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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2017
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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. |
format | Online Article Text |
id | pubmed-5892394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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