Abstract

DNA methylation is an important epigenetic modification that has been repeatedly implied in organismal adaptation. However, many previous studies that have linked DNA methylation patterns to environmental parameters have been limited by confounding factors, such as cell-type heterogeneity and genetic variation. In this study, we analyzed DNA methylation variation in marbled crayfish, a clonal and invasive freshwater crayfish that is characterized by a largely tissue-invariant methylome and negligible genetic variation. Using a capture-based subgenome bisulfite sequencing approach that covers a small, variably methylated portion of the marbled crayfish genome, we identified specific and highly localized DNA methylation signatures for specimens from geographically and ecologically distinct wild populations. These results were replicated both biologically and technically by re-sampling at different time points and by using independent methodology. Finally, we show specific methylation signatures for laboratory animals and for laboratory animals that were reared at a lower temperature. Our results thus demonstrate the existence of context-dependent DNA methylation signatures in a clonal animal.

Highlights

  • DNA methylation is a highly conserved epigenetic modification (Law and Jacobsen, 2010; Schubeler, 2015)

  • We have previously shown that DNA methylation in the marbled crayfish is targeted to gene bodies, and that DNA methylation patterns are largely stable and tissue-invariant (Gatzmann et al, 2018)

  • Tissue-specific methylation differences were highly stable between the two populations (Figures 4B,C). These findings suggest the existence of localized tissue-specific methylation patterns in marbled crayfish

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Summary

Introduction

DNA methylation is a highly conserved epigenetic modification (Law and Jacobsen, 2010; Schubeler, 2015). Animal DNA methylation is found mainly in the CpG sequence context, with major differences in methylation patterning between species (Breiling and Lyko, 2015; Schubeler, 2015). It has been hypothesized that an important function of DNA methylation is to adapt genomes to changing environments (Jaenisch and Bird, 2003; Feil and Fraga, 2012). Pioneering work in this context has been performed in Arabidopsis thaliana, a globally distributed plant that is characterized by locally adapted phenotypes (Atwell et al, 2010). Later comparisons of genetic and epigenetic variances explained most of the methylation changes by genetic polymorphisms (Dubin et al, 2015), which are frequent in this species and define the large number of genetic ecotypes, rather than epigenetic ecotypes (Ferrero-Serrano and Assmann, 2019)

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