Prediction of a novel RNA binding domain in crocodilepox Zimbabwe Gene 157.

Nicole S Little, Taylor Quon, Chris Upton
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引用次数: 1

Abstract

Background: Although the crocodilepox virus (CRV) is currently unclassified, phylogenetic analyses suggest that its closest known relatives are molluscum contagiosum virus (MCV) and the avipox viruses. The CRV genome is approximately 190 kb and contains a large number of unique genes in addition to the set of conserved Chordopoxvirus genes found in all such viruses. Upon sequencing the viral genome, others noted that this virus was also unusual because of the lack of a series of common immuno-suppressive genes. However, the genome contains multiple genes of unknown function that are likely to function in reducing the anti-viral response of the host.

Results: By using sensitive database searches for similarity, we observed that gene 157 of CRV-strain Zimbabwe (CRV-ZWE) encodes a protein with a domain that is predicted to bind dsRNA. Domain characterization supported this prediction, therefore, we tested the ability of the Robetta protein structure prediction server to model the amino acid sequence of this protein on a well-characterized RNA binding domain. The model generated by Robetta suggests that CRV-ZWE-157 does indeed contain an RNA binding domain; the model could be overlaid on the template protein structure with high confidence.

Conclusion: We hypothesize that CRV-ZWE-157 encodes a novel poxvirus RNA binding protein and suggest that as a non-core gene it may play a role in host-range determination or function to dampen host anti-viral responses. Potential targets for this CRV protein include the host interferon response and miRNA pathways.

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鳄鱼津巴布韦基因157中一个新的RNA结合域的预测。
背景:虽然鳄鱼痘病毒(CRV)目前尚未分类,但系统发育分析表明,其已知的近亲是传染性软疣病毒(MCV)和禽痘病毒。CRV基因组约190 kb,除了在所有此类病毒中发现的一组保守的脊索虫病毒基因外,还包含大量独特的基因。在对病毒基因组进行测序后,其他人注意到这种病毒也不寻常,因为缺乏一系列常见的免疫抑制基因。然而,基因组包含多个功能未知的基因,这些基因可能在减少宿主的抗病毒反应中起作用。结果:通过使用敏感数据库搜索相似性,我们观察到crv -津巴布韦菌株(CRV-ZWE)的157基因编码一个具有预测结合dsRNA结构域的蛋白质。结构域表征支持这一预测,因此,我们测试了Robetta蛋白结构预测服务器在表征良好的RNA结合结构域上模拟该蛋白氨基酸序列的能力。Robetta建立的模型表明,CRV-ZWE-157确实含有RNA结合域;该模型可以高置信度地覆盖在模板蛋白结构上。结论:我们推测CRV-ZWE-157编码了一种新的痘病毒RNA结合蛋白,并提示作为一个非核心基因,它可能在宿主范围的决定或抑制宿主的抗病毒反应中发挥作用。该CRV蛋白的潜在靶点包括宿主干扰素反应和miRNA途径。
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