spongeScan: A web for detecting microRNA binding elements in lncRNA sequences

被引:101
作者
Furio-Tari, Pedro [1 ]
Tarazona, Sonia [1 ,2 ]
Gabaldon, Toni [3 ,4 ,5 ]
Enright, Anton J. [6 ]
Conesa, Ana [1 ,7 ]
机构
[1] CIPF, Genom Gene Express Lab, Valencia 46012, Spain
[2] Univ Politecn Valencia, Dept Appl Stat Operat Res & Qual, E-46022 Valencia, Spain
[3] Ctr Genom Regulat CRG, Barcelona 08003, Spain
[4] UPF, Barcelona 08002, Spain
[5] ICREA, Barcelona 08010, Spain
[6] EMBL European Bioinformat Inst, Wellcome Trust Genome Campus, Cambridge CB4 1GU, England
[7] Univ Florida, Microbiol & Cell Sci, IFAS, Gainesville, FL 32611 USA
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1093/nar/gkw443
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-coding RNA transcripts such as microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) are important genetic regulators. However, the functions of many of these transcripts are still not clearly understood. Recently, it has become apparent that there is significant crosstalk between miRNAs and lncRNAs and that this creates competition for binding between the miRNA, a lncRNA and other regulatory targets. Indeed, various competitive endogenous RNAs (ceRNAs) have already been identified where a lncRNA acts by sequestering miRNAs. This implies the down-regulation in the interaction of the miRNAs with their mRNA targets, what has been called a sponge effect. Multiple approaches exist for the prediction of miRNA targets in mRNAs. However, few methods exist for the prediction of miRNA response elements (MREs) in lncRNAs acting as ceRNAs (sponges). Here, we present spongeScan (http://spongescan.rc.ufl.edu), a graphical web tool to compute and visualize putative MREs in lncRNAs, along with different measures to assess their likely behavior as ceRNAs.
引用
收藏
页码:W176 / W180
页数:5
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