Kuprina Kristina, Haldan Kerstin, Saenko Stepan, Gulam Mohamed Safwaan, Kreyling Jürgen, Schnittler Martin, Bog Manuela
Institute of Botany and Landscape Ecology, University of Greifswald, Soldmannstraße 15, 17489, Greifswald, Germany.
Institute of Mathematics and Computer Science, University of Greifswald, Walther-Rathenau-Straße 47, 17489, Greifswald, Germany.
Plant Cell Rep. 2025 Aug 12;44(9):197. doi: 10.1007/s00299-025-03585-9.
Key drought-response genes regulate saccharopine, mevalonate, water-stress pathways, and cell wall remodeling. Ploidy level influences gene expression under drought and non-stress conditions. Octoploids overall exhibit lower methylation than tetraploids. Drought stress significantly affects plant physiology and growth, yet the molecular mechanisms underlying drought responses remain poorly understood. In this study, we investigate how tetraploid and octoploid Phragmites australis (common reed), a key species in wetland ecosystems and paludiculture, respond to drought at the transcriptional and epigenetic levels. Using RNA-seq, we identify changes in gene expression after 20 and 30 days of drought and assess methylation-sensitive amplification polymorphism (MSAP) over 50 days of drought. Transcriptomic analysis reveals that key drought-response genes are shared between ploidy levels, including those involved in the saccharopine pathway, water deprivation response, cell wall remodeling, and the mevalonate pathway. Drought suppresses photosynthetic genes, with PsbP downregulated by up to 32-fold. Ploidy level influences gene expression under both drought and non-stress conditions, highlighting distinct adaptive strategies. In control samples, gene expression differed between ploidy levels, with octoploids upregulating genes related to translation and metabolism, while tetraploids activate genes involved in cell wall modification and transmembrane transport. Prolonged drought increases DNA methylation variability, though no significant correlation was detected between methylation levels and drought duration. Methylation differences are more pronounced between ploidy levels, with octoploids exhibiting lower overall methylation. These findings highlight the complex interactions between gene expression, epigenetic modifications, and polyploidy in drought response and provide a theoretical framework for future selection, hybridization, and conservation initiatives.
关键的干旱响应基因调控酵母氨酸、甲羟戊酸、水分胁迫途径以及细胞壁重塑。倍性水平在干旱和非胁迫条件下影响基因表达。八倍体总体上比四倍体表现出更低的甲基化水平。干旱胁迫显著影响植物生理和生长,然而干旱响应背后的分子机制仍知之甚少。在本研究中,我们调查四倍体和八倍体芦苇(一种湿地生态系统和沼泽地栽培中的关键物种)在转录和表观遗传水平上如何响应干旱。使用RNA测序,我们确定干旱20天和30天后基因表达的变化,并评估50天干旱期间的甲基化敏感扩增多态性(MSAP)。转录组分析表明,关键的干旱响应基因在不同倍性水平之间是共享的,包括那些参与酵母氨酸途径、缺水响应、细胞壁重塑和甲羟戊酸途径的基因。干旱抑制光合基因,其中光系统II外周蛋白(PsbP)下调高达32倍。倍性水平在干旱和非胁迫条件下均影响基因表达,突出了不同的适应策略。在对照样本中,不同倍性水平之间的基因表达存在差异,八倍体上调与翻译和代谢相关的基因,而四倍体激活参与细胞壁修饰和跨膜运输的基因。长期干旱增加了DNA甲基化变异性,尽管未检测到甲基化水平与干旱持续时间之间的显著相关性。倍性水平之间的甲基化差异更为明显,八倍体总体甲基化水平较低。这些发现突出了干旱响应中基因表达、表观遗传修饰和多倍性之间的复杂相互作用,并为未来的选择、杂交和保护计划提供了理论框架。