Blissard G W, Smith O P, Summers M D
Virology. 1987 Sep;160(1):120-34. doi: 10.1016/0042-6822(87)90052-3.
Campoletis sonorensis virus (CsV) (Polydnaviridae) is a large eucaryotic DNA virus with a structurally complex genome consisting of 28 or more superhelical (SH) DNA segments. Little is known of the relationship between different SH DNAs, but some SH DNAs do cross hybridize, indicating a relatedness between certain SH DNAs. In a previous study of viral expression in parasitized Heliothis virescens larvae, several partially homologous viral mRNAs were also identified (G. W. Blissard, S. B. Vinson, and M. D. Summers, 1986, J. Virol. 57, 318-327). To study the organization of the viral genome and the relationship between two partially homologous viral mRNAs, we analyzed cDNA clones and a cloned SH DNA segment of the CsV genome. Of the two CsV mRNAs examined (1.6 and 1.0 kb), both mRNAs were abundant at 48 hr after parasitization and the 1.6-kb mRNA was detected as early as 2 hr after parasitization. Nucleotide sequence analyses of cDNA clones representing the two partially homologous CsV mRNAs (1.6 and 1.0 kb) show that the two CsV mRNAs share five regions of imperfect homology (68 to 88%) which include a large part of each mRNA. These data indicate that the two mRNAs are transcribed from two separate but closely related CsV genes. Comparison of predicted amino acid sequences shows that the two related viral genes encode proteins with divergent amino acid sequences. Northern and Southern hybridization analyses using cloned cDNAs as probes showed that one CsV mRNA (1.6 kb) is homologous to CsV SH DNAs W, R, and M, while the other mRNA (1.0 kb) shows strong homology only to SH DNA W. By cloning and Southern hybridization mapping of the 15.8-kbp SH DNA W, we demonstrate that the genes for the related 1.6- and 1.0-kb mRNAs are located on different regions of this single 15.8-kbp SH DNA. Alignment of nucleotide sequences from a cloned viral genomic DNA and a cDNA demonstrates that the CsV gene encoding the 1.6-kb mRNA is a spliced gene containing at least two introns. Conservation of splice junctions between the two mRNAs suggests that the 1.0-kb mRNA is also spliced. These data represent the detailed analysis of two closely related CsV mRNAs abundantly expressed in parasitized H. virescens larvae, the first observation of related viral genes in a eucaryotic DNA virus, the demonstration of splicing in the Polydnaviridae, and the cloning and mapping of one of the largest SH DNA segments of the CsV genome.
桑蚕饰腹寄蝇病毒(CsV)(多DNA病毒科)是一种大型真核DNA病毒,其基因组结构复杂,由28个或更多超螺旋(SH)DNA片段组成。对于不同SH DNA之间的关系了解甚少,但一些SH DNA确实会交叉杂交,这表明某些SH DNA之间存在相关性。在之前一项关于寄生的烟草天蛾幼虫中病毒表达的研究中,还鉴定出了几种部分同源的病毒mRNA(G. W. 布利萨德、S. B. 文森和M. D. 萨默斯,1986年,《病毒学杂志》57卷,318 - 327页)。为了研究病毒基因组的组织以及两种部分同源病毒mRNA之间的关系,我们分析了CsV基因组的cDNA克隆和一个克隆的SH DNA片段。在所检测的两种CsV mRNA(1.6 kb和1.0 kb)中,两种mRNA在寄生后48小时都很丰富,并且1.6 kb的mRNA在寄生后2小时就被检测到。对代表两种部分同源CsV mRNA(1.6 kb和1.0 kb)的cDNA克隆进行核苷酸序列分析表明,这两种CsV mRNA共有五个不完全同源的区域(68%至88%),其中包括每种mRNA的大部分。这些数据表明这两种mRNA是从两个不同但密切相关的CsV基因转录而来的。预测氨基酸序列的比较表明,这两个相关的病毒基因编码的蛋白质具有不同的氨基酸序列。使用克隆的cDNA作为探针进行的Northern和Southern杂交分析表明,一种CsV mRNA(1.6 kb)与CsV SH DNA W、R和M同源,而另一种mRNA(1.0 kb)仅与SH DNA W有很强的同源性。通过对15.8 kbp的SH DNA W进行克隆和Southern杂交图谱分析,我们证明了与1.6 kb和1.0 kb相关mRNA的基因位于这个单一的15.8 kbp SH DNA的不同区域。克隆的病毒基因组DNA和cDNA的核苷酸序列比对表明,编码1.6 kb mRNA的CsV基因是一个剪接基因,至少包含两个内含子。两种mRNA之间剪接位点的保守性表明1.0 kb的mRNA也是剪接的。这些数据代表了对在寄生的烟草天蛾幼虫中大量表达的两种密切相关的CsV mRNA的详细分析,首次观察到真核DNA病毒中的相关病毒基因,多DNA病毒科中剪接的证明,以及CsV基因组最大的SH DNA片段之一的克隆和图谱分析。