Phylogenomics: Constructing Species Phylogenies from Multi-Locus Data

Introduction One of the fascinating challenges in estimating the evolutionary history of a set of species is that different regions within the genomes can evolve differently due to various biological phenomena (Maddison, 1997; Mallo and Posada, 2016; Posada, 2016). One of the most obvious causes for this difference is horizontal gene transfer (Syvanen, 1985), whereby DNA is transferred from the genome of one species into that of another. Horizontal gene transfer (HGT) is especially frequent among prokaryotes (Gogarten et al., 2002), but occurs in other organisms as well. While it can be argued that a species tree is useful as a model (Mindell, 2013) and can make sense in the presence of HGT (even for prokaryotes) if it is based on genes that are resistant to HGT, a full depiction of evolutionary history when HGT has occurred requires a more general graphical model called a “phylogenetic network” (Morrison, 2014a). Hybrid speciation, where two different species have viable offspring, is another biological process that requires a phylogenetic network. Well-known examples of hybridization include mules and hinnies (which are hybrids of horses and donkeys) and ligers and tigons (which are the hybrid offspring of lions and tigers). Hybrid speciation has long been known to be common in plants (Rieseberg, 1997), and its extent in other organisms is increasingly apparent (Pennisi, 2016). Like HGT, a proper representation of the evolutionary history of a dataset in which hybridization appears requires a phylogenetic network, rather than a tree. There are also biological processes that cause different parts of the genomes to evolve differently, but where the species history is still correctly modeled as a tree. For example, under a gene duplication and loss model (Ohno, 1970), a gene evolves within the branches of a species tree with duplication events (that increase the number of copies of the gene within a lineage) and loss events (that reduce the number of copies of a gene), so that a given species can have multiple copies of the same gene within its genome. Another process that can create discordance with the species tree is the multi-species coalescent (MSC) model (Maddison, 1997; Pamilo and Nei, 1998) (i.e., the multi-species version of the coalescent process), which models how alleles segregate into populations, and so reflects population-level processes.