Cargando…
A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals
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....
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186786/ https://www.ncbi.nlm.nih.gov/pubmed/32145015 http://dx.doi.org/10.1093/gbe/evaa046 |
_version_ | 1783527029049655296 |
---|---|
author | Popitsch, Niko Huber, Christian D Buchumenski, Ilana Eisenberg, Eli Jantsch, Michael von Haeseler, Arndt Gallach, Miguel |
author_facet | Popitsch, Niko Huber, Christian D Buchumenski, Ilana Eisenberg, Eli Jantsch, Michael von Haeseler, Arndt Gallach, Miguel |
author_sort | Popitsch, Niko |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7186786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71867862020-05-01 A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals Popitsch, Niko Huber, Christian D Buchumenski, Ilana Eisenberg, Eli Jantsch, Michael von Haeseler, Arndt Gallach, Miguel Genome Biol Evol Research Article 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. Oxford University Press 2020-03-07 /pmc/articles/PMC7186786/ /pubmed/32145015 http://dx.doi.org/10.1093/gbe/evaa046 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Popitsch, Niko Huber, Christian D Buchumenski, Ilana Eisenberg, Eli Jantsch, Michael von Haeseler, Arndt Gallach, Miguel A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals |
title | A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals |
title_full | A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals |
title_fullStr | A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals |
title_full_unstemmed | A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals |
title_short | A-to-I RNA Editing Uncovers Hidden Signals of Adaptive Genome Evolution in Animals |
title_sort | a-to-i rna editing uncovers hidden signals of adaptive genome evolution in animals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186786/ https://www.ncbi.nlm.nih.gov/pubmed/32145015 http://dx.doi.org/10.1093/gbe/evaa046 |
work_keys_str_mv | AT popitschniko atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals AT huberchristiand atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals AT buchumenskiilana atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals AT eisenbergeli atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals AT jantschmichael atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals AT vonhaeselerarndt atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals AT gallachmiguel atoirnaeditinguncovershiddensignalsofadaptivegenomeevolutioninanimals |