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Identification and Characterization of Novel miRNAs in Chlamydomonas reinhardtii by Computational Methods

机译:用计算方法鉴定和鉴定莱茵衣藻中新型miRNA。

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Background: MicroRNAs (miRNAs) are endogenous small non-coding RNAs with 18-24 nucleotides in length, which have important roles in post-transcriptional gene regulation. The resemblance of miRNA biogenesis in unicellular green algae and those in plants suggests probable evolutionary conserved pathways. This conservation provides a ground towards prediction of new homologs via computational biology. Methods: Here, conserved miRNA genes in Chlamydomonas reinhardtii and plants were examined through homology alignment. Previously known and unique plant miRNAs were BLASTed against expressed sequence tags (ESTs) and genomic survey sequences (GSSs) of C. reinhardtii. All candidate sequences with appropriate fold back structures were screened according to a series of miRNA filtering criteria. Results: Homologous miRNAs (17), belonging to 9 miRNA gene families were predicted. Interestingly and for the first time, a miRNA family of genes was localized to chloroplast. Again and for the first time, here we report identification of C. reinhardtii miRNA orthologs in plants and animals. miRNA target genes were identified based on their sequence complementarities to the respective miRNAs using psRNATarget against C. reinhardtii, Unigene, and DFCI Gene Index (CHRGI). Totally, 152 potential target sites were identified. From the predicted miRNAs, 7 miRNAs had no target sequence in C. reinhardtii protein coding genes. Conclusion: Identifying miRNA and their target transcript(s) would be useful for other research concerned with the function and regulatory mechanisms of C. reinhardtii miRNAs and helps researchers to better understand the nature of its extensive metabolic flexibility and environmental compatibility to survive in distinct environmental niches and nutrient availability.
机译:背景:MicroRNA(miRNA)是内源的小非编码RNA,长度为18-24个核苷酸,在转录后基因调控中起重要作用。单细胞绿藻和植物中miRNA生物发生的相似性表明可能是进化保守的途径。这种保护为通过计算生物学预测新的同源物提供了基础。方法:在这里,通过同源性比对检查了莱茵衣藻和植物中的保守miRNA基因。将先前已知和独特的植物miRNA进行了针对莱茵衣藻的表达序列标签(EST)和基因组调查序列(GSS)的BLAST处理。根据一系列miRNA过滤标准,筛选出具有适当折返结构的所有候选序列。结果:预测到属于9个miRNA基因家族的同源miRNA(17)。有趣的是,miRNA基因家族首次定位于叶绿体。再次,这是第一次,我们在这里报告了在植物和动物中识别莱茵衣原体miRNA直系同源物的过程。使用针对reinhardtii,Unigene和DFCI基因索引(CHRGI)的psRNATarget,基于与各个miRNA的序列互补性来鉴定miRNA靶基因。总共确定了152个潜在目标站点。从预测的miRNA中,有7个miRNA在莱茵衣藻蛋白编码基因中没有靶序列。结论:鉴定miRNA及其靶转录本可用于与莱茵衣藻miRNA的功能和调控机制有关的其他研究,并有助于研究人员更好地了解其广泛的代谢灵活性和环境相容性,以在不同的环境中生存生态位和养分供应。

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