Related Experiment Video
Updated: Jan 6, 2026

10:27
In Silico Identification and Characterization of circRNAs During Host-Pathogen Interactions
Published on: October 21, 2022
1.9K
CircAI: a comprehensive database of CircRNA associated with A-to-I RNA editing
Yulan Wang1,2, Lingxiao Zou1, Jian Zhao1
1Department of Biomedical Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing 211106, China.
Database : the Journal of Biological Databases and Curation
|November 22, 2025
Summary
RNA editing, a key process altering RNA, has many unknown functions, especially in circular RNAs (circRNAs). We created CircAI, a database detailing circRNA editing sites and predicting their functional impacts across species.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- RNA editing, particularly adenosine-to-inosine (A-to-I) modification, is a widespread posttranscriptional event with significant functional roles.
- Over 2 million A-to-I RNA editing sites are known in mammals, but their functional implications, especially in noncoding regions and circular RNAs (circRNAs), remain largely unexplored.
Purpose of the Study:
- To comprehensively analyze A-to-I RNA editing sites in circRNAs across multiple species.
- To develop a centralized database, CircAI, integrating circRNA editing data with functional predictions.
- To provide a resource for investigating the functional consequences of RNA editing in circRNAs.
Main Methods:
- In-depth analysis of A-to-I editing sites in circRNAs from eight species: Homo sapiens, Mus musculus, Macaca mulatta, Gallus gallus, Rattus norvegicus, Oryctolagus cuniculus, Sus scrofa, and Danio rerio.
- Integration of gathered data into the CircAI database.
- Development of functional prediction modules within CircAI, including coding potential, miRNA interactions, secondary structures, and RNA editing quantitative trait loci (edQTL).
Main Results:
- Identification and compilation of multispecies circRNA editing data.
- Establishment of CircAI, the first database combining circRNA editing information with functional predictions.
- Implementation of user-friendly tools for exploring predicted functional impacts of circRNA editing.
Conclusions:
- CircAI provides a valuable resource for understanding the functional significance of RNA editing in circRNAs.
- The database facilitates research into the roles of circRNA editing in biological processes and disease.
- Further exploration of circRNA editing through CircAI can uncover novel regulatory mechanisms.
Related Concept Videos
RNA Editing
9.7K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.7K
RNA Interference
27.7K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
27.7K
Experimental RNAi
7.2K
RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
7.2K
Nonsense-mediated mRNA Decay
11.6K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
11.6K
RNA-seq
11.7K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
11.7K
piRNA - Piwi-interacting RNAs
7.4K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
7.4K

