首页> 外文期刊>Forests >Genome-Wide Analysis of Gene and microRNA Expression in Diploid and Autotetraploid Paulownia fortunei (Seem) Hemsl. under Drought Stress by Transcriptome, microRNA, and Degradome Sequencing
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Genome-Wide Analysis of Gene and microRNA Expression in Diploid and Autotetraploid Paulownia fortunei (Seem) Hemsl. under Drought Stress by Transcriptome, microRNA, and Degradome Sequencing

机译:在二倍体和同源四倍体桐木(Seem)Hemsl中进行基因和microRNA表达的全基因组分析。转录组,microRNA和降解组测序在干旱胁迫下

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Drought is a common and recurring climatic condition in many parts of the world, and it can have disastrous impacts on plant growth and development. Many genes involved in the drought response of plants have been identified. Transcriptome, microRNA (miRNA), and degradome analyses are rapid ways of identifying drought-responsive genes. The reference genome sequence of Paulownia fortunei (Seem) Hemsl. is now available, which makes it easier to explore gene expression, transcriptional regulation, and post-transcriptional in this species. In this study, four transcriptome, small RNA, and degradome libraries were sequenced by Illumina sequencing, respectively. A total of 258 genes and 11 miRNAs were identified for drought-responsive genes and miRNAs in P. fortunei . Degradome sequencing detected 28 miRNA target genes that were cleaved by members of nine conserved miRNA families and 12 novel miRNAs. The results here will contribute toward enriching our understanding of the response of Paulownia fortunei trees to drought stress and may provide new direction for further experimental studies related the development of molecular markers, the genetic map construction, and other genomic research projects in Paulownia.
机译:在世界许多地区,干旱是一种常见且反复出现的气候条件,对植物的生长和发育可能造成灾难性的影响。已经鉴定出许多与植物干旱反应有关的基因。转录组,microRNA(miRNA)和降解组分析是鉴定干旱响应基因的快速方法。泡桐(Seem)Hemsl的参考基因组序列。现在可以使用,这使得在该物种中探索基因表达,转录调控和转录后变得更加容易。在这项研究中,分别通过Illumina测序对四个转录组,小RNA和降解组文库进行了测序。共有258个基因和11个miRNA被鉴定为福寿螺中的干旱反应基因和miRNA。降解组测序检测到28个miRNA靶基因,这些基因被9个保守miRNA家族和12个新miRNA的成员切割。此处的结果将有助于丰富我们对泡桐树对干旱胁迫反应的理解,并可能为有关泡桐分子标记开发,遗传图谱构建和其他基因组研究项目的进一步实验研究提供新的方向。

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