4.6 Article

Large-Scale Profiling of RBP-circRNA Interactions from Public CLIP-Seq Datasets

期刊

GENES
卷 11, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/genes11010054

关键词

Circ-RNA; CLIP-Seq; RBP

资金

  1. National Institutes of Health (NIH) [1R01GM115473, P50CA070907, R03ES026397, P50CA196516]
  2. Cancer Prevention and Research Institute of Texas [RP120732]

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Circular RNAs are a special type of RNA that has recently attracted a lot of research interest in studying its formation and function. RNA binding proteins (RBPs) that bind circRNAs are important in these processes, but have been relatively less studied. CLIP-Seq technology has been invented and applied to profile RBP-RNA interactions on the genome-wide scale. While mRNAs are usually the focus of CLIP-Seq experiments, RBP-circRNA interactions could also be identified through specialized analysis of CLIP-Seq datasets. However, many technical difficulties are involved in this process, such as the usually short read length of CLIP-Seq reads. In this study, we created a pipeline called Clirc specialized for profiling circRNAs in CLIP-Seq data and analyzing the characteristics of RBP-circRNA interactions. In conclusion, to our knowledge, this is one of the first studies to investigate circRNAs and their binding partners through repurposing CLIP-Seq datasets, and we hope our work will become a valuable resource for future studies into the biogenesis and function of circRNAs.

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