Petersen Birgit Otzen, Albrechtsen Merete
Biotechnology Group, Danish Institute of Agricultural Sciences, Thorvaldsensvej 40, DK-1871, Frederiksberg C, Denmark.
Plant Mol Biol. 2005 Jul;58(4):575-83. doi: 10.1007/s11103-005-7307-4.
RNA silencing is a sequence-specific RNA degradation mechanism found in most eukaryotes, where small cleavage products (siRNAs) of double stranded RNA (dsRNA) mediate silencing of genes with sequence identity to the dsRNA inducer. In several systems, silencing has been found to spread from the dsRNA inducer sequence into upstream or downstream regions of the target RNA, a phenomenon termed transitive silencing. In nematodes, silencing spreads only in the 3'-5' direction along the target mRNA by siRNAs serving as primers for cRNA synthesis by RNA-dependent RNA polymerase. In plants, transitive silencing is seen in both directions suggesting that at least some cRNA synthesis occurs by un-primed initiation at the 3' end of mRNAs. Replicating plant viruses trigger an RNA silencing defence response that degrades the viral RNA, thus tempering the virus infection. Likewise, fragments of plant genes inserted into a virus will become targets for degradation, leading to virus-induced gene silencing (VIGS) of the homologous plant mRNAs. We have analyzed the spreading of gene silencing in VIGS experiments using a transgene and two endogenous genes as targets. In Nicotiana benthamiana plants expressing a beta-glucuronidase (GUS) transgene, a Potato virus X vector carrying a 5' fragment of the GUS gene induced silencing which spread to downstream regions of the transgene mRNA including the 3'-untranslated region. Conversely, silencing induced by a 3' fragment spread only for a limited distance in the 3'-5' direction. Silencing induced by a central GUS gene fragment spread only into downstream regions. Similar analyses using the endogenous plant genes, magnesium chelatase subunit I (ChlI) and an RNase L inhibitor homologue (RLIh), revealed no spreading along target sequences. This implies that transitive silencing in plants occurs by un-primed cRNA synthesis from the 3' end of targeted (transgene) transcripts, and not by siRNA-primed cRNA synthesis.
RNA沉默是一种在大多数真核生物中发现的序列特异性RNA降解机制,其中双链RNA(dsRNA)的小切割产物(siRNAs)介导与dsRNA诱导物具有序列同一性的基因的沉默。在几个系统中,已发现沉默从dsRNA诱导物序列扩散到靶RNA的上游或下游区域,这种现象称为传递性沉默。在秀丽隐杆线虫中,沉默仅通过作为RNA依赖性RNA聚合酶合成cRNA引物的siRNAs沿靶mRNA在3'-5'方向上扩散。在植物中,在两个方向上都观察到传递性沉默,这表明至少一些cRNA合成是通过在mRNA的3'端进行无引物起始而发生的。复制性植物病毒引发RNA沉默防御反应,降解病毒RNA,从而减轻病毒感染。同样,插入病毒中的植物基因片段将成为降解的靶标,导致同源植物mRNA的病毒诱导基因沉默(VIGS)。我们在VIGS实验中使用转基因和两个内源基因作为靶标分析了基因沉默的扩散。在表达β-葡萄糖醛酸酶(GUS)转基因的本氏烟草植物中,携带GUS基因5'片段的马铃薯X病毒载体诱导了沉默,该沉默扩散到转基因mRNA的下游区域,包括3'-非翻译区。相反,由3'片段诱导的沉默仅在3'-5'方向上扩散有限的距离。由中央GUS基因片段诱导的沉默仅扩散到下游区域。使用内源植物基因镁螯合酶亚基I(ChlI)和RNase L抑制剂同源物(RLIh)进行的类似分析表明,沿靶序列没有扩散。这意味着植物中的传递性沉默是通过从靶向(转基因)转录本的3'端进行无引物cRNA合成而发生的,而不是通过siRNA引物的cRNA合成。