Università degli Studi di Perugia, Dept. Agricultural, Food and Environmental Sciences, Perugia, Italy.
CNR - Institute of Biosciences and Bioresources, Perugia, Italy.
Sci Rep. 2019 Jan 31;9(1):1093. doi: 10.1038/s41598-018-37496-5.
Cultivated olive, a typical fruit crop species of the semi-arid regions, could successfully face the new scenarios driven by the climate change through the selection of tolerant varieties to salt and drought stresses. In the present work, multidisciplinary approaches, including physiological, epigenetic and genetic studies, have been applied to clarify the salt tolerance mechanisms in olive. Four varieties (Koroneiki, Royal de Cazorla, Arbequina and Picual) and a related form (O. europaea subsp. cuspidata) were grown in a hydroponic system under different salt concentrations from zero to 200 mM. In order to verify the plant response under salt stress, photosynthesis, gas exchange and relative water content were measured at different time points, whereas chlorophyll and leaf concentration of Na, K and Ca ions, were quantified at 43 and 60 days after treatment, when stress symptoms became prominent. Methylation sensitive amplification polymorphism (MSAP) technique was used to assess the effects of salt stress on plant DNA methylation. Several fragments resulted differentially methylated among genotypes, treatments and time points. Real time quantitative PCR (RT-qPCR) analysis revealed significant expression changes related to plant response to salinity. Four genes (OePIP1.1, OePetD, OePI4Kg4 and OeXyla) were identified, as well as multiple retrotransposon elements usually targeted by methylation under stress conditions.
栽培橄榄是一种典型的半干旱地区水果作物,通过选择耐盐和耐旱胁迫的品种,可以成功应对气候变化带来的新情况。在本工作中,采用了包括生理、表观遗传和遗传研究在内的多学科方法,以阐明橄榄的耐盐机制。选取了四个品种(Koroneiki、Royal de Cazorla、Arbequina 和 Picual)和一个相关形式(O. europaea subsp. cuspidata),在不同盐浓度(从 0 到 200mM)的水培系统中进行种植。为了验证植物在盐胁迫下的反应,在不同时间点测量了光合作用、气体交换和相对水分含量,而在处理后 43 和 60 天时,量化了叶绿素和叶片中 Na、K 和 Ca 离子的浓度,此时胁迫症状变得明显。采用甲基化敏感扩增多态性(MSAP)技术评估盐胁迫对植物 DNA 甲基化的影响。在不同基因型、处理和时间点之间,有几个片段表现出差异甲基化。实时定量 PCR(RT-qPCR)分析显示,与植物对盐度响应相关的表达变化显著。鉴定了四个基因(OePIP1.1、OePetD、OePI4Kg4 和 OeXyla),以及在胁迫条件下通常被甲基化靶向的多个逆转座子元件。