Maleki Narjes, Ghorbani Abozar, Rostami Mahsa, Maina Solomon
Department of Plant Protection, Faculty of Agriculture, University of Zanjan, Zanjan, Iran.
Nuclear Agriculture Research School, Nuclear Science and Technology Research Institute (NSTRI), Karaj, Iran.
BMC Plant Biol. 2025 Apr 21;25(1):495. doi: 10.1186/s12870-025-06515-9.
Tomato plants face biotic challenges like infections by cucumber mosaic virus (CMV), a member of the Cucumovirus genus in the Bromoviridae family, as well as beneficial interactions, such as colonization by the symbiotic fungus Funneliformis mosseae, which belongs to the Glomeraceae family. While this symbiosis boosts nutrient uptake and stress tolerance, viral infections can reduce yield and quality. Understanding how tomatoes manage these interactions is vital for enhancing crop productivity. To explore the molecular mechanisms behind these interactions, this study focuses on long non-coding RNAs (lncRNAs), which play crucial roles in gene regulation, stress response, and plant metabolic pathways. Tomato RNA-seq data were analyzed to identify lncRNAs and their interactions with microRNAs (miRNAs) through de novo assembly, mapping, expression analysis, and localization prediction. In this study, 3210 lncRNAs were identified from 12 SRA datasets of tomato plants, including control, CMV-infected, F. mosseae-colonized, and co-infected samples. Among these, 3194 were novel lncRNAs and 16 were conserved. Expression analysis revealed significant differential expression patterns across treatments. Pathway analysis indicated that these lncRNAs are involved in key metabolic processes, such as carbon metabolism, amino acid biosynthesis, and secondary metabolite production, suggesting their role in enhancing disease resistance. Furthermore, we predicted interactions between identified lncRNAs and miRNAs, including miR160a, miR166a/b, miR167a, miR171a/b/c, miR1917, miR1918, and miR395a/b, thereby highlighting potential regulatory networks that could modulate stress responses. The subcellular localization of identified lncRNAs revealed a predominance in the cytoplasm, implying their involvement in post-transcriptional regulation. This study accentuates the significance of lncRNAs in tomato plant defense mechanisms and provides a foundation for future research focused on enriching resistance to viral infections and boosting stress resilience.
番茄植株面临着生物挑战,如受到黄瓜花叶病毒(CMV)的感染,CMV是雀麦花叶病毒科黄瓜病毒属的成员,同时也存在有益的相互作用,例如被属于球囊霉科的共生真菌摩西球囊霉定殖。虽然这种共生关系能促进养分吸收和胁迫耐受性,但病毒感染会降低产量和品质。了解番茄如何应对这些相互作用对于提高作物生产力至关重要。为了探究这些相互作用背后的分子机制,本研究聚焦于长链非编码RNA(lncRNA),其在基因调控、胁迫反应和植物代谢途径中发挥着关键作用。通过从头组装、映射、表达分析和定位预测,对番茄RNA测序数据进行分析,以鉴定lncRNA及其与微小RNA(miRNA)的相互作用。在本研究中,从番茄植株的12个SRA数据集中鉴定出3210个lncRNA,包括对照、CMV感染、摩西球囊霉定殖和共同感染的样本。其中,3194个是新的lncRNA,16个是保守的。表达分析揭示了不同处理之间显著的差异表达模式。通路分析表明,这些lncRNA参与关键代谢过程,如碳代谢、氨基酸生物合成和次生代谢产物生成,表明它们在增强抗病性方面的作用。此外,我们预测了鉴定出的lncRNA与miRNA之间的相互作用,包括miR160a、miR166a/b、miR167a、miR171a/b/c、miR1917、miR1918和miR395a/b,从而突出了可能调节胁迫反应的潜在调控网络。鉴定出的lncRNA的亚细胞定位显示主要位于细胞质中,这意味着它们参与转录后调控。本研究强调了lncRNA在番茄植株防御机制中的重要性,并为未来旨在增强抗病毒感染能力和提高胁迫恢复力的研究奠定了基础。