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Hybridization promotes asexual reproduction in Caenorhabditis nematodes

Although most unicellular organisms reproduce asexually, most multicellular eukaryotes are obligately sexual. This implies that there are strong barriers that prevent the origin or maintenance of asexuality arising from an obligately sexual ancestor. By studying rare asexual animal species we can ga...

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Autores principales: Lamelza, Piero, Young, Janet M., Noble, Luke M., Caro, Lews, Isakharov, Arielle, Palanisamy, Meenakshi, Rockman, Matthew V., Malik, Harmit S., Ailion, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946170/
https://www.ncbi.nlm.nih.gov/pubmed/31841515
http://dx.doi.org/10.1371/journal.pgen.1008520
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author Lamelza, Piero
Young, Janet M.
Noble, Luke M.
Caro, Lews
Isakharov, Arielle
Palanisamy, Meenakshi
Rockman, Matthew V.
Malik, Harmit S.
Ailion, Michael
author_facet Lamelza, Piero
Young, Janet M.
Noble, Luke M.
Caro, Lews
Isakharov, Arielle
Palanisamy, Meenakshi
Rockman, Matthew V.
Malik, Harmit S.
Ailion, Michael
author_sort Lamelza, Piero
collection PubMed
description Although most unicellular organisms reproduce asexually, most multicellular eukaryotes are obligately sexual. This implies that there are strong barriers that prevent the origin or maintenance of asexuality arising from an obligately sexual ancestor. By studying rare asexual animal species we can gain a better understanding of the circumstances that facilitate their evolution from a sexual ancestor. Of the known asexual animal species, many originated by hybridization between two ancestral sexual species. The balance hypothesis predicts that genetic incompatibilities between the divergent genomes in hybrids can modify meiosis and facilitate asexual reproduction, but there are few instances where this has been shown. Here we report that hybridizing two sexual Caenorhabditis nematode species (C. nouraguensis females and C. becei males) alters the normal inheritance of the maternal and paternal genomes during the formation of hybrid zygotes. Most offspring of this interspecies cross die during embryogenesis, exhibiting inheritance of a diploid C. nouraguensis maternal genome and incomplete inheritance of C. becei paternal DNA. However, a small fraction of offspring develop into viable adults that can be either fertile or sterile. Fertile offspring are produced asexually by sperm-dependent parthenogenesis (also called gynogenesis or pseudogamy); these progeny inherit a diploid maternal genome but fail to inherit a paternal genome. Sterile offspring are hybrids that inherit both a diploid maternal genome and a haploid paternal genome. Whole-genome sequencing of individual viable worms shows that diploid maternal inheritance in both fertile and sterile offspring results from an altered meiosis in C. nouraguensis oocytes and the inheritance of two randomly selected homologous chromatids. We hypothesize that hybrid incompatibility between C. nouraguensis and C. becei modifies maternal and paternal genome inheritance and indirectly induces gynogenetic reproduction. This system can be used to dissect the molecular mechanisms by which hybrid incompatibilities can facilitate the emergence of asexual reproduction.
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spelling pubmed-69461702020-01-17 Hybridization promotes asexual reproduction in Caenorhabditis nematodes Lamelza, Piero Young, Janet M. Noble, Luke M. Caro, Lews Isakharov, Arielle Palanisamy, Meenakshi Rockman, Matthew V. Malik, Harmit S. Ailion, Michael PLoS Genet Research Article Although most unicellular organisms reproduce asexually, most multicellular eukaryotes are obligately sexual. This implies that there are strong barriers that prevent the origin or maintenance of asexuality arising from an obligately sexual ancestor. By studying rare asexual animal species we can gain a better understanding of the circumstances that facilitate their evolution from a sexual ancestor. Of the known asexual animal species, many originated by hybridization between two ancestral sexual species. The balance hypothesis predicts that genetic incompatibilities between the divergent genomes in hybrids can modify meiosis and facilitate asexual reproduction, but there are few instances where this has been shown. Here we report that hybridizing two sexual Caenorhabditis nematode species (C. nouraguensis females and C. becei males) alters the normal inheritance of the maternal and paternal genomes during the formation of hybrid zygotes. Most offspring of this interspecies cross die during embryogenesis, exhibiting inheritance of a diploid C. nouraguensis maternal genome and incomplete inheritance of C. becei paternal DNA. However, a small fraction of offspring develop into viable adults that can be either fertile or sterile. Fertile offspring are produced asexually by sperm-dependent parthenogenesis (also called gynogenesis or pseudogamy); these progeny inherit a diploid maternal genome but fail to inherit a paternal genome. Sterile offspring are hybrids that inherit both a diploid maternal genome and a haploid paternal genome. Whole-genome sequencing of individual viable worms shows that diploid maternal inheritance in both fertile and sterile offspring results from an altered meiosis in C. nouraguensis oocytes and the inheritance of two randomly selected homologous chromatids. We hypothesize that hybrid incompatibility between C. nouraguensis and C. becei modifies maternal and paternal genome inheritance and indirectly induces gynogenetic reproduction. This system can be used to dissect the molecular mechanisms by which hybrid incompatibilities can facilitate the emergence of asexual reproduction. Public Library of Science 2019-12-16 /pmc/articles/PMC6946170/ /pubmed/31841515 http://dx.doi.org/10.1371/journal.pgen.1008520 Text en © 2019 Lamelza et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lamelza, Piero
Young, Janet M.
Noble, Luke M.
Caro, Lews
Isakharov, Arielle
Palanisamy, Meenakshi
Rockman, Matthew V.
Malik, Harmit S.
Ailion, Michael
Hybridization promotes asexual reproduction in Caenorhabditis nematodes
title Hybridization promotes asexual reproduction in Caenorhabditis nematodes
title_full Hybridization promotes asexual reproduction in Caenorhabditis nematodes
title_fullStr Hybridization promotes asexual reproduction in Caenorhabditis nematodes
title_full_unstemmed Hybridization promotes asexual reproduction in Caenorhabditis nematodes
title_short Hybridization promotes asexual reproduction in Caenorhabditis nematodes
title_sort hybridization promotes asexual reproduction in caenorhabditis nematodes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946170/
https://www.ncbi.nlm.nih.gov/pubmed/31841515
http://dx.doi.org/10.1371/journal.pgen.1008520
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