HCV:写在我们的DNA里。

Darja Kanduc
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引用次数: 8

摘要

对丙型肝炎病毒(HCV)多蛋白和人类蛋白质之间序列相似性的检查显示,多肽共享程度很高,病毒特有的基序数量有限(即,在人类蛋白质组中没有对应的基序)。使用五肽匹配,在总共3,007个基序中,只有214个基序(7.11%)与智人蛋白质组相比鉴定出HCV为非己基序。然而,这种病毒与人类的表型差异在遗传水平上消失了。事实上,一项针对HCV特有的214个五肽的五聚体寡脱氧核苷酸序列的BLAST分析显示,几乎所有这些序列都存在于人类基因组中,位于非编码链、内含子和/或假基因中,因此是不可翻译的。目前的数据警告不要使用基于dna的疫苗来对抗HCV感染,并强调肽的独特性是设计有效的抗HCV免疫治疗方法的分子基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HCV: Written in our DNA.

An inspection of the sequence similarity between the hepatitis C virus (HCV) polyprotein and human proteins revealed a high level of peptide sharing, with a limited number of motifs unique to the virus (i.e., with no counterpart in the human proteome). Using pentapeptide matching, only 214 motifs out of a total of 3,007 (7.11%) identified HCV as nonself compared to the Homo sapiens proteome. However, this virus-versus-human phenetic difference disappeared at the genetic level. Indeed, a BLAST analysis of pentadecameric oligodeoxynucleotide sequences corresponding to the 214 pentapeptides unique to HCV revealed that almost all of them are present in the human genome, located in the non-coding strand, introns, and/or pseudogenes, thus being, as such, untranslatable. The present data warn against using DNA-based vaccines to fight HCV infection and emphasize peptide uniqueness as the molecular basis for designing effective anti-HCV immunotherapeutic approaches.

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