Yerba mate (Ilex paraguariensis) genome provides new insights into convergent evolution of caffeine biosynthesis

Author:

Vignale Federico A.ORCID,Garcia Andrea Hernandez,Modenutti Carlos P.ORCID,Sosa Ezequiel J.,Defelipe Lucas A.ORCID,Oliveira Renato R.M.ORCID,Nunes Gisele L.ORCID,Acevedo Raúl M.ORCID,Burguener German F.,Rossi MaximilianoORCID,Zapata Pedro D.ORCID,Marti Dardo A.ORCID,Oliveira GuilhermeORCID,Smith Madeline N.,Dubs Nicole M.,Nair Satish,Barkman Todd J.,Turjanski Adrian G.ORCID

Abstract

AbstractYerba mate (Ilex paraguariensis) is an economically important crop marketed for the elaboration of mate, the third-most widely consumed caffeine-containing infusion worldwide. Here we report the first genome assembly of this species, which has a total length of 1.06 Gb and contains 53,390 protein-coding genes. Comparative analyses revealed that the large yerba mate genome size is partly due to a whole-genome duplication (Ip-α) during the early evolutionary history ofIlex, in addition to the hexaploidization event (γ) shared by core eudicots. Characterization of the genome allowed us to clone the genes encoding methyltransferase enzymes that catalyse multiple reactions required for caffeine production. To our surprise, this species has converged upon a different biochemical pathway compared to that of its relatives, coffee and tea. In order to gain insight into the structural basis for the convergent enzyme activities, we obtained a crystal structure for the terminal enzyme in the pathway that forms caffeine. The structure reveals that convergent solutions have evolved for substrate positioning because different amino acid residues facilitate a different substrate orientation such that efficient methylation occurs in the independently evolved enzymes in yerba mate and coffee. While our results show phylogenomic constraint limits the genes coopted for convergence of caffeine biosynthesis, the x-ray diffraction data suggests structural constraints are minimal for the convergent evolution of individual reactions.

Publisher

Cold Spring Harbor Laboratory

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