Chen J, Macfarlane S A, Wilson T M
Department of Virology, Scottish Crop Research Institute, Invergowrie, Dundee, United Kingdom.
Virology. 1995 May 10;209(1):213-7. doi: 10.1006/viro.1995.1245.
Plants mechanically inoculated with soil-borne wheat mosaic virus (SBWMV, Oklahoma isolate) generated several deleted forms of RNA2, the smaller genomic RNA (3593 nt). Four naturally deleted forms were cloned by RT-PCR methods and the sequences around each deletion site were compared. SBWMV RNA2 molecules were deleted for 519, 759, 964, or 1030 nt, respectively, each within the coat protein-readthrough domain. No common sequences were found flanking the 5'- and 3'-sites of deletion; however, the 5'-site of each deletion lay in the region between genome coordinates 1417-1465. The delta 759nt clone isolated from virus-infected plants after a single mechanical passage was identical to a clone described previously (J. Chen, S. A. MacFarlane, and T. M. A. Wilson, 1994, Virology 202, 921-929) which became the dominant, stable form of SBWMV RNA2 after five or more serial mechanical transfers. In this study, a total of 33 independent, RT-PCR clones with an apparent deletion of 759 nt, isolated after one to seven mechanical passages, were also sequenced and their precise deletion sites were compared. Twenty-six clones contained the original "stable," 759-nt deletion, whereas 7 clones, which were found only during the first four passages, had deletions at one of four alternative sites. After the fifth mechanical passage the stable 759-nt deletion dominated. The results also show that, in general, the smaller deletions are not intermediates in the larger deletion process. The complete nucleotide sequence of SBWMV RNA2 (Oklahoma) is also reported.
用土壤传播的小麦花叶病毒(SBWMV,俄克拉荷马分离株)进行机械接种的植物产生了几种RNA2的缺失形式,RNA2是较小的基因组RNA(3593个核苷酸)。通过RT-PCR方法克隆了四种天然缺失形式,并比较了每个缺失位点周围的序列。SBWMV RNA2分子分别缺失了519、759、964或1030个核苷酸,每个缺失都在衣壳蛋白通读结构域内。在缺失的5'和3'位点侧翼未发现共同序列;然而,每个缺失的5'位点位于基因组坐标1417 - 1465之间的区域。从病毒感染植物经单次机械传代后分离得到的缺失759个核苷酸的克隆与先前描述的一个克隆相同(J. Chen、S. A. MacFarlane和T. M. A. Wilson,1994年,《病毒学》202,921 - 929),该克隆在五次或更多次连续机械传代后成为SBWMV RNA2的主要稳定形式。在本研究中,还对总共33个独立的、经一至七次机械传代后分离得到的明显缺失759个核苷酸的RT-PCR克隆进行了测序,并比较了它们精确的缺失位点。26个克隆包含原始的“稳定”759个核苷酸缺失,而7个克隆(仅在前四次传代中发现)在四个替代位点之一有缺失。在第五次机械传代后,稳定的759个核苷酸缺失占主导。结果还表明,一般来说,较小的缺失不是较大缺失过程中的中间产物。还报道了SBWMV RNA2(俄克拉荷马)的完整核苷酸序列。