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Hofmann, G. E.

Publications and source records attributed to Hofmann, G. E..

2 recordsLinked to original sources

Transgenerational effects alter the fitness consequences and genetic architecture of phenotypic plasticity and its regulatory pathways

Transgenerational effects, where parental environments influence offspring phenotype, facilitate acclimation over ecological timescales. Transgenerational effects may also influence evolution by altering the fitness costs of offspring traits and the expression of genetic variation. We tested the evolutionary role of transgenerational effects in the sea urchin Strongylocentrotus purpuratus, whose populations are exposed to coastal upwelling (periods of low temperature and pH) and exhibit local adaptation, parental effects, and phenotypic plasticity in response to upwelling. Using a quantitative genetic breeding design, we conditioned parents and larvae to upwelling or control conditions and combined RNA-seq with larval phenotyping (body size, biomineralization, survival). Larval upwelling exposure caused widespread differential expression (DE), reduced biomineralization, and reduced size. Survival was linked to biomineralization, body size, and their plasticity under upwelling, but only in offspring of upwelling-conditioned parents -evidence that parental environment affected selection on offspring traits. DE under upwelling was associated with adaptive plasticity in biomineralization and size, but adaptive gene expression changes shared negative genetic correlations. However, genetic correlations in gene expression associated with body size plasticity were significantly more positive in larvae from upwelling parents. Parental conditioning strengthened selection on offspring performance and reduced genetic tradeoffs between performance-associated expression pathways, potentially accelerating adaptation.

evolutionary biology↗

Gene regulation by DNA methylation is contingent on chromatin accessibility during transgenerational plasticity in the purple sea urchin

Epigenetic processes are proposed to contribute to phenotypic plasticity. In invertebrates, DNA methylation commonly varies across environments and can correlate or causally associate with phenotype, but its role in transcriptional responses to the environment remains unclear. Maternal environments experienced by the sea urchin Strongylocentrotus purpuratus induce 3 - 6x greater differential CpG methylation in offspring larvae relative to larval developmental environments, suggesting a role for DNA methylation in transgenerational plasticity (TGP). However, a negligible association has been observed between differentially methylated and differentially expressed genes. What gene regulatory roles does invertebrate DNA methylation possess under environmental change, if any? We quantified DNA methylation and gene expression in S. purpuratus larvae exposed to different ecologically relevant conditions during gametogenesis (maternal conditioning) or embryogenesis (developmental conditioning). We modeled differential gene expression and differential splicing under maternal conditioning as functions of DNA methylation, incorporating variables for genomic feature and chromatin accessibility. We detected significant interactions between differential methylation, chromatin accessibility, and genic architecture associated with differential expression and splicing. Observed transcriptional responses to maternal conditioning were also 4 - 13x more likely when accounting for interactions between methylation and chromatin accessibility. Our results provide evidence that DNA methylation possesses multiple functional roles during TGP in S. purpuratus, but its effects are contingent upon other genomic and epigenomic states. Singularly unpredictive of transcription, DNA methylation is likely one cog in the epigenomic machinery contributing to environmental responses and phenotypic plasticity in S. purpuratus and other invertebrates.

genomics↗