Abstract
In animals, the most common type of RNA editing is the deamination of adenosines (A) into inosines (I). Because inosines basepair with cytosines (C), they are interpreted as guanosines (G) by the cellular machinery and genomically encoded G alleles at edited sites mimic the function of edited RNAs. The contribution of this hardwiring effect on genome evolution remains obscure. We looked for population genomics signatures of adaptive evolution associated with A-to-I RNA edited sites in humans and Drosophila melanogaster. We found that single nucleotide polymorphisms at edited sites occur 3 (humans) to 15 times (Drosophila) more often than at unedited sites, the nucleotide G is virtually the unique alternative allele at edited sites and G alleles segregate at higher frequency at edited sites than at unedited sites. Our study reveals that a significant fraction of coding synonymous and nonsynonymous as well as silent and intergenic A-to-I RNA editing sites are likely adaptive in the distantly related human and Drosophila lineages.
Original language | English |
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Pages (from-to) | 345-357 |
Number of pages | 13 |
Journal | Genome Biology and Evolution |
Volume | 12 |
Issue number | 4 |
DOIs | |
State | Published - 1 Apr 2020 |
Bibliographical note
Publisher Copyright:© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.
Funding
We thank Angela M. Hancock and Michael DeGiorgio for valuable comments and suggestions, Nadia Singh for providing data, and Jennifer Gage for proofreading the manuscript. Funded by Austrian Science Foundation grant SFB F43-13 and P26882 (to M.J.), Israel Science Foundation grant 379/12 (to E.E.), and Australian Research Council grant DE180100883 (to C.D.H.).
Funders | Funder number |
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Australian Research Council | DE180100883 |
Austrian Science Fund | P26882, SFB F43-13 |
Israel Science Foundation | 379/12 |
Keywords
- Drosophila
- Human
- Natural selection
- RNA editing