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Genome-Wide Mapping and Analysis of Grapevine MicroRNAs and Their Potential Target Genes

机译:葡萄microRNA及其潜在靶基因的全基因组定位和分析

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MicroRNAs (miRNAs) are single-stranded, nonprotein-coding, endogenously expressed, small RNAs 19 to 25 nucleotides in length. Recognizing the lack of specific and systematic studies on genome-wide mapping of grapevine (Vitis vinifera L.) miRNAs, we conducted genome-wide mapping of Vv-miRNAs (V. vinifera miRNAs), SB-miRNAs (V. vinifera L. ‘Summer Black’ miRNAs), and Va-miRNAs (V. amurensis Rupr. miRNAs). The mapping results revealed that many of miRNAs located within the intergenic region had independent transcription units. To further validate the mapping results and existence of miRNAs, 12 randomly selected precursors of miRNAs (pre-miRNAs) were successfully cloned and sequenced. Subsequently, 15 conserved and 29 nonconserved intragenic (intronic, exonic) Vv-miRNA genes, 24 nonconserved intragenic SB-miRNA genes, and 23 nonconserved intragenic Va-miRNA genes were labeled on the basis of their locations in host genes, and 15 MIRNA clusters were detected. Interestingly, five miRNA pairs, namely, Vv-MIR395b and Vv-MIR395c, Vv-MIR482 and Vv-MIRC13, Vv-MIR172a and Va-MIR057, SB-MIR024 and Vv-MIRC35, and Vv-MIRC36 and Va-MIR073 were clustered in the host genes GSVIVT01011558001, GSVIVT01008132001, GSVIVT01031524001, GSVIVT01028156001, and GSVIVT01024516001, respectively. To validate the existence of target genes and miRNA-guided cleavage sites, 3′-end product of four predicted target messenger RNAs were amplified by RNA ligase-mediated 5′ rapid amplification of cDNA ends. In addition, we also conducted contrastive analysis on the genomic location of miRNAs and their potential target genes. Results showed that the order of priority of miRNA–target interaction may be less closely related with their genomic location. These findings could benefit some further study on grapevine functional genomics and will provide new insights into the regulatory mechanisms and evolution of miRNAs in Vitis species.
机译:MicroRNA(miRNA)是单链的,非蛋白质编码的,内源表达的,长度为19至25个核苷酸的小RNA。认识到对葡萄(Vitis vinifera L.)miRNA的全基因组作图缺乏具体和系统的研究,我们进行了Vv-miRNA(V. vinifera miRNA),SB-miRNA(V. vinifera L.' Summer Black'miRNA)和Va-miRNA(V。amurensis Rupr。miRNA)。定位结果表明,位于基因间区域内的许多miRNA具有独立的转录单位。为了进一步验证作图结果和miRNA的存在,成功克隆并测序了12种随机选择的miRNA前体(pre-miRNA)。随后,根据它们在宿主基因中的位置,标记了15个保守的和29个非保守的基因内(内含子,外显子)Vv-miRNA基因,24个非保守的基因内SB-miRNA基因和23个非保守的基因内Va-miRNA基因,以及它们在宿主基因中的位置,并标记了15个MIRNA簇被检测到。有趣的是,五个miRNA对,即Vv-MIR395b和Vv-MIR395c,Vv-MIR482和Vv-MIRC13,Vv-MIR172a和Va-MIR057,SB-MIR024和Vv-MIRC35以及Vv-MIRC36和Va-MIR073分别位于宿主基因GSVIVT01011558001,GSVIVT01008132001,GSVIVT01031524001,GSVIVT01028156001和GSVIVT01024516001中。为了验证靶基因和miRNA指导的切割位点的存在,通过RNA连接酶介导的cDNA末端5'快速扩增,扩增了四个预测的目标信使RNA的3'末端产物。此外,我们还对miRNA及其潜在靶基因的基因组位置进行了对比分析。结果表明,miRNA与靶标相互作用的优先顺序与其基因组位置的联系可能不太紧密。这些发现可能有益于对葡萄功能基因组学的进一步研究,并将为葡萄树种中miRNA的调控机制和进化提供新见解。

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