Pandey Shree P, Chen Chen, Singh Shivam, Maniar Jalak N, Mishra Avinash, Bakshi Suman, Mishra V K, Sharma Sandeep
College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou, China.
Jiangsu Key Laboratory of Crop Genetics and Physiology, Co-Innovation Center for Modern Production Technology of Grain Crops, Key Laboratory of Plant Functional Genomics of the Ministry of Education, Yangzhou University, Yangzhou, China.
Plant Cell Rep. 2025 May 21;44(6):124. doi: 10.1007/s00299-025-03515-9.
Our study unravels a complex multi-layered molecular response of peanut roots to salinity, where reprograming of gene-expression is partly executed by changes in methylome via RdDM pathway and exerted through transcription factors. Peanut (Arachis hypogaea L.) is a major oilseed crop of global importance, whose production is severely impacted by salinity. Here, we have explored the transcriptional response of peanut roots to salinity stress using deep sequencing. Further, we have unravelled the salinity-induced changes in peanut root methylome. When peanut seedlings were grown under high-salt conditions for 7 days, their root and shoot growth was significantly impaired. A large-scale transcriptional reprogramming was recorded where 1926 genes were down- and 3260 genes were up-regulated due to salt stress in peanut roots. The molecular response of peanut root comprised several layers of regulators, which included the genes related to ion transport, osmolyte accumulation, signal transduction, and salt stress-responsive genes. Several negative regulators are also differentially expressed in peanut roots, which may contribute to its susceptibility. This response is regulated by a large number of transcription factors (TFs) and epigenetically by changes in DNA methylation. The DNA methylation changes in roots were highly complex and context dependent when exposed to salt stress. An inverse relationship between the changes in gene expression and methylation status was partially observed for several important gene sets and TFs. A treatment with 5'-azacytidine recovered the inhibitory impact of salt stress in peanut roots. Thus, a complex multilayered molecular response to salinity in peanut roots was observed. A part of this response may be modulated by the reprogramming of RNA-directed DNA methylation pathway. This investigation also serves as a resource for future gene-mining and methylation studies for improving peanut resistance to salt stress.
我们的研究揭示了花生根系对盐胁迫的复杂多层分子反应,其中基因表达的重编程部分是通过RNA介导的DNA甲基化(RdDM)途径引起的甲基化组变化来执行的,并通过转录因子发挥作用。花生(Arachis hypogaea L.)是一种具有全球重要性的主要油料作物,其产量受到盐胁迫的严重影响。在这里,我们利用深度测序技术探索了花生根系对盐胁迫的转录反应。此外,我们还揭示了盐胁迫诱导的花生根甲基化组变化。当花生幼苗在高盐条件下生长7天时,其根和地上部分的生长受到显著抑制。记录到大规模的转录重编程,由于盐胁迫,花生根中有1926个基因下调,3260个基因上调。花生根的分子反应包括几层调节因子,其中包括与离子转运、渗透溶质积累、信号转导以及盐胁迫响应基因相关的基因。一些负调节因子在花生根中也有差异表达,这可能导致其易感性。这种反应受到大量转录因子(TFs)的调节,并且在表观遗传上受到DNA甲基化变化的影响。当暴露于盐胁迫时,根中的DNA甲基化变化高度复杂且依赖于上下文。对于几个重要的基因集和转录因子,部分观察到基因表达变化与甲基化状态之间的负相关关系。用5'-氮杂胞苷处理可恢复盐胁迫对花生根的抑制作用。因此,观察到花生根对盐胁迫的复杂多层分子反应。这种反应的一部分可能通过RNA指导的DNA甲基化途径的重编程来调节。这项研究还为未来改善花生抗盐胁迫的基因挖掘和甲基化研究提供了资源。