Retention and loss of amino acid biosynthetic pathways based on analysis of whole-genome sequences

Abstract

Plants and fungi can synthesize each of the 20 amino acids by using biosynthetic pathways inherited from their bacterial ancestors. However, the ability to synthesize nine amino acids (Phe, Trp, Ile, Leu, Val, Lys, His, Thr, and Met) was lost in a wide variety of eukaryotes that evolved the ability to feed on other organisms. Since the biosynthetic pathways and their respective enzymes are well characterized, orthologs can be recognized in whole genomes to understand when in evolution pathways were lost. The pattern of pathway loss and retention was analyzed in the complete genomes of three early-diverging protist parasites, the amoeba Dictyostelium, and six animals. The nine pathways were lost independently in animals, Dictyostelium, Leishmania, Plasmodium, and Cryptosporidium. Seven additional pathways appear to have been lost in one or another parasite, demonstrating that they are dispensable in a nutrition-rich environment. Our predictions of pathways retained and pathways lost based on computational analyses of whole genomes are validated by minimal-medium studies with mammals, fish, worms, and Dictyostelium. The apparent selective advantages of retaining biosynthetic capabilities for amino acids available in the diet are considered.

FIG. 1.

Evolutionary tree depicting the branching order of the organisms studied (adapted from reference 15). The tree is rooted on seven archaebacterial genomes. Abbreviations: Ch, C. hominis; Pf, P. falciparum; At, A. thaliana; Dd, D. discoideum; Sc, S. cerevisiae; Hs, H. sapiens; Tn, T. nigroviridis; Ci, C. intestinalis; Ag, A. gambiae; Dm, D. melanogaster; Ce, C. elegans; Lm, L. major.