Jiu Songtao, Zhu Xudong, Wang Jian, Zhang Cheng, Mu Qian, Wang Chen, Fang Jinggui
College of Horticulture, Nanjing Agricultural Univ., Nanjing City, Jiangsu Province, PR China.
Plant Genome. 2015 Jul;8(2):eplantgenome2014.12.0091. doi: 10.3835/plantgenome2014.12.0091.
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.
微小RNA(miRNA)是单链、非蛋白质编码、内源性表达的小RNA,长度为19至25个核苷酸。鉴于缺乏对葡萄(Vitis vinifera L.)miRNA全基因组图谱的特异性和系统性研究,我们开展了酿酒葡萄miRNA(Vv-miRNA)、‘夏黑’葡萄miRNA(SB-miRNA)和山葡萄miRNA(Va-miRNA)的全基因组图谱绘制。图谱绘制结果显示,许多位于基因间区域的miRNA具有独立的转录单元。为进一步验证图谱绘制结果及miRNA的存在,我们成功克隆并测序了12个随机选择的miRNA前体(pre-miRNA)。随后,根据其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,并检测到15个miRNA簇。有趣的是,五对miRNA,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,分别聚集在宿主基因GSVIVT01011558001、GSVIVT01008132001、GSVIVT01031524001、GSVIVT01028156001和GSVIVT01024516001中。为验证靶基因的存在及miRNA引导的切割位点,通过RNA连接酶介导的5' cDNA末端快速扩增,扩增了四个预测靶信使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-靶标相互作用的优先顺序可能与其基因组位置的相关性较小。这些发现将有助于葡萄功能基因组学的进一步研究,并为葡萄属物种中miRNA的调控机制和进化提供新的见解。