Department of Pathology and Immunology, Midwest Regional Center of Excellence for Biodefense and Emerging Infectious Diseases Research, Washington University School of Medicine, St Louis, MO 63110, USA.
Cell Host Microbe. 2010 Jun 25;7(6):516-26. doi: 10.1016/j.chom.2010.05.005.
Viral genetic studies typically focus on large open reading frames (ORFs) identified during genome annotation (ORF-based annotation). Here we describe tools for examining viral gene expression nucleotide by nucleotide across the genome. Using these tools on the 119,450 base pair (bp) genome of murine gammaherpesvirus 68 (gammaHV68) allowed us to establish that gammaHV68 RNA expression was significantly more complex than predicted from ORF-based annotation, including over 73,000 nucleotides of unexpected transcription within 30 expressed genomic regions (EGRs). Approximately 90% of this RNA expression was antisense to genomic regions containing known large ORFs. We verified the existence of previously undefined transcripts in three EGRs and determined which parts of the transcriptome depend on protein or viral DNA synthesis. This study redefines the genetic map of gammaHV68, indicating that herpesviruses contain significantly more genetic complexity than predicted from ORF-based genome annotations, and provides alternative tools and approaches for viral genetic studies.
病毒的遗传研究通常集中在基因组注释过程中确定的大型开放阅读框(ORF)上(基于 ORF 的注释)。在这里,我们描述了逐个核苷酸检查病毒基因表达的工具。在 119450 个碱基对(bp)的小鼠γ疱疹病毒 68(γHV68)基因组上使用这些工具,使我们能够确定γHV68 的 RNA 表达比基于 ORF 的注释预测的更为复杂,包括在 30 个表达基因组区域(EGR)内超过 73000 个核苷酸的意外转录。大约 90%的这种 RNA 表达与包含已知大型 ORF 的基因组区域呈反义。我们在三个 EGR 中验证了以前未定义的转录本的存在,并确定了转录组的哪些部分依赖于蛋白质或病毒 DNA 合成。这项研究重新定义了γHV68 的遗传图谱,表明疱疹病毒的遗传复杂性比基于 ORF 的基因组注释预测的要大得多,并为病毒的遗传研究提供了替代的工具和方法。