GN Ramachandran Knowledge Center for Genome Informatics, CSIR-Institute of Genomics and Integrative Biology (CSIR-IGIB), Delhi, India.
PLoS One. 2013;8(2):e53823. doi: 10.1371/journal.pone.0053823. Epub 2013 Feb 6.
Long noncoding RNAs (lncRNAs) are a recently discovered class of non-protein coding RNAs, which have now increasingly been shown to be involved in a wide variety of biological processes as regulatory molecules. The functional role of many of the members of this class has been an enigma, except a few of them like Malat and HOTAIR. Little is known regarding the regulatory interactions between noncoding RNA classes. Recent reports have suggested that lncRNAs could potentially interact with other classes of non-coding RNAs including microRNAs (miRNAs) and modulate their regulatory role through interactions. We hypothesized that lncRNAs could participate as a layer of regulatory interactions with miRNAs. The availability of genome-scale datasets for Argonaute targets across human transcriptome has prompted us to reconstruct a genome-scale network of interactions between miRNAs and lncRNAs.
We used well characterized experimental Photoactivatable-Ribonucleoside-Enhanced Crosslinking and Immunoprecipitation (PAR-CLIP) datasets and the recent genome-wide annotations for lncRNAs in public domain to construct a comprehensive transcriptome-wide map of miRNA regulatory elements. Comparative analysis revealed that in addition to targeting protein-coding transcripts, miRNAs could also potentially target lncRNAs, thus participating in a novel layer of regulatory interactions between noncoding RNA classes. Furthermore, we have modeled one example of miRNA-lncRNA interaction using a zebrafish model. We have also found that the miRNA regulatory elements have a positional preference, clustering towards the mid regions and 3' ends of the long noncoding transcripts. We also further reconstruct a genome-wide map of miRNA interactions with lncRNAs as well as messenger RNAs.
This analysis suggests widespread regulatory interactions between noncoding RNAs classes and suggests a novel functional role for lncRNAs. We also present the first transcriptome scale study on miRNA-lncRNA interactions and the first report of a genome-scale reconstruction of a noncoding RNA regulatory interactome involving lncRNAs.
长非编码 RNA(lncRNA)是一类新发现的非蛋白编码 RNA,现已越来越多地被证明作为调节分子参与多种生物学过程。该类别的许多成员的功能作用一直是个谜,除了少数几个,如 Malat 和 HOTAIR。关于非编码 RNA 类别之间的调节相互作用知之甚少。最近的报告表明,lncRNA 可能与其他非编码 RNA 类别(包括 microRNA(miRNA))相互作用,并通过相互作用调节其调节作用。我们假设 lncRNA 可以作为 miRNA 调节相互作用的一层参与。Argonaute 靶标在人类转录组中的全基因组数据集的可用性促使我们构建了 miRNA 和 lncRNA 之间全基因组规模相互作用的网络。
我们使用了经过充分表征的实验 Photoactivatable-Ribonucleoside-Enhanced Crosslinking 和 Immunoprecipitation(PAR-CLIP)数据集,以及公共领域中最近的 lncRNA 全基因组注释,构建了 miRNA 调节元件的综合全转录组图谱。比较分析表明,除了靶向蛋白质编码转录物外,miRNA 还可能靶向 lncRNA,从而参与非编码 RNA 类别之间的新型调节相互作用。此外,我们使用斑马鱼模型模拟了 miRNA-lncRNA 相互作用的一个示例。我们还发现,miRNA 调节元件具有位置偏好性,聚类在长非编码转录物的中部和 3' 端附近。我们还进一步重建了 miRNA 与 lncRNA 以及信使 RNA 之间的全基因组图谱。
这项分析表明非编码 RNA 类别之间存在广泛的调节相互作用,并为 lncRNA 的新功能作用提供了依据。我们还展示了 miRNA-lncRNA 相互作用的第一个转录组规模研究,以及涉及 lncRNA 的第一个非编码 RNA 调节相互作用组的全基因组重建报告。