每个CRPV E5突变体的乳头状瘤形成频率通常低于野生型CRPV DNA,尤其是对于E5移码突变体,这表明尽管家兔中不需要公认的E5 ORF来诱导CRPV DNA对乳头状瘤的治疗,可能有助于它们的形成。

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