应用生物信息学工具研究犬疱疹病毒1型(CHV-1)基因组中与潜伏相关转录的DNA序列

Ortiz M. A. Hern aacute, ndez, Verde C. Cuenca, L. Valdivia, Anda G. Valdivia
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引用次数: 2

摘要

疱疹病毒的一个共同特征是能够在宿主中建立潜伏感染,在潜伏期检测到一个转录活跃区域以及一组被称为潜伏期相关转录本(LATs)的RNA,它们的功能在最近的工作中得到了阐明。为了确定犬1型疱疹病毒(CHV-1)是否有一个与潜伏期相关的区域,本研究采用了不同的生物信息学方法。我们的结果是选择了9个miRNA候选序列(MIREval 2.0软件),26个miRNA (miRNAFold v.1.0软件),其中14个具有真正的miRNA前体,2个在RL2和RS1基因之间,1个在RL2基因中,11个在RS1基因中。结果表明,在分析的疱疹病毒中,这些区域的相似性非常低,因此无法用生物信息学推断犬疱疹病毒1型中是否存在LAT基因。另一方面,比较表明预测的miRNA: chv1-mir- mirnafoil -8与eb病毒(EBV)的EBV -mir- bart7 -3p具有相似性,因此通过生物信息学程序预测的miRNA符合这些分子的理论要求,但由于在其他疱疹病毒中没有一定程度的保存,因此CHV-1在潜伏期的表达无法确定,需要通过实验测试进行鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of DNA Sequences Related to Latency-Associated Transcripts in the Genome of Canine Herpesvirus Type 1 (CHV-1) by Means of Bioinformatics Tools
A characteristic common to herpesviruses is the ability to establish a latent infection in the hosts, a transcriptionally active region has detected during latency as well as a set of RNA that are known as Latency Associated Transcripts (LATs), their functions have been clarified in recent work. The present work was carried using different bioinformatics method in order to determine if Herpesvirus Canine 1 (CHV-1) has a region associated with latency. Our result was the selection of nine sequences candidate of micro RNA (miRNA) (MIREval 2.0 software), and 26 miRNA (miRNAFold v.1.0 software), of them, were selected 14 with real precursors of miRNA, two were found between the RL2 and RS1 genes, one in the RL2 gene and 11 in the RS1 gene. The results showed that the similarities of these regions are very low among the herpesviruses analyzed, so it was not possible to deduce the presence of the LAT gene in canine herpesvirus type 1 with bioinformatics. On the other hand, the comparison showed that the miRNA predicted: chv1-mir-mirnafold-8 has similarity with the ebv-mir-BART7-3p of Epstein-Barr Virus (EBV), in this way, the microRNAs predicted by means of bioinformatic programs met the theoretical requirements of these molecules, however at not having a degree of preservation in other herpesviruses, the expression by CHV-1 in latency cannot be confirmed and it is necessary to identify through experimental tests.
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