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Genome-wide identification and characterization of microRNA genes and their targets in large yellow croaker (Larimichthys crocea)

机译:大黄克拉克(Larimichthys Crocea)的微小瘤基因及其目标的基因组鉴定及其靶向

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MicroRNAs (miRNAs or miRs) are a class of non -coding RNAs of 20-25 nucleotides (nt) in length, which regulates the expression of gene in eukaryotic organism. Studies has been confirmed that miRNA plays an important role in various biological and metabolic processes in both animals and plants. Predicting new miRNAs by computer based homology search analysis is an effective way to discover novel miRNAs. Though a large number of miRNAs have been reported in many fish species, reports of miRNAs in large yellow croaker (L crocea) are limited especially via the computational-based approaches. In this paper, a method of comparative genomic approach by computational genomic homology based on the conservation of miRNA sequences and the stem-loop hairpin secondary structures of miRNAs was adopted. A total of 199 potential miRNAs were predicted representing 81 families. 12 of them were chose to be validated by real time RT-PCR, apart from miR-7132b-5p which was not detected. Results indicated that the prediction method that we used to identify the miRNAs was effective. Furthermore, 948 potential target genes were predicted. Gene ontology (GO) analysis revealed that 175, 287, and 486 target genes were involved in cellular components, biological processes and molecular functions, respectively. Overall, our findings provide a first computational identification and characterization of L crocea miRNAs and their potential targets in functional analysis, and will be useful in laying the foundation for further characterization of their role in the regulation of diversity of physiological processes. (C) 2015 Elsevier B.V. All rights reserved.
机译:MicroRNAS(miRNA或mirs)是一类长度为20-25个核苷酸(NT)的不编码RNA,其调节基因在真核生物中的表达。研究已经证实,MiRNA在动物和植物中的各种生物和代谢过程中起重要作用。通过基于计算机的同源性搜索分析预测新的miRNA是探索小说MiRNA的有效方法。虽然在许多鱼类中报告了大量的miRNA,但大黄色克罗克克(L Crocea)中的MiRNA报告特别是通过基于计算的方法有限的限制。本文采用基于MiRNA序列守恒计算基因组同源的比较基因组方法的方法及MiRNA的茎环发夹二次结构。预计总共有199个潜在的miRNA,代表了81个家庭。其中12种被实时RT-PCR验证,除了未检测到的miR-7132b-5p。结果表明,我们用于识别miRNA的预测方法是有效的。此外,预测了948个潜在的靶基因。基因本体学(GO)分析显示,参与细胞组分,生物过程和分子官能的175,287和486个靶基因。总体而言,我们的研究结果提供了L鳄鱼MiRNA的第一个计算鉴定和表征,并且它们在功能分析中的潜在目标,并将用于奠定基础,以进一步表征其在生理过程多样性中的作用。 (c)2015 Elsevier B.v.保留所有权利。

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