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Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)

Microbial eukaryotes, including amoeboids, display diverse and complex life cycles that may or may not involve sexual reproduction. A recent comprehensive gene inventory study concluded that the Amoebozoa are ancestrally sexual. However, the detection of sex genes in some lineages known for their po...

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Autores principales: Wood, Fiona C, Heidari, Alireza, Tekle, Yonas I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892394/
https://www.ncbi.nlm.nih.gov/pubmed/29036297
http://dx.doi.org/10.1093/jhered/esx078
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author Wood, Fiona C
Heidari, Alireza
Tekle, Yonas I
author_facet Wood, Fiona C
Heidari, Alireza
Tekle, Yonas I
author_sort Wood, Fiona C
collection PubMed
description Microbial eukaryotes, including amoeboids, display diverse and complex life cycles that may or may not involve sexual reproduction. A recent comprehensive gene inventory study concluded that the Amoebozoa are ancestrally sexual. However, the detection of sex genes in some lineages known for their potentially sexual life cycle was very low. Particularly, the genus Cochliopodium, known to undergo a process of cell fusion, karyogamy, and subsequent fission previously described as parasexual, had no meiosis genes detected. This is likely due to low data representation, given the extensive nuclear fusion observed in the genus. In this study, we generate large amounts of transcriptome data for 2 species of Cochliopodium, known for their high frequency of cellular and nuclear fusion, in order to study the genetic basis of the complex life cycle observed in the genus. We inventory 60 sex-related genes, including 11 meiosis-specific genes, and 31 genes involved in fusion and karyogamy. We find a much higher detection of sex-related genes, including 5 meiosis-specific genes not previously detected in Cochliopodium, in this large transcriptome data. The expressed genes form a near-complete recombination machinery, indicating that Cochliopodium is an actively recombining sexual lineage. We also find 9 fusion-related genes in Cochliopodium, although no conserved fusion-specific genes were detected in the transcriptomes. Cochliopodium thus likely uses lineage specific genes for the fusion and depolyploidization processes. Our results demonstrate that Cochliopodium possess the genetic toolkit for recombination, while the mechanism involving fusion and genome reduction remains to be elucidated.
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spelling pubmed-58923942018-04-13 Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa) Wood, Fiona C Heidari, Alireza Tekle, Yonas I J Hered Symposium Articles Microbial eukaryotes, including amoeboids, display diverse and complex life cycles that may or may not involve sexual reproduction. A recent comprehensive gene inventory study concluded that the Amoebozoa are ancestrally sexual. However, the detection of sex genes in some lineages known for their potentially sexual life cycle was very low. Particularly, the genus Cochliopodium, known to undergo a process of cell fusion, karyogamy, and subsequent fission previously described as parasexual, had no meiosis genes detected. This is likely due to low data representation, given the extensive nuclear fusion observed in the genus. In this study, we generate large amounts of transcriptome data for 2 species of Cochliopodium, known for their high frequency of cellular and nuclear fusion, in order to study the genetic basis of the complex life cycle observed in the genus. We inventory 60 sex-related genes, including 11 meiosis-specific genes, and 31 genes involved in fusion and karyogamy. We find a much higher detection of sex-related genes, including 5 meiosis-specific genes not previously detected in Cochliopodium, in this large transcriptome data. The expressed genes form a near-complete recombination machinery, indicating that Cochliopodium is an actively recombining sexual lineage. We also find 9 fusion-related genes in Cochliopodium, although no conserved fusion-specific genes were detected in the transcriptomes. Cochliopodium thus likely uses lineage specific genes for the fusion and depolyploidization processes. Our results demonstrate that Cochliopodium possess the genetic toolkit for recombination, while the mechanism involving fusion and genome reduction remains to be elucidated. Oxford University Press 2017-10 2017-09-27 /pmc/articles/PMC5892394/ /pubmed/29036297 http://dx.doi.org/10.1093/jhered/esx078 Text en © The American Genetic Association 2017. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Symposium Articles
Wood, Fiona C
Heidari, Alireza
Tekle, Yonas I
Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)
title Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)
title_full Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)
title_fullStr Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)
title_full_unstemmed Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)
title_short Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa)
title_sort genetic evidence for sexuality in cochliopodium (amoebozoa)
topic Symposium Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892394/
https://www.ncbi.nlm.nih.gov/pubmed/29036297
http://dx.doi.org/10.1093/jhered/esx078
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