Qiu Wenping, Park Jong-Won, Scholthof Herman B
Department of Plant Pathology and Microbiology, Texas A&M University, College Station 77843-2132, USA.
Mol Plant Microbe Interact. 2002 Mar;15(3):269-80. doi: 10.1094/MPMI.2002.15.3.269.
The p19 protein (P19) of Tomato bushy stunt virus (TBSV) is a pathogenicity determinant with host-dependent effects on virus spread and symptom induction. In addition, results in this study confirm that Potato virus X-mediated delivery of P19 suppresses posttranscriptional gene silencing (PTGS). To study the relevance of this activity for TBSV biology, we evaluated whether TBSV activates virus-induced gene silencing (VIGS) and if this process is suppressed by P19. TBSV vectors with the green fluorescent protein (GFP) gene, either active or inactive for P19 expression, were inoculated onto GFP-transgenic Nicotiana benthamiana plants. In the absence of P19 expression, VIGS was activated, as evidenced by the disappearance of GFP mRNA and green fluorescence. Coexpression of GFP and P19 from the TBSV vector suppressed VIGS, except in the newly emerging leaves. The suppressor activity required a central P19 region that is also known to be essential for host-dependent virus spread and symptom induction. Defective interfering RNAs (DIs) that contained the 3' end of the GFP gene induced silencing very effectively. The concomitant DI-instigated reduction in P19 accumulation failed to suppress this process, analogous to the known P19 dosage effects for other biological activities. In conclusion, (i) TBSV and its DIs are very effective inducers of VIGS, (ii) P19 is a strong suppressor of PTGS, (iii) P19 is a moderate suppressor of VIGS, and (iv) the suppressor activity is influenced by genetic and dosage features that are also important for P19-associated pathogenesis.
番茄丛矮病毒(TBSV)的p19蛋白(P19)是一种致病性决定因子,对病毒传播和症状诱导具有宿主依赖性作用。此外,本研究结果证实,马铃薯X病毒介导的P19传递可抑制转录后基因沉默(PTGS)。为了研究这种活性与TBSV生物学的相关性,我们评估了TBSV是否激活病毒诱导的基因沉默(VIGS)以及该过程是否被P19抑制。将带有绿色荧光蛋白(GFP)基因且P19表达活性或无活性的TBSV载体接种到GFP转基因本氏烟草植株上。在没有P19表达的情况下,VIGS被激活,GFP mRNA和绿色荧光的消失证明了这一点。TBSV载体中GFP和P19的共表达抑制了VIGS,但新长出的叶子除外。抑制活性需要P19的一个中央区域,该区域也已知对宿主依赖性病毒传播和症状诱导至关重要。含有GFP基因3'端的缺陷干扰RNA(DIs)能非常有效地诱导沉默。与已知的P19对其他生物学活性的剂量效应类似,DIs引发的P19积累减少未能抑制这一过程。总之,(i)TBSV及其DIs是VIGS的非常有效的诱导剂,(ii)P19是PTGS的强抑制剂,(iii)P19是VIGS的中度抑制剂,(iv)抑制活性受遗传和剂量特征的影响,这些特征对与P19相关的发病机制也很重要。