Istituto di Virologia Vegetale, Consiglio Nazionale delle Ricerche, Strada delle Cacce 73, 10135, Turin, Italy.
Plant J. 2013 Sep;75(6):941-53. doi: 10.1111/tpj.12253. Epub 2013 Jul 20.
Tomato line 30.4 was obtained engineering the nucleocapsid (N) gene of tomato spotted wilt virus into plant genome, and immunity to tomato spotted wilt virus infection of its self-pollinated homozygous progeny was observed. Despite the presence of a high amount of transgenic transcripts, transgenic proteins have not been detected, suggesting a mechanism of resistance mediated by RNA. In the present study, we identify post-transcriptional gene silencing as the main mechanism of resistance, which is able to spread systemically through grafting, and show that the line 30.4 resistant plants produce both 24 and 21-22 nt N-gene specific siRNA classes. The transgenic locus in chromosome 4 shows complex multiple insertions of four T-DNA copies in various orientations, all with 3' end deletions in the terminator and part of the N gene. However, for three of them, polyadenylated transcripts are produced, due to flanking tomato genome sequences acting as alternative terminators. Interestingly, starting at the fifth generation after the transformation event, some individual plants show a tomato spotted wilt virus-susceptible phenotype. The change is associated with the disappearance of transgene-specific transcripts and siRNAs, and with hyper-methylation of the transgene, which proceeds gradually through the generations. Once it reaches a critical threshold, the shift from post-transcriptional gene silencing to transcriptional silencing of the transgene eliminates the previously well established virus resistance.
番茄品系 30.4 是通过将番茄斑萎病毒的核衣壳(N)基因工程转入植物基因组而获得的,观察到其自交纯合后代对番茄斑萎病毒感染具有免疫性。尽管存在大量的转基因转录本,但未检测到转基因蛋白,这表明存在 RNA 介导的抗性机制。在本研究中,我们确定了转录后基因沉默是主要的抗性机制,该机制能够通过嫁接在系统中传播,并表明品系 30.4 抗性植物产生了 24 个和 21-22nt 的 N 基因特异性 siRNA 类。4 号染色体上的转基因座标显示出复杂的四个 T-DNA 拷贝的多种插入,均具有终止子 3' 端缺失和部分 N 基因缺失。然而,由于侧翼番茄基因组序列充当替代终止子,其中三个拷贝产生了多聚腺苷酸化转录本。有趣的是,从转化事件后的第五代开始,一些个体植物表现出对番茄斑萎病毒的敏感性表型。这种变化与转基因特异性转录物和 siRNA 的消失以及转基因的超甲基化有关,随着世代的推移,超甲基化逐渐发生。一旦达到临界阈值,从转录后基因沉默到转基因的转录沉默的转变就会消除先前建立的良好的病毒抗性。