Abstract
BackgroundAdenosine to inosine (A-to-I) RNA editing is a post-transcriptional modification catalyzed by the ADAR (adenosine deaminase that acts on RNA) enzymes, which are ubiquitously expressed among metazoans. Technical requirements have limited systematic mapping of editing sites to a small number of organisms. Thus, the extent of editing across the metazoan lineage is largely unknown.ResultsHere, we apply a computational procedure to search for RNA-sequencing reads containing clusters of editing sites in 21 diverse organisms. Clusters of editing sites are abundant in repetitive genomic regions that putatively form double-stranded RNA (dsRNA) structures and are rarely seen in coding regions. The method reveals a considerable variation in hyper-editing levels across species, which is partly explained by differences in the potential of sequences to form dsRNA structures and the variability of ADAR proteins. Several commonly used model animals exhibit low editing levels and editing levels in primates is not exceptionally high, as previously suggested.ConclusionsEditing by ADARs is highly prevalent across the Metazoa, mostly targeting dsRNA structures formed by genomic repeats. The degree to which the transcriptome of a given species undergoes hyper-editing is governed by the repertoire of repeats in the underlying genome. The strong association of RNA editing with the long dsRNA regions originating from non-coding repetitive elements is contrasted by the almost non-existing signal seen in coding regions. Hyper-edited regions are rarely expressed in a non-edited form. These results support the notion that the main role of ADAR is to suppress the cellular response to endogenous dsRNA structures.
Highlights
Adenosine to inosine (A-to-I) RNA editing is a post-transcriptional modification catalyzed by the adenosine deaminases acting on RNA (ADAR) enzymes, which are ubiquitously expressed among metazoans
Adenosine-to-inosine (A-to-I) RNA editing is a fundamental post-transcriptional gene regulatory mechanism, diversifying the transcriptome of Metazoa [1, 2]. It is catalyzed by the family of adenosine deaminases acting on RNA (ADAR) enzymes [3] and is considered to be more active in the brain [4]
We have looked at Saccharomyces cerevisiae and Arabidopsis thaliana that do not contain the ADAR editing enzymes and verified that they do not show any evidence for A-to-I hyper-editing
Summary
Adenosine to inosine (A-to-I) RNA editing is a post-transcriptional modification catalyzed by the ADAR (adenosine deaminase that acts on RNA) enzymes, which are ubiquitously expressed among metazoans. Technical requirements have limited systematic mapping of editing sites to a small number of organisms. Adenosine-to-inosine (A-to-I) RNA editing is a fundamental post-transcriptional gene regulatory mechanism, diversifying the transcriptome of Metazoa [1, 2]. It is catalyzed by the family of adenosine deaminases acting on RNA (ADAR) enzymes [3] and is considered to be more active in the brain [4].
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