MacDowell S W, Coutts R H, Buck K W
Nucleic Acids Res. 1986 Oct 24;14(20):7967-84. doi: 10.1093/nar/14.20.7967.
A subgenomic single-stranded DNA present in particles of the geminivirus, tomato golden mosaic virus, has been shown by electron microscope heteroduplex mapping and Southern hybridisation analysis to consist of circular molecules, ca. 1.2 kb in size, derived from the smaller of the two genomic DNA components, DNA B, by deletion of open reading frame (ORF) BR1 and the C-terminal portion of ORF BL1. A covalently closed circular, supercoiled, double-stranded form of the subgenomic DNA has been isolated from virus-infected plants and cloned into pEMBL9. Analysis of the sequence of 22 clones across the deletion boundaries revealed only four different deletion boundaries, derived from four different left hand borders and three different right hand borders. Each border was within a region of 11 nucleotides and gave rise to a narrow size range (1248-1261 nucleotides) for the population of 22 subgenomic DNAs. However apparently smaller subgenomic DNAs were sometimes formed when plants were inoculated with cloned subgenomic DNA, or a construct derived from a subgenomic DNA in which a neomycin phosphotransferase gene had been inserted, together with the genomic DNA components. Mechanisms to account for the size, specificity and formation of the subgenomic DNA are discussed.
在双生病毒番茄金色花叶病毒颗粒中存在的一种亚基因组单链DNA,通过电子显微镜异源双链图谱分析和Southern杂交分析表明,它由环状分子组成,大小约为1.2 kb,是由两个基因组DNA组分中较小的DNA B通过缺失开放阅读框(ORF)BR1和ORF BL1的C末端部分而产生的。已从病毒感染的植物中分离出亚基因组DNA的共价闭合环状、超螺旋双链形式,并克隆到pEMBL9中。对跨越缺失边界的22个克隆的序列分析仅揭示了四个不同的缺失边界,分别来自四个不同的左手边界和三个不同的右手边界。每个边界都在11个核苷酸的区域内,使得22个亚基因组DNA群体的大小范围较窄(1248 - 1261个核苷酸)。然而,当用克隆的亚基因组DNA或插入了新霉素磷酸转移酶基因的亚基因组DNA衍生构建体与基因组DNA组分一起接种植物时,有时会形成明显较小的亚基因组DNA。文中讨论了解释亚基因组DNA大小、特异性和形成的机制。