...
首页> 外文期刊>BMC Genomics >Computational prediction and experimental validation of evolutionarily conserved microRNA target genes in bilaterian animals
【24h】

Computational prediction and experimental validation of evolutionarily conserved microRNA target genes in bilaterian animals

机译:双边动物中进化保守的microRNA靶基因的计算预测和实验验证

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Background In many eukaryotes, microRNAs (miRNAs) bind to complementary sites in the 3'-untranslated regions (3'-UTRs) of target messenger RNAs (mRNAs) and regulate their expression at the stage of translation. Recent studies have revealed that many miRNAs are evolutionarily conserved; however, the evolution of their target genes has yet to be systematically characterized. We sought to elucidate a set of conserved miRNA/target-gene pairs and to analyse the mechanism underlying miRNA-mediated gene regulation in the early stage of bilaterian evolution. Results Initially, we extracted five evolutionarily conserved miRNAs (let-7, miR-1, miR-124, miR-125/lin-4, and miR-34) among five diverse bilaterian animals. Subsequently, we designed a procedure to predict evolutionarily conserved miRNA/target-gene pairs by introducing orthologous gene information. As a result, we extracted 31 orthologous miRNA/target-gene pairs that were conserved among at least four diverse bilaterian animals; the prediction set showed prominent enrichment of orthologous miRNA/target-gene pairs that were verified experimentally. Approximately 84% of the target genes were regulated by three miRNAs (let-7, miR-1, and miR-124) and their function was classified mainly into the following categories: development, muscle formation, cell adhesion, and gene regulation. We used a reporter gene assay to experimentally verify the downregulation of six candidate pairs (out of six tested pairs) in HeLa cells. Conclusions The application of our new method enables the identification of 31 miRNA/target-gene pairs that were expected to have been regulated from the era of the common bilaterian ancestor. The downregulation of all six candidate pairs suggests that orthologous information contributed to the elucidation of the primordial set of genes that has been regulated by miRNAs; it was also an efficient tool for the elimination of false positives from the predicted candidates. In conclusion, our study identified potentially important miRNA-target pairs that were evolutionarily conserved throughout diverse bilaterian animals and that may provide new insights into early-stage miRNA functions.
机译:背景技术在许多真核生物中,microRNA(miRNA)结合至目标信使RNA(mRNA)的3'-非翻译区(3'-UTR)中的互补位点,并在翻译阶段调节其表达。最近的研究表明,许多miRNA在进化上是保守的。然而,其靶基因的进化尚未系统地表征。我们试图阐明一组保守的miRNA /靶基因对,并分析在Bilaterian进化的早期阶段,miRNA介导的基因调控的机制。结果最初,我们从五种不同的双边动物中提取了五个进化保守的miRNA(let-7,miR-1,miR-124,miR-125 / lin-4和miR-34)。随后,我们设计了一种程序,通过引入直系同源基因信息来预测进化保守的miRNA /靶基因对。结果,我们提取了31个直系同源miRNA /靶标基因对,它们在至少四只不同的双边动物中是保守的。该预测集显示了直系同源miRNA /靶标基因对的显着富集,已通过实验验证。大约84%的目标基因受三种miRNA(let-7,miR-1和miR-124)调控,其功能主要分为以下几类:发育,肌肉形成,细胞粘附和基因调控。我们使用了一种记者基因检测法,通过实验验证了HeLa细胞中六种候选对(六种测试对中)的下调。结论我们新方法的应用使得能够鉴定31种miRNA /靶基因对,这些对有望从普通双祖先时代开始受到调控。所有六个候选对的表达下调表明直系同源信息有助于阐明已受miRNA调控的原始基因组。这也是从预测的候选人中消除误报的有效工具。总而言之,我们的研究确定了潜在的重要miRNA-靶标对,这些对在整个不同的双侧动物中都得到了进化保守,并可能为早期miRNA的功能提供新的见解。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号