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Epigenetic mechanisms convey environmental information through generations and can regulate gene expression. Epigenetic studies in wild mammals are rare, but enable understanding adaptation processes as they may occur in nature. In most wild mammal species, males are the dispersing sex and thus often have to cope with differing habitats and thermal changes more rapidly than the often philopatric females. As temperature is a major environmental selection factor, we investigated whether genetically heterogeneous Wild guinea pig (Cavia aperea) males adapt epigenetically to an increase in temperature, whether that response will be transmitted to the next generation(s), and whether it regulates mRNA expression. Five (F0) adult male guinea pigs were exposed to an increased ambient temperature for 2 months, corresponding to the duration of the species' spermatogenesis. To study the effect of heat, we focused on the main thermoregulatory organ, the liver. We analyzed CpG-methylation changes of male offspring (F1) sired before and after the fathers' heat treatment (as has recently been described in Weyrich et al. [Mol. Ecol., 2015]). Transcription analysis was performed for the three genes with the highest number of differentially methylated changes detected: the thermoregulation gene Signal Transducer and Activator of Transcription 3 (Stat3), the proteolytic peptidase gene Cathepsin Z (Ctsz), and Sirtuin 6 (Sirt6) with function in epigenetic regulation. Stat3 gene expression was significantly reduced (P < 0.05), which indicated a close link between CpG-methylation and expression levels for this gene. The two other genes did not show gene expression changes. Our results indicate the presence of a paternal transgenerational epigenetic effect. Quick adaptation to climatic changes may become increasingly relevant for the survival of wildlife species as global temperatures are rising.
Reciprocal selection between aphids, their protective endosymbionts, and the parasitoid wasps that prey upon them offers an opportunity to study the basis of their coevolution. We investigated adaptation to symbiont‐conferred defense by rearing the parasitoid wasp Lysiphlebus fabarum on aphids (Aphis fabae) possessing different defensive symbiont strains (Hamiltonella defensa). After ten generations of experimental evolution, wasps showed increased abilities to parasitize aphids possessing the H. defensa strain they evolved with, but not aphids possessing the other strain. We show that the two symbiont strains encode different toxins, potentially creating different targets for counter‐adaptation. Phenotypic and behavioral comparisons suggest that neither life‐history traits nor oviposition behavior differed among evolved parasitoid lineages. In contrast, comparative transcriptomics of adult female wasps identified a suite of differentially expressed genes among lineages, even when reared in a common, symbiont‐free, aphid host. In concurrence with the specificity of each parasitoid lineages’ infectivity, most differentially expressed parasitoid transcripts were also lineage‐specific. These transcripts are enriched with putative venom toxins and contain highly expressed, potentially defensive viral particles. Together, these results suggest that wild populations of L. fabarum employ a complicated offensive arsenal with sufficient genetic variation for wasps to adapt rapidly and specifically to their hosts’ microbial defenses.
Sphagnum magellanicum Brid. is a worldwide distributed peat moss and an ecosystem-engineer in temperate and boreal bog ecosystems suggesting a great adaptive potential to different environmental conditions. Phenotypes of S. magellanicum have been described as one species so far, although this has been questioned by the detection of several genetic groups in a recent global study. Concordant with morphological uniformity, our analyses of Mid-to Northern European plants revealed only minimal variation in nuclear nrITS and plastid rps4 sequences. However, we detected two distinct genetic groups within Europe by analyzing microsatellite data of 298 individuals from 27 populations. Plants formed an Eastern and a Western European cluster, with overlapping areas in northern Germany and southern Sweden where plants of both clusters coexist within populations but show no signs of admixture. These two cryptic taxa seem therefore to be reproductively isolated. Bayesian analyses indicated that reproductive isolation occurred before the end of the late Pleistocene glaciations. After the meltdown of the glaciers, both clusters colonized northern and central Europe from glacial refugia in the West and possibly from Euro-Siberian populations. To test for divergent adaptation to environmental conditions, we exposed plants of both clusters to experimental climate warming treatments at two different plant-diversity levels (monocultures vs. mixtures) for two years. Despite their different evolutionary history, plants of both genetic clusters responded equally to climate treatments in our southern common garden near Potsdam, Germany. However, only eastern cluster populations benefited from plant-community diversity and increased their biomass in mixtures. These differences in their ecological niche match the diverging microhabitat preferences observed in situ and may effectively hamper genetic exchange if distances between microhabitats are too large for Sphagnum sperm movement. (C) 2017 Elsevier GmbH. All rights reserved.