Abstract

Simple SummaryRibonucleic acids (RNAs) are generally linear chains of nucleotides which function in many cellular processes, best known in protein biosynthesis. In the last decade, circular RNAs have been discovered which are circularized after their synthesis and differ in important features from linear RNAs. These circular RNAs have meanwhile been implicated in important cellular processes in health and disease. Here, we present a comprehensive database, circ2GO, compiling and analyzing circular RNAs found in lung cancer cell lines providing the data in tables as well as visualizing it in transcript maps and in heatmaps. Importantly, we also provide easy-to-use online tools to find circular forms of genes associated with specific molecular functions, biological processes or cellular components or predict their targeted microRNAs. This resource will enable researchers to rapidly identify circular RNAs relevant for their specific research question.Circular RNAs (circRNAs) play critical roles in a broad spectrum of physiological and pathological processes, including cancer. Here, we provide a comprehensive database—circ2GO—systematically linking circRNAs to the functions and processes of their linear counterparts. circ2GO contains 148,811 circular human RNAs originating from 12,251 genes, which we derived from deep transcriptomics after rRNA depletion in a panel of 60 lung cancer and non-transformed cell lines. The broad circRNA expression dataset is mapped to all isoforms of the respective gene. The data are visualized in transcript maps and in heatmaps, to intuitively display a comprehensive portrait for the abundance of circRNAs across transcripts and cell lines. By integrating gene ontology (GO) information for all genes in our dataset, circ2GO builds a connection between circRNAs and their host genes’ biological functions and molecular mechanisms. Additionally, circ2GO offers target predictions for circRNA—microRNA (miRNA) pairs for 25,166 highly abundant circRNAs from 6578 genes and 897 high-confidence human miRNAs. Visualization, user-friendliness, intuitive and advanced forward and reverse search options, batch processing and download options make circ2GO a comprehensive source for circRNA information to build hypotheses on their function, processes, and miRNA targets.

Highlights

  • Circular RNAs constitute a class of single-stranded RNA with a covalent bond of the 30 -end to the 50 -end by back-splicing

  • Growing evidence shows that circRNAs are widely expressed in vertebrate cells and show tissue-specific and cell type-specific expression patterns. circRNA biogenesis is believed to be regulated by signals in cis, as well as factors acting in trans to govern the context-dependent efficiency of circularization

  • The circRNA dataset was obtained by the sequencing of rRNA-depleted RNAs from 60 lung cell lines with a total of 175 replicates

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Summary

Introduction

Circular RNAs (circRNAs) constitute a class of single-stranded RNA with a covalent bond of the 30 -end to the 50 -end by back-splicing. The covalently closed continuous loop makes circRNAs resistant against degradation by exonucleases, and they have a longer half-life than their linear. CircRNA biogenesis is believed to be regulated by signals in cis, as well as factors acting in trans to govern the context-dependent efficiency of circularization. CircRNAs are often intimately linked to the expression or function of their linear host gene [5,6,7,8]. Even though thousands of circRNAs have been discovered, the underlying mechanisms regulating their biogenesis, function, degradation, and cellular localization remains unclear in most cases

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