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Prediction of novel miRNAs and associated target genes in Glycine max

机译:甘氨酸中新型miRNA和相关靶基因的预测

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Background: Small non-coding RNAs (21 to 24 nucleotides) regulate a number of developmental processes in plants and animals by silencing genes using multiple mechanisms. Among these, the most conserved classes are microRNAs (miRNAs) and small interfering RNAs (siRNAs), both of which are produced by RNase Ill-like enzymes called Dicers. Many plant miRNAs play critical roles in nutrient homeostasis, developmental processes, abiotic stress and pathogen responses. Currently, only 70 miRNA have been identified in soybean.Methods: We utilized lllumina's SBS sequencing technology to generate high-quality small RNA (sRNA) data from four soybean (Glycine max) tissues, including root, seed, flower, and nodules, to expand the collection of currently known soybean miRNAs. We developed a bioinformatics pipeline using in-house scripts and publicly available structure prediction tools to differentiate the authentic mature miRNA sequences from other sRNAs and short RNA fragments represented in the public sequencing data. Results: The combined sequencing and bioinformatics analyses identified 129 miRNAs based on hairpin secondary structure features in the predicted precursors. Out of these, 42 miRNAs matched known miRNAs in soybean or other species, while 87 novelmiRNAs were identified. We also predicted the putative target genes of all identified miRNAs with computational methods and verified the predicted cleavage sites in vivo for a subset of these targets using the 5' RACE method. Finally, we also studied the relationship between the abundance of miRNA and that of the respective target genes by comparison to Solexa cDNA sequencing data. Conclusion: Our study significantly increased the number of miRNAs known to be expressed in soybean. The bioinformatics analysis provided insight on regulation patterns between the miRNAs and their predicted target genes expression. We also deposited the data in a soybean genome browser based on the UCSC Genome Browser architecture. Using the browser, we annotated the soybean data with miRNA sequences from four tissues and cDNA sequencing data. Overlaying these two datasets in the browser allows researchers to analyze the miRNA expression levels relative to that of the associated target genes. The browser can be accessed at http://digbio. missouri.edu/soybean mirna/.
机译:背景:小非编码RNA(21至24核苷酸)通过使用多种机制来调节植物和动物中的许多发育过程。其中,最保守的类是MicroRNA(miRNA)和小干扰RNA(siRNA),两者都是由称为Dicers的RNase不含酶产生的。许多植物miRNA在营养稳态,发育过程,非生物应激和病原体反应中起重要作用。目前,在大豆中仅识别出70 miRNA。方法:我们利用Lllumina的SBS测序技术,从四种大豆(甘氨酸最大)组织中产生高质量的小RNA(SRNA)数据,包括根,种子,花和结节,包括扩展当前已知的大豆MiRNA的集合。我们使用内部脚本和公开的结构预测工具开发了一种生物信息学管道,并公开可用的结构预测工具从公共测序数据中所示的其他SRNA和短RNA片段区分原始成熟miRNA序列。结果:组合测序和生物信息学分析基于预测前体的发夹二级结构特征鉴定了129 miRNA。在这些中,42名MiRNA匹配大豆或其他物种中的已知miRNA,而鉴定了87种新闻。我们还预测了所有鉴定的miRNA的推定靶基因,并使用该5'播种方法验证了这些靶标的预测的裂解位点。最后,我们还通过与SOLEXA cDNA测序数据相比,研究了MiRNA丰富与各个靶基因的关系之间的关系。结论:我们的研究显着提高了在大豆中表达的miRNA的数量。生物信息学分析提供了对miRNA和预测靶基因表达之间的调控模式的洞察。我们还基于UCSC基因组浏览器架构存放了大豆基因组浏览器中的数据。使用浏览器,我们用来自四种组织和cDNA测序数据的miRNA序列注释了大豆数据。覆盖浏览器中的这两个数据集允许研究人员相对于相关靶基因的研究分析miRNA表达水平。浏览器可以访问http:// digbio。 missouri.edu/soybean mirna /。

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