Day A G, Bejarano E R, Buck K W, Burrell M, Lichtenstein C P
Centre for Biotechnology, Imperial College of Science, Technology and Medicine, London, United Kingdom.
Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6721-5. doi: 10.1073/pnas.88.15.6721.
Transgenic tobacco plants carrying a genetic cassette including an antisense DNA sequence of the virally encoded AL1 gene of the geminivirus tomato golden mosaic virus (TGMV) were constructed; AL1 encodes a protein absolutely required for TGMV DNA replication. These genetic cassettes also contained, on the same transcription unit, a gene encoding hygromycin resistance, which allowed selection for concomitant expression of the antisense gene. In transgenic lines, RNA transcripts of the predicted size and strand specificity were detected in antisense plants and sense controls. After infection of plants with TGMV, by agroinoculation, the frequency of symptom development was very significantly reduced in a number of antisense lines and correlated, broadly, with the abundance of antisense RNA transcript and with a reduction in viral DNA harvested from infected leaf tissue. We used an in vitro assay to study viral DNA replication in the absence of cell-to-cell spread; no replication was seen in five of the six antisense lines studied, in contrast to controls.
构建了携带遗传盒的转基因烟草植株,该遗传盒包含双生病毒番茄金色花叶病毒(TGMV)病毒编码的AL1基因的反义DNA序列;AL1编码TGMV DNA复制绝对必需的一种蛋白质。这些遗传盒在同一转录单元上还包含一个编码潮霉素抗性的基因,这使得能够选择反义基因的伴随表达。在转基因株系中,在反义植株和正义对照中检测到了预测大小和链特异性的RNA转录本。通过农杆菌接种用TGMV感染植物后,许多反义株系中症状出现的频率显著降低,并且大致与反义RNA转录本的丰度以及从感染叶组织中收获的病毒DNA的减少相关。我们使用体外试验来研究在不存在细胞间传播的情况下病毒DNA的复制;与对照相比,在所研究的六个反义株系中的五个中未观察到复制。