The effect of drought stress on enzymatic and molecular changes of some antioxidants in parental and mutant bread wheat genotype using RNAseq. data
| Autor: | Meisam Radfar, Seyyede Sanaz Ramezanpour, Hassan Soltanloo, Leila Kianmehr |
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| Jazyk: | perština |
| Rok vydání: | 2023 |
| Předmět: | |
| Zdroj: | تنش های محیطی در علوم زراعی, Vol 16, Iss 3, Pp 765-785 (2023) |
| Druh dokumentu: | article |
| ISSN: | 2228-7604 2383-3084 |
| DOI: | 10.22077/escs.2023.4970.2094 |
| Popis: | IntroductionWheat (Triticum aestivum L.) is one of the most important grains used in the world and its production is reduced in different regions due to drought stress. the plant antioxidant system can scavenge the reactive oxygen species (ROS) produced under drought. Induction of mutation using gamma ray is one of the common methods for genetic modification and identification of tolerant and resistant mutants. Mutant T65-58-8 is one of these drought tolerant genotypes that has been obtained by irradiation to Tabasi wheat genotype. The wheat plant needs irrigation during the flowering stage and drought stress is very important in this stage. In this study, in the flowering stage, the enzymes superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) and glutathione peroxidase (GPX) involved in the mechanisms of tolerance to oxidative damage of ROS in the flag leaf were studied and the expression of the genes related to these enzymes was investigated using RNAseq. method.Materials and methodsDrought stress was applied based on field capacity (FC). The experiment was performed as a factorial experiment in a completely randomized design with three replications. Factors studied in this experiment include genotype at two levels (Tabasi parent and Mutant T65-58-8) and drought stress at 5 levels (100% FC or control, 75%, 22%, re-sampling from control pots at 18% FC and sampling after re-irrigation to the pot when had 90% FC). Wheat growth stages can be studied by Zadoks index. SOD activity was measured by Minami and Yoshikawa method, CAT activity by Aebi method, GR activity by Foyer and Halliwell method and GPX activity by Hopkins and Tudhope method. RNA sequencing was performed using Illumina NovaSeq 6000. Gene expression was obtained based on sequencing data by Bowtie2, Tophat2, HTseq-count and Featurecount softwares. After normalization by generating FPKM, Log2FC gene expression was calculated.Results and discussionExamination of superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) and glutathione peroxidase (GPX) indices showed a significant difference (p |
| Databáze: | Directory of Open Access Journals |
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