Moss B, Winters E, Cooper J A
J Virol. 1981 Nov;40(2):387-95. doi: 10.1128/JVI.40.2.387-395.1981.
Deletions contained within the genomes of unstable and stable variants of vaccinia virus (strain WR) were analyzed. Restriction endonuclease mapping and hybridization to specific 32P-labeled DNA probes indicated that more than 6 X 10(6) daltons of DNA were deleted from the variants. In each case, the deletion occurred on the left side of the genome and started very close to the junction of the inverted terminal repetition and unique sequence. Both variants also contained a new SstI side on the right side of the genome. Hybridization selection and cell-free translation experiments indicated that these variants lost the ability to synthesize at least eight early mRNA's mapping within the deleted region. Although the deleted DNA was not essential for replication of the WR strain of vaccinia virus under laboratory conditions of infection, it presumably has a defined role under other circumstances. This conclusion was based on the conservation within the Elstree strain of vaccinia, the Utrecht strain of rabbitpox, and the Brighton strain of cowpox virus of sequences homologous to the deleted DNA. Moreover, mRNA's that hybridized to the deleted vaccinia virus DNA segment and encoded similar size polypeptides were made in cells infected with rabbitpox and cowpox viruses.
对痘苗病毒(WR株)不稳定和稳定变异株基因组中的缺失情况进行了分析。限制性内切酶图谱分析以及与特定32P标记DNA探针的杂交表明,这些变异株缺失了超过6×10(6)道尔顿的DNA。在每种情况下,缺失都发生在基因组的左侧,且起始位置非常靠近反向末端重复序列与独特序列的交界处。这两种变异株在基因组右侧还都含有一个新的SstI位点。杂交筛选和无细胞翻译实验表明,这些变异株失去了合成至少8种定位于缺失区域内的早期mRNA的能力。虽然在实验室感染条件下,缺失的DNA对于痘苗病毒WR株的复制并非必不可少,但推测在其他情况下它具有特定作用。这一结论基于痘苗病毒埃尔斯特里株、兔痘病毒乌得勒支株以及牛痘病毒布莱顿株中与缺失DNA同源的序列的保守性。此外,在感染兔痘病毒和牛痘病毒的细胞中产生了与缺失的痘苗病毒DNA片段杂交并编码相似大小多肽的mRNA。