Until recently, the impact of HGT on eukaryotic evolution was thought to be limited (Kurland et al., 2003). The reasons for this viewpoint included limited eukaryotic genomic data, perceived problems associated with overcoming germ

and soma separation in multicellular organisms and the apparent inhibition of large-scale searches for HGT following high-profile erroneous reports of prokaryotic genes in the human genome (Lander et al., 2001; Stanhope et al., 2001). The rapid increase in publicly available eukaryotic genomic data has changed our views on the frequency and learn more subsequent important roles HGT may play in eukaryotic evolution (especially unicellular organisms). For example, the transfer of a number of prokaryotic genes into the amoeba Entamoeba histolytica has altered its metabolic capabilities increasing its range of substrates to include tryptophanase and aspartase (Loftus et al., 2005). Similarly, prokaryote genes transferred into the social amoebae Dictyostelium discoideum give it the ability to degrade bacterial cell walls (dipeptidase), resist the toxic effects of tellurite (terD) and scavenge iron (siderophore; Eichinger et al., 2005). The presence of bacterial genes in phagotrophic eukaryotes was initially explained

by the ‘you are what you eat hypothesis’ (Doolittle, 1998). However, the presence of bacterial genes in nonphagotrophic organisms (including members of Selleckchem AG14699 the fungal kingdom) has shown that mechanisms other than phagocytosis are responsible. Because of their roles as human/crop

pathogens, relative small genome size and importance in the field of biotechnology, over 100 fungal species have been fully sequenced to date. This abundance of fungal data permits us to investigate the frequency and possible consequences HGT has played in fungal evolution. This review sets out to describe the methodology commonly used to locate HGT, the consequences it has played in fungal evolution and possible concerns for reconstructing the fungal tree of life (FTOL). Several approaches can be taken to detect incidences of HGT. These include patchy phyletic distribution of a gene (Fitzpatrick et al., 2008; Fig. 1a), locating shared introns in the genes of unrelated species indicating PRKACG monophyly (Kondrashov et al., 2006), alternatively locating intronless genes in a species that is generally intron rich could indicate an acquisition from a bacterial source (Garcia-Vallve et al., 2000; Schmitt & Lumbsch, 2009), also finding similar genes shared amongst unrelated species that share a specific niche/geographical location (Kunin et al., 2005) or locating genes with conserved synteny blocks that are present in two or more species but absent from close relatives (Fitzpatrick et al., 2008; Rolland et al., 2009; Fig. 1b). However, the most convincing method to detect HGT uses phylogenetic inference (Ragan, 2001; Fig. 1c).