Related Experiment Video
Updated: Jan 17, 2026

08:50
A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
2.9K
On the origin, evolution, and maintenance of RNA editing
Yuange Duan1, Qi Cao2, Qiuhua Xie1
1Department of Entomology and State Key Laboratory of Agricultural and Forestry Biosecurity, MOA Key Lab of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University, Beijing 100193, China.
Nucleic Acids Research
|September 24, 2025
Summary
RNA editing may have originated as a defense against mobile genetic elements (MGEs). This review explores RNA editing
Area of Science:
- Molecular Biology
- Evolutionary Biology
- Genetics
Background:
- RNA editing is a crucial post-transcriptional modification.
- Its evolutionary origins are debated, with recent focus on defense against mobile genetic elements (MGEs).
Purpose of the Study:
- To examine the role of RNA editing in suppressing or tolerating transposable element (TE) proliferation.
- To explore the mechanistic and theoretical underpinnings of RNA editing's functions.
- To integrate the mobile genetic element (MGE) hypothesis with other proposed roles of RNA editing.
Main Methods:
- Review of existing literature and theoretical frameworks.
- Analysis of constructive neutral evolution (CNE) theory in the context of RNA editing.
- Examination of specific A-to-I recoding sites and their evolutionary maintenance.
Main Results:
- RNA editing may function as a defense mechanism against MGEs.
- Constructive neutral evolution (CNE) signals are observed at specific RNA editing sites.
- Certain A-to-I recoding sites are selectively maintained for regulatory purposes, not replaced by genomic G.
Conclusions:
- While an MGE-related origin for RNA editing is plausible, it is not the sole explanation.
- RNA editing serves multiple critical functions, including proteome diversification and mutation correction.
- A broader perspective encompassing diverse roles is essential for understanding RNA editing.
Related Concept Videos
RNA Editing
9.8K
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...
9.8K
Bacterial RNA Polymerase
32.5K
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...
32.5K
RNA Stability
35.6K
Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
35.6K
Pre-mRNA Processing: Modification of pre-mRNA Ends
13.8K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
13.8K
Bacterial Transcription
35.7K
RNA polymerase (RNAP) carries out DNA-dependent RNA synthesis in both bacteria and eukaryotes. Bacteria do not have a membrane-bound nucleus. So, transcription and translation occur simultaneously, on the same DNA template.
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
35.7K
pre-mRNA Processing
57.1K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
57.1K

