Department of Biology, Faculty of Science and Arts, Marmara University, Istanbul, Turkey.
Department of Biology, Faculty of Science, Kyrgyz-Turkish Manas University, Bishkek, Kyrgyzstan.
Mol Biol Rep. 2019 Jun;46(3):2703-2711. doi: 10.1007/s11033-019-04714-w. Epub 2019 Mar 25.
Aluminum (Al) is one of the most important stress factors that reduce plant productivity in acidic soils. Present work thereby analyzed Al-induced genomic alterations in Bryophyllum daigremontianum clones using RAPD and ISSR markers, and investigated responding changes in photosynthetic pigment (chlorophyll a, b, a/b, total chlorophyll and carotenoid) contents and total soluble protein amounts in plant leaves. The main reason for the use of bulbiferous spurs originated clone plants was to increase reliability and acceptability of RAPD and ISSR techniques in DNA fingerprinting. Raised 40 clone plants were divided into five separate groups each with eight individuals and each experimental group was watered with 0 (control), 0 (acid control), 50, 100 and 200 µM AlCl-containing Hoagland solutions on alternate days for two and a half months. All plant soils except control group were sprayed with 0.2% sulfuric acid following watering days and this contributed acidic characteristic (pH 4.8) to soil structure. Increase in Al concentrations were accompanied by an increase in total soluble protein amounts, a decrease in photosynthetic pigment contents, and with appearance, disappearance and intensity changes at RAPD and ISSR band profiles. Out of tested RAPD1-25 and ISSR1-15 primers, RAPD8, RAPD9, ISSR2 and ISSR7 primers produced reproducible band profiles that were distinguishable between treatment and control groups. Findings showed that RAPD and ISSR fingerprints have been useful biomarkers for investigation of plant genotoxicity, especially in clone plants. Moreover, if these fingerprints are integrated with other physiological parameters they could become more powerful tools in ecotoxicology.
铝(Al)是降低酸性土壤中植物生产力的最重要应激因素之一。本工作因此使用 RAPD 和 ISSR 标记分析了落地生根克隆体中 Al 诱导的基因组改变,并研究了植物叶片中光合色素(叶绿素 a、b、a/b、总叶绿素和类胡萝卜素)含量和总可溶性蛋白含量的响应变化。使用具有鳞茎状刺突起源的克隆植物的主要原因是提高 RAPD 和 ISSR 技术在 DNA 指纹分析中的可靠性和可接受性。培养了 40 株克隆植物,将它们分为五组,每组 8 株,每个实验组每隔一天用含有 0(对照)、0(酸对照)、50、100 和 200 μM AlCl 的 Hoagland 溶液浇水,共持续两个半月。除对照组外,所有植物土壤在浇水后都用 0.2%硫酸喷洒,这使土壤结构具有酸性特征(pH 4.8)。随着 Al 浓度的增加,总可溶性蛋白含量增加,光合色素含量降低,RAPD 和 ISSR 带谱出现、消失和强度变化。在所测试的 RAPD1-25 和 ISSR1-15 引物中,RAPD8、RAPD9、ISSR2 和 ISSR7 引物产生了可在处理组和对照组之间区分的可重复的带谱。研究结果表明,RAPD 和 ISSR 指纹图谱已成为研究植物遗传毒性的有用生物标志物,特别是在克隆植物中。此外,如果将这些指纹图谱与其他生理参数相结合,它们可能成为生态毒理学中更强大的工具。