Jakab G, Droz E, Brigneti G, Baulcombe D, Malnoë P
Station Fédérale de Recherches en Production Végétale de Changins, Nyon, Switzerland.
J Gen Virol. 1997 Dec;78 ( Pt 12):3141-5. doi: 10.1099/0022-1317-78-12-3141.
A full-length cDNA clone of the potato virus Y (PVY) genome was obtained after cloning difficulties in Escherichia coli were overcome. These difficulties were mainly due to the expression of the CI gene from upstream prokaryotic promoter-like elements within the PVY genome. To overcome this problem, PVY cDNA was maintained in two subclones which were ligated before infection. A plasmid in which these two fragments were contained could be propagated in some E. coli strains but was unstable and yielded only low levels of plasmid DNA. Replacement of the 35S promoter by the SP6 promoter slightly increased the stability of the plasmid and its RNA transcripts were infectious when capped with m7G(5')ppp(5')G. Using two inoculation methods (mechanical or biolistic) the cDNA and its RNA transcript proved infectious on three Nicotiana species and on Solanum tuberosum.
克服了在大肠杆菌中克隆的困难后,获得了马铃薯Y病毒(PVY)基因组的全长cDNA克隆。这些困难主要是由于PVY基因组内上游原核启动子样元件对CI基因的表达所致。为克服这一问题,PVY cDNA保存在两个亚克隆中,在感染前将它们连接起来。含有这两个片段的质粒可在一些大肠杆菌菌株中繁殖,但不稳定,质粒DNA产量很低。用SP6启动子取代35S启动子可略微提高质粒的稳定性,其RNA转录本在加上m7G(5')ppp(5')G帽后具有感染性。使用两种接种方法(机械接种或基因枪接种),cDNA及其RNA转录本在三种烟草属植物和马铃薯上均被证明具有感染性。