Genetic Evidence for Sexuality in Cochliopodium (Amoebozoa).

J Hered

Department of Biology, Spelman College, 350 Spelman Lane Southwest, Atlanta, GA 30314.

Published: October 2017

AI Article Synopsis

  • - Microbial eukaryotes like amoeboids have complex life cycles that may involve sexual reproduction, with recent studies suggesting that the Amoebozoa group is ancestrally sexual; however, some have very low detection of sex-related genes.
  • - In the genus Cochliopodium, known for its unique processes of cell fusion and karyogamy, previous findings showed no meiosis genes; this study generates extensive transcriptome data to better understand its genetic basis and lifecycle.
  • - The study identified a higher number of sex-related genes, including previously undetected meiosis genes, revealing that Cochliopodium has the genetic tools for sexual recombination, although the specifics of its fusion and genome reduction mechanisms are still

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892394PMC
http://dx.doi.org/10.1093/jhered/esx078DOI Listing

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