starBase v2.0: decoding miRNA-ceRNA, miRNA-ncRNA and protein-RNA interaction networks from large-scale CLIP-Seq data
- PMID: 24297251
- PMCID: PMC3964941
- DOI: 10.1093/nar/gkt1248
starBase v2.0: decoding miRNA-ceRNA, miRNA-ncRNA and protein-RNA interaction networks from large-scale CLIP-Seq data
Abstract
Although microRNAs (miRNAs), other non-coding RNAs (ncRNAs) (e.g. lncRNAs, pseudogenes and circRNAs) and competing endogenous RNAs (ceRNAs) have been implicated in cell-fate determination and in various human diseases, surprisingly little is known about the regulatory interaction networks among the multiple classes of RNAs. In this study, we developed starBase v2.0 (http://starbase.sysu.edu.cn/) to systematically identify the RNA-RNA and protein-RNA interaction networks from 108 CLIP-Seq (PAR-CLIP, HITS-CLIP, iCLIP, CLASH) data sets generated by 37 independent studies. By analyzing millions of RNA-binding protein binding sites, we identified ∼9000 miRNA-circRNA, 16 000 miRNA-pseudogene and 285,000 protein-RNA regulatory relationships. Moreover, starBase v2.0 has been updated to provide the most comprehensive CLIP-Seq experimentally supported miRNA-mRNA and miRNA-lncRNA interaction networks to date. We identified ∼10,000 ceRNA pairs from CLIP-supported miRNA target sites. By combining 13 functional genomic annotations, we developed miRFunction and ceRNAFunction web servers to predict the function of miRNAs and other ncRNAs from the miRNA-mediated regulatory networks. Finally, we developed interactive web implementations to provide visualization, analysis and downloading of the aforementioned large-scale data sets. This study will greatly expand our understanding of ncRNA functions and their coordinated regulatory networks.
Figures

Similar articles
-
starBase: a database for exploring microRNA-mRNA interaction maps from Argonaute CLIP-Seq and Degradome-Seq data.Nucleic Acids Res. 2011 Jan;39(Database issue):D202-9. doi: 10.1093/nar/gkq1056. Epub 2010 Oct 30. Nucleic Acids Res. 2011. PMID: 21037263 Free PMC article.
-
Discovery of microRNA regulatory networks by integrating multidimensional high-throughput data.Adv Exp Med Biol. 2013;774:251-66. doi: 10.1007/978-94-007-5590-1_13. Adv Exp Med Biol. 2013. PMID: 23377977
-
Discovering circRNA-microRNA Interactions from CLIP-Seq Data.Methods Mol Biol. 2018;1724:193-207. doi: 10.1007/978-1-4939-7562-4_16. Methods Mol Biol. 2018. PMID: 29322451
-
The multilayered complexity of ceRNA crosstalk and competition.Nature. 2014 Jan 16;505(7483):344-52. doi: 10.1038/nature12986. Nature. 2014. PMID: 24429633 Free PMC article. Review.
-
Roles of ncRNAs as ceRNAs in Gastric Cancer.Genes (Basel). 2021 Jul 2;12(7):1036. doi: 10.3390/genes12071036. Genes (Basel). 2021. PMID: 34356052 Free PMC article. Review.
Cited by
-
Two predicted models based on ceRNAs and immune cells in lung adenocarcinoma.PeerJ. 2021 Mar 23;9:e11029. doi: 10.7717/peerj.11029. eCollection 2021. PeerJ. 2021. PMID: 33828913 Free PMC article.
-
Critical role of SIRT1 upregulation on the protective effect of lncRNA ANRIL against hypoxia/reoxygenation injury in H9c2 cardiomyocytes.Mol Med Rep. 2021 Aug;24(2):547. doi: 10.3892/mmr.2021.12186. Epub 2021 Jun 3. Mol Med Rep. 2021. PMID: 34080028 Free PMC article.
-
Bioinformatics analysis of ferroptosis in spinal cord injury.Neural Regen Res. 2023 Mar;18(3):626-633. doi: 10.4103/1673-5374.350209. Neural Regen Res. 2023. PMID: 36018187 Free PMC article.
-
Next-generation sequencing reveals novel differentially regulated mRNAs, lncRNAs, miRNAs, sdRNAs and a piRNA in pancreatic cancer.Mol Cancer. 2015 Apr 25;14:94. doi: 10.1186/s12943-015-0358-5. Mol Cancer. 2015. PMID: 25910082 Free PMC article.
-
BDE-47, -99, -209 and Their Ternary Mixture Disrupt Glucose and Lipid Metabolism of Hepg2 Cells at Dietary Relevant Concentrations: Mechanistic Insight through Integrated Transcriptomics and Proteomics Analysis.Int J Mol Sci. 2022 Nov 21;23(22):14465. doi: 10.3390/ijms232214465. Int J Mol Sci. 2022. PMID: 36430946 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources