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Identification of drought-responsive and novel Populus trichocarpa microRNAs by high-throughput sequencing and their targets using degradome analysis

机译:高通量测序鉴定抗干旱和新型毛果杨microRNA及其降解组的目标

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Background MicroRNAs (miRNAs) are endogenous small RNAs (sRNAs) with a wide range of regulatory functions in plant development and stress responses. Although miRNAs associated with plant drought stress tolerance have been studied, the use of high-throughput sequencing can provide a much deeper understanding of miRNAs. Drought is a common stress that limits the growth of plants. To obtain more insight into the role of miRNAs in drought stress, Illumina sequencing of Populus trichocarpa sRNAs was implemented. Results Two sRNA libraries were constructed by sequencing data of control and drought stress treatments of poplar leaves. In total, 207 P. trichocarpa conserved miRNAs were detected from the two sRNA libraries. In addition, 274 potential candidate miRNAs were found; among them, 65 candidates with star sequences were chosen as novel miRNAs. The expression of nine conserved miRNA and three novel miRNAs showed notable changes in response to drought stress. This was also confirmed by quantitative real time polymerase chain reaction experiments. To confirm the targets of miRNAs experimentally, two degradome libraries from the two treatments were constructed. According to degradome sequencing results, 53 and 19 genes were identified as targets of conserved and new miRNAs, respectively. Functional analysis of these miRNA targets indicated that they are involved in important activities such as the regulation of transcription factors, the stress response, and lipid metabolism. Conclusions We discovered five upregulated miRNAs and seven downregulated miRNAs in response to drought stress. A total of 72 related target genes were detected by degradome sequencing. These findings reveal important information about the regulation mechanism of miRNAs in P. trichocarpa and promote the understanding of miRNA functions during the drought response.
机译:背景技术MicroRNA(miRNA)是内源性小RNA(sRNA),在植物发育和胁迫响应中具有广泛的调控功能。尽管已经研究了与植物干旱胁迫耐受性相关的miRNA,但高通量测序的使用可以提供对miRNA的更深入的了解。干旱是限制植物生长的常见压力。为了更深入地了解miRNA在干旱胁迫中的作用,实施了毛果杨sRNA的Illumina测序。结果通过对杨树叶片对照和干旱胁迫处理的数据进行测序,构建了两个sRNA文库。总共从两个sRNA文库中检测到207个毛果杨假单胞菌保守的miRNA。此外,发现了274个潜在的候选miRNA;其中,选择65个具有星形序列的候选基因作为新型miRNA。九个保守的miRNA和三个新的miRNA的表达显示出对干旱胁迫的显着变化。定量实时聚合酶链反应实验也证实了这一点。为了通过实验确定miRNA的靶标,构建了两种处理方法的两个降解组文库。根据降解组测序结果,分别鉴定出53个和19个基因为保守和新miRNA的靶标。这些miRNA靶标的功能分析表明,它们参与了重要的活动,例如转录因子的调节,应激反应和脂质代谢。结论我们发现了5个上调的miRNA和7个下调的miRNA响应干旱胁迫。降解组测序共检测到72个相关靶基因。这些发现揭示了关于毛果杨中miRNA调控机制的重要信息,并促进了干旱反应期间对miRNA功能的了解。

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