Shade R O, Blundell M C, Cotmore S F, Tattersall P, Astell C R
J Virol. 1986 Jun;58(3):921-36. doi: 10.1128/JVI.58.3.921-936.1986.
The nucleotide sequence of an almost-full-length clone of human parvovirus B19 was determined. Whereas the extreme left and right ends of this genomic clone are incomplete, the sequence clearly indicates that the two ends of viral DNA are related by inverted terminal repeats similar to those of the Dependovirus genus. The coding regions are complete in the cloned DNA, and the two large open reading frames which span almost the entire genome are restricted to one strand, as has been found for all other parvoviruses characterized to date. From the DNA sequence we conclude that the organization of the B19 transcription units is similar although not identical to those of other parvoviruses. In particular, we predict that the B19 genome may utilize a fourth promoter to transcribe mRNA encoding the major structural polypeptide, VP2. Analysis of the putative polypeptides confirms that B19 is only distantly related to the other parvoviruses but reveals that there is a small region in the gene probably encoding the major nonstructural protein of B19, which is closely conserved between all of the parvovirus genomes for which sequence information is currently available.
测定了人细小病毒B19一个几乎全长克隆的核苷酸序列。虽然这个基因组克隆的最左端和最右端不完整,但序列清楚地表明病毒DNA的两端通过与腺联病毒属相似的反向末端重复序列相关。编码区在克隆的DNA中是完整的,并且跨越几乎整个基因组的两个大的开放阅读框局限于一条链,这与迄今所鉴定的所有其他细小病毒的情况相同。从DNA序列我们得出结论,B19转录单位的组织与其他细小病毒相似但不完全相同。特别是,我们预测B19基因组可能利用第四个启动子来转录编码主要结构多肽VP2的mRNA。对推定多肽的分析证实B19与其他细小病毒只有远缘关系,但揭示出在该基因中可能编码B19主要非结构蛋白的一个小区域,在目前有序列信息的所有细小病毒基因组之间是高度保守的。