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. 2021 Jun 16;8(6):202292.
doi: 10.1098/rsos.202292.

No evidence for genetic sex determination in Daphnia magna

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No evidence for genetic sex determination in Daphnia magna

Luca Cornetti et al. R Soc Open Sci. .

Abstract

Mechanisms of sex determination (SD) differ widely across the tree of life. In genotypic sex determination (GSD), genetic elements determine whether individuals are male or female, while in environmental sex determination (ESD), external cues control the sex of the offspring. In cyclical parthenogens, females produce mostly asexual daughters, but environmental stimuli such as crowding, temperature or photoperiod may cause them to produce sons. In aphids, sons are induced by ESD, even though GSD is present, with females carrying two X chromosomes and males only one (X0 SD system). By contrast, although ESD exists in Daphnia, the two sexes were suggested to be genetically identical, based on a 1972 study on Daphnia magna (2n=20) that used three allozyme markers. This study cannot, however, rule out an X0 system, as all three markers may be located on autosomes. Motivated by the life cycle similarities of Daphnia and aphids, and the absence of karyotype information for Daphnia males, we tested for GSD (homomorphic sex chromosomes and X0) systems in D. magna using a whole-genome approach by comparing males and females of three genotypes. Our results confirm the absence of haploid chromosomes or haploid genomic regions in D. magna males as well as the absence of sex-linked genomic regions and sex-specific single-nucleotide polymorphisms. Within the limitations of the three studied populations here and the methods used, we suggest that our results make the possibility of genetic differences among sexes in the widely used Daphnia model system very unlikely.

Keywords: SNPs; X0 sex-determination system; chromosomes; coverage; karyotype; water fleas.

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Figures

Figure 1.
Figure 1.
Violin plots displaying the whole range of coverage ratio female/male values for all the 10 kbp non-overlapping sliding windows considered. Black dots inside the violin plots represent mean, while black whiskers indicate standard deviation. The 10 chromosomes are shown separately, and the three analysed D. magna genotypes are plotted side-by-side (CA: CA-CH-1 from Canada; NO: NO-M3-1 from Norway; RU: RU-KOR1-1 from Russia). Putative sex chromosomes in an X0 sex-determination system should have a coverage ratio close to two, while autosomes have a coverage ratio close to one.

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References

    1. Fusco G, Minelli A. 2019. The biology of reproduction. In Chapter 6: determination of Sex and mating type. Cambridge, UK: Cambridge University Press.
    1. Abbott JK, Nordén AK, Hansson B. 2017. Sex chromosome evolution: Historical insights and future perspectives. Proc. R. Soc. B Biol. Sci. 284, 20162806. (10.1098/rspb.2016.2806) - DOI - PMC - PubMed
    1. Charlesworth B. 1996. The evolution of chromosomal sex determination and dosage compensation. Curr. Biol. 6, 149-162. (10.1016/S0960-9822(02)00448-7) - DOI - PubMed
    1. Bachtrog D, et al. 2014. Sex determination: why so many ways of doing it? PLoS Biol. 12, 1-13. (10.1371/journal.pbio.1001899) - DOI - PMC - PubMed
    1. Hodgkin J. 1987. Primary sex determination in the nematode C. elegans. Development 101, 5-16. - PubMed

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