Related Experiment Video
Updated: Dec 13, 2025

08:25
Identification of Circular RNAs using RNA Sequencing
Published on: November 14, 2019
12.6K
In-Depth Analysis Reveals Production of Circular RNAs from Non-Coding Sequences
Annie Robic1, Julie Demars1, Christa Kühn2,3
1GenPhySE, Université de Toulouse, INRAE, ENVT, 31326 Castanet Tolosan, France.
Cells
|August 6, 2020
Summary
This study characterizes non-canonical circular RNAs (circRNAs), revealing most originate from non-coding sequences, not just back splicing. We identified novel circRNA types from intronic and mono-exonic non-coding genes.
Area of Science:
- Genomics
- RNA Biology
- Bioinformatics
Background:
- Circular RNAs (circRNAs) are crucial regulatory molecules.
- Total RNA sequencing after ribosomal depletion is standard for circRNA research.
- Non-canonical circRNAs, including those from non-coding genes, are less understood.
Purpose of the Study:
- To characterize non-canonical circRNAs, specifically those not from back splicing and those produced by non-coding genes.
- To investigate the origins and types of non-canonical circRNAs in porcine testis.
Main Methods:
- Analysis of total RNA sequencing data from porcine testis.
- Identification and classification of circRNAs based on junction reads and genomic origin.
- Focus on intron-derived and mono-exonic circRNAs.
Main Results:
- Canonical circRNAs have minimal contribution from long non-coding genes.
- Non-canonical circRNAs arise from intronic sequences (lariat-derived circRNAs, intron circles) and mono-exonic genes.
- A novel type, sub-exonic circRNAs, was identified from mono-exonic genes, including the ribozyme RNA RNase_MRP.
- Intronic circRNAs from ATXN2L suggest a potential new non-coding gene (stable intronic sequence RNA).
Conclusions:
- Most non-canonical circRNAs originate from non-coding sequences.
- Non-coding genes are a significant source of diverse circRNA structures.
- The study highlights the complexity of circRNA biogenesis beyond canonical back splicing.
Related Concept Videos
RNA-seq
11.5K
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...
11.5K
Ribosomal RNA Synthesis
14.3K
Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
14.3K
Ribosome Profiling
4.0K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
4.0K
lncRNA - Long Non-coding RNAs
9.6K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
9.6K
Bacterial RNA Polymerase
32.1K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
32.1K
RACE - Rapid Amplification of cDNA Ends
6.9K
Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
6.9K

