Provincial Key Laboratory of Agrobiology, Institute of Crop Germplasm and Biotechnology, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, Jiangsu, China.
Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, Jiangsu, China.
BMC Plant Biol. 2018 Jun 4;18(1):104. doi: 10.1186/s12870-018-1332-3.
Long Noncoding-RNAs (LncRNAs) are known to be involved in some biological processes, but their roles in plant-virus interactions remain largely unexplored. While circular RNAs (circRNAs) have been studied in animals, there has yet to be extensive research on them in a plant system, especially in tomato-tomato yellow leaf curl virus (TYLCV) interaction.
In this study, RNA transcripts from the susceptible tomato line JS-CT-9210 either infected with TYLCV or untreated, were sequenced in a pair-end strand-specific manner using ribo-zero rRNA removal library method. A total of 2056 lncRNAs including 1767 long intergenic non-coding RNA (lincRNAs) and 289 long non-coding natural antisense transcripts (lncNATs) were obtained. The expression patterns in lncRNAs were similar in susceptible tomato plants between control check (CK) and TYLCV infected samples. Our analysis suggested that lncRNAs likely played a role in a variety of functions, including plant hormone signaling, protein processing in the endoplasmic reticulum, RNA transport, ribosome function, photosynthesis, glulathione metabolism, and plant-pathogen interactions. Using virus-induced gene silencing (VIGS) analysis, we found that reduced expression of the lncRNA S-slylnc0957 resulted in enhanced resistance to TYLCV in susceptible tomato plants. Moreover, we identified 184 circRNAs candidates using the CircRNA Identifier (CIRI) software, of which 32 circRNAs were specifically expressed in untreated samples and 83 circRNAs in TYLCV samples. Approximately 62% of these circRNAs were derived from exons. We validated the circRNAs by both PCR and Sanger sequencing using divergent primers, and found that most of circRNAs were derived from the exons of protein coding genes. The silencing of these circRNAs parent genes resulted in decreased TYLCV virus accumulation.
In this study, we identified novel lncRNAs and circRNAs using bioinformatic approaches and showed that these RNAs function as negative regulators of TYLCV infection. Moreover, the expression patterns of lncRNAs in susceptible tomato plants were different from that of resistant tomato plants, while exonic circRNAs expression positively associated with their respective protein coding genes. This work provides a foundation for elaborating the novel roles of lncRNAs and circRNAs in susceptible tomatoes following TYLCV infection.
长链非编码 RNA(lncRNAs)已知参与一些生物过程,但它们在植物-病毒相互作用中的作用在很大程度上仍未得到探索。虽然环状 RNA(circRNAs)在动物中已有研究,但在植物系统中对它们的研究还很有限,特别是在番茄-番茄黄曲叶病毒(TYLCV)相互作用中。
在这项研究中,使用核糖体零 rRNA 去除文库方法,以对端测序的方式,对易感性番茄系 JS-CT-9210 进行 TYLCV 感染或未处理的 RNA 转录物进行测序。总共获得了 2056 个 lncRNAs,包括 1767 个长基因间非编码 RNA(lincRNAs)和 289 个长非编码自然反义转录本(lncNATs)。在对照检查(CK)和 TYLCV 感染样品之间,易感性番茄植物中的 lncRNAs 表达模式相似。我们的分析表明,lncRNAs 可能在多种功能中发挥作用,包括植物激素信号转导、内质网中蛋白质加工、RNA 转运、核糖体功能、光合作用、谷胱甘肽代谢和植物-病原体相互作用。使用病毒诱导基因沉默(VIGS)分析,我们发现易感性番茄植物中 lncRNA S-slylnc0957 的表达降低导致对 TYLCV 的抗性增强。此外,我们使用 CircRNA Identifier(CIRI)软件鉴定了 184 个候选 circRNAs,其中 32 个 circRNAs 仅在未处理的样品中特异性表达,83 个 circRNAs 在 TYLCV 样品中表达。这些 circRNAs 中约 62%来源于外显子。我们使用差异引物通过 PCR 和 Sanger 测序验证了这些 circRNAs,并发现大多数 circRNAs 来源于蛋白质编码基因的外显子。这些 circRNAs 亲本基因的沉默导致 TYLCV 病毒积累减少。
在这项研究中,我们使用生物信息学方法鉴定了新的 lncRNAs 和 circRNAs,并表明这些 RNA 作为 TYLCV 感染的负调控因子发挥作用。此外,易感性番茄植物中 lncRNAs 的表达模式与抗性番茄植物的表达模式不同,而外显子 circRNAs 的表达与相应的蛋白质编码基因呈正相关。这项工作为阐述 TYLCV 感染后易感番茄中 lncRNAs 和 circRNAs 的新作用提供了基础。