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Transcriptome Profiling and Characterization of Drought-Tolerant Potato Plant (Solanum tuberosum L.)

机译:耐旱马铃薯植株的转录组谱分析与特征分析

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摘要

Potato (Solanum tuberosum L.) is the third most important food crop, and breeding drought-tolerant varieties is vital research goal. However, detailed molecular mechanisms in response to drought stress in potatoes are not well known. In this study, we developed EMS-mutagenized potatoes that showed significant tolerance to drought stress compared to the wild-type (WT) ‘Desiree’ cultivar. In addition, changes to transcripts as a result of drought stress in WT and drought-tolerant (DR) plants were investigated by de novo assembly using the Illumina platform. One-week-old WT and DR plants were treated with −1.8 Mpa polyethylene glycol-8000, and total RNA was prepared from plants harvested at 0, 6, 12, 24, and 48 h for subsequent RNA sequencing. In total, 61,100 transcripts and 5,118 differentially expressed genes (DEGs) displaying up- or down-regulation were identified in pairwise comparisons of WT and DR plants following drought conditions. Transcriptome profiling showed the number of DEGs with up-regulation and down-regulation at 909, 977, 1181, 1225 and 826 between WT and DR plants at 0, 6, 12, 24, and 48 h, respectively. Results of KEGG enrichment showed that the drought tolerance mechanism of the DR plant can mainly be explained by two aspects, the ‘photosynthetic-antenna protein’ and ‘protein processing of the endoplasmic reticulum’. We also divided eight expression patterns in four pairwise comparisons of DR plants (DR0 vs DR6, DR12, DR24, DR48) under PEG treatment. Our comprehensive transcriptome data will further enhance our understanding of the mechanisms regulating drought tolerance in tetraploid potato cultivars.
机译:马铃薯(Solanum tuberosum L.)是第三重要的粮食作物,育种耐旱品种是至关重要的研究目标。但是,响应马铃薯干旱胁迫的详细分子机制尚不清楚。在这项研究中,我们开发了EMS诱变马铃薯,与野生型(Desiree)品种相比,它们对干旱胁迫表现出显着的耐受性。此外,通过使用Illumina平台从头组装研究了野生型和耐旱(DR)植物中干旱胁迫导致的转录本变化。用-1.8 Mpa聚乙二醇-8000处理一星期大的WT和DR植物,并从0、6、12、24和48 h收获的植物中制备总RNA,用于随后的RNA测序。在干旱条件下WT和DR植物的成对比较中,总共鉴定出61,100个转录本和5,118个差异表达基因(DEG),它们表达上调或下调。转录组分析显示,在0、6、12、24和48 h时,WT和DR植物在909、977、1181、1225和826处上调和下调的DEG数量。 KEGG富集的结果表明,DR植物的抗旱机理主要可以从“光合天线蛋白”和“内质网蛋白加工”两个方面来解释。我们还在PEG处理下的DR植物(DR0与DR6,DR12,DR24,DR48)的四个成对比较中划分了八个表达模式。我们全面的转录组数据将进一步增进我们对调节四倍体马铃薯品种耐旱性机制的了解。

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