Back

Convergent evolution of plant prickles is drivenby repeated gene co-option over deep time

Satterlee, J. W.; Alonso, D.; Gramazio, P.; Jenike, K. M.; He, J.; Arrones, A.; Villanueva, G.; Plazas, M.; Ramakrishnan, S.; Benoit, M.; Gentile, I.; Hendelman, A.; Shohat, H.; Fitzgerald, B.; Robitaille, G. M.; Green, Y.; Swartwood, K.; Passalacqua, M. J.; Gagnon, E.; Hilgenhof, R.; Huggins, T. D.; Eizenga, G. C.; Gur, A.; Rutten, T.; Stein, N.; Yao, S.; Bellot, C.; Bendahmane, M.; Frary, A.; Knapp, S.; Sarkinen, T.; Gillis, J.; Van Eck, J.; Schatz, M. C.; Eshed, Y.; Prohens, J.; Vilanova, S.; Lippman, Z. B.

2024-02-22 evolutionary biology
10.1101/2024.02.21.581474 bioRxiv
Show abstract

An enduring question in evolutionary biology concerns the degree to which episodes of convergent trait evolution depend on the same genetic programs, particularly over long timescales. Here we genetically dissected repeated origins and losses of prickles, sharp epidermal projections, that convergently evolved in numerous plant lineages. Mutations in a cytokinin hormone biosynthetic gene caused at least 16 independent losses of prickles in eggplants and wild relatives in the genus Solanum. Strikingly, homologs promote prickle formation across angiosperms that collectively diverged over 150 million years ago. By developing new Solanum genetic systems, we leveraged this discovery to eliminate prickles in a wild species and an indigenously foraged berry. Our findings implicate a shared hormone-activation genetic program underlying evolutionarily widespread and recurrent instances of plant morphological innovation.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.