Angell S M, Baulcombe D C
The Sainsbury Laboratory, John Innes Centre, Colney, Norwich, UK.
EMBO J. 1997 Jun 16;16(12):3675-84. doi: 10.1093/emboj/16.12.3675.
Tobacco plants were transformed with constructs in which the transgene was a cDNA of replicating potato virus X (PVX) RNA. The constructs, referred to here as amplicons, were the intact genome of PVX and PVX constructs modified to carry the beta-glucuronidase (GUS) reporter gene either as an additional gene or as a replacement for the coat protein gene (PVX/GUS/CP and PVX/GUS respectively). Transformed plants carrying these constructs displayed several phenotypes that we attribute to post-transcriptional gene silencing. These phenotypes include the absence of viral symptoms, low accumulation of transgene-derived RNA, extreme strain-specific resistance against PVX, low and non-uniform GUS expression (in the PVX/GUS and PVX/GUS/CP plants) and suppression of transiently expressed RNA sharing homology with the transgene. Importantly, the amplicon-mediated gene silencing was exhibited in all lines tested. There was no evidence of gene silencing in seven lines expressing a PVX RNA that was unable to replicate. From these data we conclude that the replicating viral RNA is a potent trigger of gene silencing. Moreover, amplicon-mediated gene silencing provides an important new strategy for the consistent activation of gene silencing in transgenic plants.
将携带复制型马铃薯X病毒(PVX)RNA的cDNA作为转基因的构建体导入烟草植株。这里所说的构建体,即扩增子,是PVX的完整基因组以及经过修饰的PVX构建体,后者携带β-葡萄糖醛酸酶(GUS)报告基因,作为附加基因或替代外壳蛋白基因(分别为PVX/GUS/CP和PVX/GUS)。携带这些构建体的转基因植株表现出几种我们归因于转录后基因沉默的表型。这些表型包括无病毒症状、转基因衍生RNA积累量低、对PVX具有极端的株系特异性抗性、GUS表达低且不均匀(在PVX/GUS和PVX/GUS/CP植株中)以及与转基因具有同源性的瞬时表达RNA受到抑制。重要的是,在所有测试的株系中都表现出扩增子介导的基因沉默。在表达无法复制的PVX RNA的7个株系中没有基因沉默的证据。从这些数据我们得出结论,复制的病毒RNA是基因沉默的有效触发因素。此外,扩增子介导的基因沉默为在转基因植物中持续激活基因沉默提供了一种重要的新策略。