Analysis of common targets for circular RNAs

被引:21
作者
Lin, Ya-Chi [1 ,2 ]
Lee, Yueh-Chun [3 ,4 ]
Chang, Kai-Li [5 ]
Hsiao, Kuei-Yang [6 ,7 ,8 ,9 ]
机构
[1] Natl Chung Hsing Univ, Coll Agr & Nat Resources, Dept Plant Pathol, Taichung 40227, Taiwan
[2] Asia Univ, Dept Biotechnol, Taichung 41354, Taiwan
[3] Chung Shan Med Univ Hosp, Dept Radiat Oncol, Taichung 40201, Taiwan
[4] Chung Shan Med Univ, Sch Med, Taichung 40201, Taiwan
[5] Natl Cheng Kung Univ, Dept Physiol, Tainan 70101, Taiwan
[6] Natl Chung Hsing Univ, Coll Life Sci, Inst Biochem, Taichung 40227, Taiwan
[7] Natl Chung Hsing Univ, Coll Life Sci, Program Translat Med, Taichung 40227, Taiwan
[8] Natl Chung Hsing Univ, Coll Life Sci, Rong Hsing Res Ctr Translat Med, Taichung 40227, Taiwan
[9] Natl Chung Hsing Univ, Coll Agr & Nat Resources, Bachelor Program Biotechnol, Taichung 40227, Taiwan
关键词
Circular RNA; microRNA; Common targets; miRNA sponge; NONCODING RNA; IDENTIFICATION; DATABASE;
D O I
10.1186/s12859-019-2966-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundThe studies of functions of circular RNAs (circRNAs) are heavily focused on the regulation of gene expression through interactions with multiple miRNAs. However, the number of predicted target genes is typically overwhelming due to the synergistic complexity caused by two factors the binding of multiple miRNAs to a circRNA and the existence of multiple targets for each miRNA. Analysis of common targets (ACT) was designed to facilitate the identification of potential circRNA targets.ResultsWe demonstrated the feasibility of the proposed feature/measurement to assess which genes are more likely to be regulated by circRNAs with given sequences by calculating the level of co-regulation by multiple miRNAs. The web service is made freely available at http://lab-x-omics.nchu.edu.tw/ACT_Server.ConclusionsACT allows users to identify potential circRNA-regulated genes and their associated pathways for further investigation.
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页数:6
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