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Comprehensive Transcriptome Profiling and Identification of Potential Genes Responsible for Salt Tolerance in Tall Fescue Leaves under Salinity Stress

机译:盐胁迫下高羊茅叶片综合转录组分析和潜在耐盐基因的鉴定

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摘要

Soil salinity is a serious threat to plant growth and crop productivity. Tall fescue utilization in saline areas is limited by its inferior salt tolerance. Thus, a transcriptome study is a prerequisite for future research aimed at providing deeper insights into the molecular mechanisms of tall fescue salt tolerance as well as molecular breeding. Recent advances in sequencing technology offer a platform to achieve this. Here, Illumina RNA sequencing of tall fescue leaves generated a total of 144,339 raw reads. After de novo assembly, unigenes with a total length of 129,749,938 base pairs were obtained. For functional annotations, the unigenes were aligned to various databases. Further structural analyses revealed 79,352 coding DNA sequences and 13,003 microsatellites distributed across 11,277 unigenes as well as single nucleotide polymorphisms. In total, 1862 unigenes were predicted to encode for 2120 transcription factors among which most were key salt-responsive. We determined differential gene expression and distribution per sample and most genes related to salt tolerance and photosynthesis were upregulated in 48 h vs. 24 h salt treatment. Protein interaction analysis revealed a high interaction of chaperonins and Rubisco proteins in 48 h vs. 24 h salt treatment. The gene expressions were finally validated using quantitative polymerase chain reaction (qPCR), which was coherent with sequencing results.
机译:土壤盐分严重威胁植物的生长和作物的生产力。在盐碱地区高羊茅利用度受到其耐盐性差的限制。因此,转录组研究是未来研究的先决条件,其目的是提供对高羊茅耐盐性的分子机制以及分子育种的更深入了解。测序技术的最新进展为实现这一目标提供了平台。在这里,高羊茅叶片的Illumina RNA测序产生了144,339个原始读段。从头组装后,获得了总长度为129,749,938个碱基对的单基因。对于功能注释,将单基因与各种数据库对齐。进一步的结构分析显示,分布在11,277个单基因中的79,352个编码DNA序列和13,003个微卫星以及单核苷酸多态性。总的来说,预计有1862个单基因编码2120个转录因子,其中大多数是关键的盐反应性。我们确定了每个样品的差异基因表达和分布,并且与盐耐受性和光合作用相关的大多数基因在48小时和24小时盐处理中均被上调。蛋白质相互作用分析显示,伴侣盐和Rubisco蛋白在48小时和24小时盐处理中具有高度相互作用。最后使用定量聚合酶链反应(qPCR)验证了基因表达,这与测序结果一致。

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