Ancestral sequence reconstruction (ASR) is typically performed using homogeneous evolutionary models, which assume that the same substitution propensities affect all sites and lineages. These assumptions are routinely violated: heterogeneous structural and functional constraints favor different amino acid states at different sites, and these constraints often change among lineages as epistatic substitutions accrue at other sites. To evaluate how realistic violations of the homogeneity assumption affect ASR, we developed site-specific substitution models and parameterized them using data from deep mutational scanning experiments on three protein families; we then used these models to perform ASR on the empirical alignments and on alignments simulated under heterogeneous conditions derived from the experiments.
View Article and Find Full Text PDFPathogen specialization may not always arise due to an adaptive trade-off between infecting one or many species. Bruns et al. characterized the potential host range of four lineages of the fungal pathogen Microbotryum on three Dianthus species.
View Article and Find Full Text PDF