TY - JOUR T1 - Convergent evolution of psilocybin biosynthesis by psychedelic mushrooms JF - bioRxiv DO - 10.1101/374199 SP - 374199 AU - Ali R. Awan AU - Jaclyn M. Winter AU - Daniel Turner AU - William M. Shaw AU - Laura M. Suz AU - Alexander J. Bradshaw AU - Tom Ellis AU - Bryn T.M. Dentinger Y1 - 2018/01/01 UR - http://biorxiv.org/content/early/2018/07/25/374199.abstract N2 - Psilocybin is a psychoactive compound with clinical applications produced by dozens of mushroom species1. There has been a longstanding interest in psilocybin research with regard to treatment for addiction2, depression3, and end-of-life suffering4. However, until recently very little was known about psilocybin biosynthesis and its ecological role. Here we confirm and refine recent findings5 about the genes underpinning psilocybin biosynthesis, discover that there is more than one psilocybin biosynthesis cluster in mushrooms, and we provide the first data directly addressing psilocybin’s ecological role. By analysing independent genome assemblies for the hallucinogenic mushrooms Psilocybe cyanescens and Pluteus salicinus we recapture the recently discovered psilocybin biosynthesis cluster5,6 and show that a transcription factor previously implicated in its regulation is actually not part of the cluster. Further, we show that the mushroom Inocybe corydalina produces psilocybin but does not contain the established biosynthetic cluster, and we present an alternative cluster. Finally, a meta-transcriptome analysis of wild-collected mushrooms provides evidence for intra-mushroom insect gene expression of flies whose larvae grow inside Psilocybe cyanescens. These larvae were successfully reared into adults. Our results show that psilocybin does not confer complete protection against insect mycophagy, and the hypothesis that it is produced as an adaptive defense compound may need to be reconsidered. ER -