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Genomic Features of Parthenogenetic Animals
Evolution without sex is predicted to impact genomes in numerous ways. Case studies of individual parthenogenetic animals have reported peculiar genomic features that were suggested to be caused by their mode of reproduction, including high heterozygosity, a high abundance of horizontally acquired g...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953838/ https://www.ncbi.nlm.nih.gov/pubmed/32985658 http://dx.doi.org/10.1093/jhered/esaa031 |
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author | Jaron, Kamil S Bast, Jens Nowell, Reuben W Ranallo-Benavidez, T Rhyker Robinson-Rechavi, Marc Schwander, Tanja |
author_facet | Jaron, Kamil S Bast, Jens Nowell, Reuben W Ranallo-Benavidez, T Rhyker Robinson-Rechavi, Marc Schwander, Tanja |
author_sort | Jaron, Kamil S |
collection | PubMed |
description | Evolution without sex is predicted to impact genomes in numerous ways. Case studies of individual parthenogenetic animals have reported peculiar genomic features that were suggested to be caused by their mode of reproduction, including high heterozygosity, a high abundance of horizontally acquired genes, a low transposable element load, or the presence of palindromes. We systematically characterized these genomic features in published genomes of 26 parthenogenetic animals representing at least 18 independent transitions to asexuality. Surprisingly, not a single feature was systematically replicated across a majority of these transitions, suggesting that previously reported patterns were lineage-specific rather than illustrating the general consequences of parthenogenesis. We found that only parthenogens of hybrid origin were characterized by high heterozygosity levels. Parthenogens that were not of hybrid origin appeared to be largely homozygous, independent of the cellular mechanism underlying parthenogenesis. Overall, despite the importance of recombination rate variation for the evolution of sexual animal genomes, the genome-wide absence of recombination does not appear to have had the dramatic effects which are expected from classical theoretical models. The reasons for this are probably a combination of lineage-specific patterns, the impact of the origin of parthenogenesis, and a survivorship bias of parthenogenetic lineages. |
format | Online Article Text |
id | pubmed-7953838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79538382021-03-17 Genomic Features of Parthenogenetic Animals Jaron, Kamil S Bast, Jens Nowell, Reuben W Ranallo-Benavidez, T Rhyker Robinson-Rechavi, Marc Schwander, Tanja J Hered Symposium Articles Evolution without sex is predicted to impact genomes in numerous ways. Case studies of individual parthenogenetic animals have reported peculiar genomic features that were suggested to be caused by their mode of reproduction, including high heterozygosity, a high abundance of horizontally acquired genes, a low transposable element load, or the presence of palindromes. We systematically characterized these genomic features in published genomes of 26 parthenogenetic animals representing at least 18 independent transitions to asexuality. Surprisingly, not a single feature was systematically replicated across a majority of these transitions, suggesting that previously reported patterns were lineage-specific rather than illustrating the general consequences of parthenogenesis. We found that only parthenogens of hybrid origin were characterized by high heterozygosity levels. Parthenogens that were not of hybrid origin appeared to be largely homozygous, independent of the cellular mechanism underlying parthenogenesis. Overall, despite the importance of recombination rate variation for the evolution of sexual animal genomes, the genome-wide absence of recombination does not appear to have had the dramatic effects which are expected from classical theoretical models. The reasons for this are probably a combination of lineage-specific patterns, the impact of the origin of parthenogenesis, and a survivorship bias of parthenogenetic lineages. Oxford University Press 2020-09-28 /pmc/articles/PMC7953838/ /pubmed/32985658 http://dx.doi.org/10.1093/jhered/esaa031 Text en © The American Genetic Association 2020. 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 | Symposium Articles Jaron, Kamil S Bast, Jens Nowell, Reuben W Ranallo-Benavidez, T Rhyker Robinson-Rechavi, Marc Schwander, Tanja Genomic Features of Parthenogenetic Animals |
title | Genomic Features of Parthenogenetic Animals |
title_full | Genomic Features of Parthenogenetic Animals |
title_fullStr | Genomic Features of Parthenogenetic Animals |
title_full_unstemmed | Genomic Features of Parthenogenetic Animals |
title_short | Genomic Features of Parthenogenetic Animals |
title_sort | genomic features of parthenogenetic animals |
topic | Symposium Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953838/ https://www.ncbi.nlm.nih.gov/pubmed/32985658 http://dx.doi.org/10.1093/jhered/esaa031 |
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