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首页> 外文期刊>Plant Cell Reports >Transcriptome dynamics of a desert poplar (Populus pruinosa) in response to continuous salinity stress
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Transcriptome dynamics of a desert poplar (Populus pruinosa) in response to continuous salinity stress

机译:沙漠杨(Populus pruinosa)响应连续盐分胁迫的转录组动力学

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摘要

Using RNA sequencing analysis, we identified 9,216 regulatory and salt-related genes with differential expression and temporal expression trends which provide a clear picture of transcriptomic dynamics in response to continuous salinity stress in a desert poplar, Populus pruinosa. Populus pruinosa Schrenk is native to the desert region of western China and extraordinarily well adapted to the local salt stress. Thus, it is an ideal model for studying plants' adaptation to salt stress, but its transcriptomic responses have not been previously characterized. Thus, we analyzed time- courses of these responses via a series of sequencings. In total, we generated 157.4 million 100 bp paired-end clean reads and identified 9,216 differentially expressed genes (DEGs) between salt-stressed calli and controls. Gene ontology classification analysis revealed that salt stress-related categories--including 'oxidation reduction', 'transcription factor activity', 'membrane' and 'ion channel activity'aEuro"aEuro"were highly enriched among these DEGs. In addition, we grouped the 9,216 DEGs by their expression dynamics into four clusters, and the genes in each cluster showed enrichment for particular functional categories. We also found that most DEGs were activated within 24 h of the stress and their expression stabilized after 48 h. All these findings suggest that gene expression rapidly and coordinately changes during this species' adaptation to salt stress. In addition, the identified DEGs provide critical genetic resources for further functional analyses and indications of potential transgenic modifications for developing salt-tolerant poplars.
机译:使用RNA测序分析,我们确定了9,216个具有差异表达和时间表达趋势的调控基因和盐相关基因,这些基因提供了转录组动力学的清晰画面,以响应沙漠化杨树Populus pruinosa的持续盐分胁迫。胡杨(Populus pruinosa Schrenk)原产于中国西部的沙漠地区,非常适合当地的盐胁迫。因此,它是研究植物对盐胁迫适应性的理想模型,但是其转录组反应先前尚未被表征。因此,我们通过一系列测序分析了这些响应的时程。总共,我们产生了1.574亿个100 bp的配对末端清洁读段,并鉴定了盐胁迫的愈伤组织和对照之间的9,216个差异表达基因(DEG)。基因本体分类分析表明,与盐胁迫相关的类别-包括“氧化还原”,“转录因子活性”,“膜”和“离子通道活性” aEuro“ aEuro”在这些DEG中高度丰富。此外,我们将9,216个DEGs的表达动态分为四个簇,每个簇中的基因均显示出特定功能类别的丰富性。我们还发现,大多数DEGs在应激后24小时内被激活,其表达在48小时后稳定下来。所有这些发现表明,在该物种对盐胁迫的适应过程中,基因表达迅速而协调地变化。此外,已鉴定的DEG为进一步的功能分析和开发耐盐杨树的潜在转基因修饰提供了重要的遗传资源。

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