Yelle Vandenboer, Koen Martens, Francesc Mesquita-Joanes, and Isa Schön (2024)
Environmental factors and UV exposure affect gene activity in the putative ancient asexual ostracod Darwinula stevensoni
10th European Ostracodologists' Meeting (EOM10).
The non-marine ostracod Darwinula stevensoni (Ostracoda, Crustaceae) is one of the last remaining examples of an ancient asexual (Schön et al. 2009) and has probably abandoned sexual reproduction approximately 20 million years ago (Straub 1952). In spite of the limited genetic diversity of D. stevensoni, its cosmopolitan distribution in different aquatic habitats indicate that this species can survive asexually in the long-term, possibly because it developed a general purpose genotype (Van Doninck et al. 2002). To unravel the genetic background of this general purpose genotype, we have studied gene activity of D. stevensoni via the RNA sequencing of transcriptomes. The transcriptome is the collection of all active genes which have been transcribed from DNA to RNA under certain conditions. Statistically comparing the genetic composition of transcriptomes allows us to identify differences in active (or expressed) genes, which inform on host adaptations to specific conditions. We characterised transcriptomes of D. stevensoni from natural populations in Spain, England and Belgium. To summarize results in our multi-gene approach, the “gene ontology” (GO) classification system was used which divides genes across groups (“terms”) in accordance to the biological function, molecular pathway or cellular component they affect. Of the 5013 terms which were assessed regarding biological function, 49 were found to have significantly different gene expression between the three different populations. However, none of these terms could be directly linked to temperature-related functions, suggesting that differences in gene expression between natural D. stevensoni populations are more complex and do not only reflect adaptation to varying temperature ranges. Living D. stevensoni individuals from the Belgian population were also exposed to UV-radiation in the lab. In this experiment, we expected to find an increased activity of genes being related to the repair and preservation of DNA countering the effects of UV-radiation. Of the same 5013 analysed gene terms, only 9 showed a significant change in
gene expression in response to UV-radiation. None of these gene term had known repair functions, potentially highlighting again more complex gene expression patterns in D. stevensoni than initially expected. More analyses are currently ongoing to unravel the functionality of the activated genes in more detail. We are also planning an experimental set up to directly study gene expression differences of D. stevensoni under different temperatures.
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