Key Laboratory of Forage and Endemic Crop Biotechnology, Ministry of Education, School of Life Sciences, Inner Mongolia University, Hohhot 010070, P. R. China.
Plant Physiol. 2021 Mar 15;185(2):424-440. doi: 10.1093/plphys/kiaa018.
Orobanche cumana is a holoparasitic plant that attaches to host-plant roots and seriously reduces the yield of sunflower (Helianthus annuus L.). Effective control methods are lacking with only a few known sources of genetic resistance. In this study, a seed-soak agroinoculation (SSA) method was established, and recombinant tobacco rattle virus vectors were constructed to express RNA interference (RNAi) inducers to cause virus-induced gene silencing (VIGS) in sunflower. A host target gene HaTubulin was systemically silenced in both leaf and root tissues by the SSA-VIGS approach. Trans-species silencing of O. cumana genes were confirmed for 10 out of 11 target genes with silencing efficiency of 23.43%-92.67%. Knockdown of target OcQR1, OcCKX5, and OcWRI1 genes reduced the haustoria number, and silencing of OcEXPA6 caused further phenotypic abnormalities such as shorter tubercles and necrosis. Overexpression of OcEXPA6 caused retarded root growth in alfalfa (Medicago sativa). The results demonstrate that these genes play an important role in the processes of O. cumana parasitism. High-throughput small RNA (sRNA) sequencing and bioinformatics analyses unveiled the distinct features of target gene-derived siRNAs in O. cumana such as siRNA transitivity, strand polarity, hotspot region, and 21/22-nt siRNA predominance, the latter of which was confirmed by Northern blot experiments. The possible RNAi mechanism is also discussed by analyzing RNAi machinery genes in O. cumana. Taken together, we established an efficient host-induced gene silencing technology for both functional genetics studies and potential control of O. cumana. The ease and effectiveness of this strategy could potentially be useful for other species provided they are amenable to SSA.
大花草是一种全寄生植物,它附着在宿主植物的根部,严重降低了向日葵(Helianthus annuus L.)的产量。目前仅发现少数遗传抗性来源,缺乏有效的控制方法。本研究建立了种子浸泡接种(SSA)方法,并构建了重组烟草脆裂病毒载体,以表达 RNA 干扰(RNAi)诱导物,在向日葵中引起病毒诱导的基因沉默(VIGS)。通过 SSA-VIGS 方法,宿主靶基因 HaTubulin 在叶片和根组织中均被系统性沉默。通过 11 个靶基因中的 10 个证实了跨物种的大花草基因沉默,沉默效率为 23.43%-92.67%。靶标 OcQR1、OcCKX5 和 OcWRI1 基因的敲低减少了吸器的数量,而 OcEXPA6 基因的沉默导致了更严重的表型异常,如短结节和坏死。OcEXPA6 基因的过表达导致苜蓿(Medicago sativa)根生长迟缓。结果表明,这些基因在大花草寄生过程中发挥着重要作用。高通量小 RNA(sRNA)测序和生物信息学分析揭示了大花草中靶基因衍生 siRNA 的独特特征,如 siRNA 转导性、链极性、热点区域和 21/22-nt siRNA 优势,后者通过 Northern blot 实验得到了证实。通过分析大花草中的 RNAi 机制基因,也讨论了可能的 RNAi 机制。总之,我们为大花草的功能遗传学研究和潜在控制建立了一种高效的宿主诱导基因沉默技术。只要宿主植物可接受 SSA,这种策略的简便性和有效性可能对其他物种也有用。