Long Ping Branch, Graduate School of Hunan University, Changsha 410125, China.
Key Laboratory of Plant Resource Conservation and Sustainable Utilization, Key Laboratory of Post-Harvest Handling of Fruits, Ministry of Agriculture, Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China.
Cells. 2020 Feb 4;9(2):363. doi: 10.3390/cells9020363.
The Dicer protein is one of the most important components of RNAi machinery because it regulates the production of small RNAs (sRNAs) in eukaryotes. Here, Dicer1-like gene (Pit-DCL1) and Dicer2-like gene (Pit-DCL2) RNAi transformants were generated via pSilent-1 in (Pit), which is the causal agent of citrus blue mold. Neither transformant showed a change in mycelial growth or sporulation ability, but the pathogenicity of the Pit-DCL2 RNAi transformant to citrus fruits was severely impaired, compared to that of the Pit-DCL1 RNAi transformant and the wild type. We further developed a citrus wound-mediated RNAi approach with a double-stranded fragment of Pit-DCL2 generated in vitro, which achieved an efficiency in reducing expression and virulence that was similar to that of protoplast-mediated RNAi in suggesting that this approach is promising in the exogenous application of dsRNA to control pathogens on the surface of citrus fruits. In addition, sRNA sequencing revealed a total of 69.88 million potential sRNAs and 12 novel microRNA-like small RNAs (milRNAs), four of which have been predicated on target innate immunity or biotic stress-related genes in Valencia orange. These data suggest that both the Pit-DCL1 and Pit-DCL2 RNAi transformants severely disrupted the biogenesis of the potential milRNAs, which was further confirmed for some milRNAs by qRT-PCR or Northern blot analysis. These data suggest the sRNAs in that may be involved in a molecular virulence mechanism termed cross-kingdom RNAi (ck-RNAi) by trafficking sRNA from to citrus fruits.
Dicer 蛋白是 RNAi 机制中最重要的成分之一,因为它调节真核生物中小 RNA(sRNA)的产生。在这里,通过 pSilent-1 在 (Pit)中生成了 Dicer1 样基因(Pit-DCL1)和 Dicer2 样基因(Pit-DCL2)RNAi 转化体,Pit 是柑橘青霉病的病原体。两种转化体的菌丝生长或产孢能力都没有变化,但与 Pit-DCL1 RNAi 转化体和野生型相比,Pit-DCL2 RNAi 转化体对柑橘果实的致病性严重受损。我们进一步开发了一种柑橘伤口介导的 RNAi 方法,用体外产生的 Pit-DCL2 的双链片段,实现了降低 表达和毒力的效率,与原生质体介导的 RNAi 相似,表明该方法在外源应用 dsRNA 控制柑橘果实表面病原体方面很有前景。此外,sRNA 测序共揭示了 6988 万个潜在的 sRNA 和 12 个新的 microRNA 样小 RNA(milRNA),其中 4 个已经预测到瓦伦西亚橙中先天免疫或生物胁迫相关基因的靶基因。这些数据表明,Pit-DCL1 和 Pit-DCL2 RNAi 转化体严重破坏了潜在 milRNA 的生物发生,通过 qRT-PCR 或 Northern blot 分析进一步证实了一些 milRNA。这些数据表明,柑橘青霉病中的 sRNA 可能通过将 sRNA 从 转移到柑橘果实来参与一种称为跨物种 RNAi(ck-RNAi)的分子毒力机制。