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Comparative transcriptomic analysis provides novel insights into mescaline biosynthesis by Lophophora williamsii.

Eun-Mi Hwang, Kyu-Sik Jeong, Seong Yeon Yoo, Jihyun Kim, Sanggil Choe, Joo-Young Kim

Journal of forensic sciences March 1, 2025 DOI: 10.1111/1556-4029.15679 via PubMed

Summary

AI-generated from the abstract

A full-length transcriptome of Lophophora williamsii (peyote) was generated using single-molecule real-time PCR and PacBio Iso-Seq, yielding 2,839,819 base pairs of long reads and 70,945 unigenes. Known genes in the mescaline biosynthetic pathway were confirmed, including 6 tyrosine decarboxylases, 1 tyrosine/DOPA decarboxylase, 215 O-methyltransferases, and 129 hydroxylases. Gene Ontology analysis identified 2903 biological processes, 695 cellular components, and 1766 molecular functions. KEGG pathway analysis linked phenylpropanoid and isoquinoline biosynthesis to mescaline production. Illumina Nova sequencing compared gene expression between mescaline-positive and mescaline-negative specimens to establish a candidate gene pool. The findings call for re-evaluation of forensic methods and legal regulations for newly identified L. williamsii specimens.

Study at a glance

Characteristics Transcriptome sequencing and gene expression comparison Peer reviewed
Population Lophophora williamsii specimens (mescaline-positive and mescaline-negative)
Topics Mescaline
Keywords Lophophora williamsii Iso‐sequencing Transcriptome sequencing
Key finding A full-length transcriptome of L. williamsii was generated, confirming genes in the mescaline biosynthetic pathway and identifying candidate genes that differ between mescaline-positive and mescaline-negative specimens.

Abstract

Lophophora williamsii, known for mescaline synthesis, has raised legal and ethical considerations. However, L. williamsii specimens that do not contain mescaline have been recently identified, necessitating the development of techniques to differentiate between mescaline-positive and mescaline-negative groups. Genetic markers have been explored to differentiate these specimens, complementing gas chromatography/mass spectrometry analysis. Here, we used a single-molecule real-time polymerase chain reaction to generate a full-length L. williamsii transcriptome and elucidate the mechanisms underlying mescaline biosynthesis. In total, 2,839,819 base pairs of highly accurate long reads were obtained using PacBio Iso-Seq and 70,945 unigenes were obtained through transcriptome sequencing. Known genes involved in the mescaline biosynthetic pathway were confirmed in the L. williamsii transcriptome, including 6 genes encoding tyrosine decarboxylases, 1 encoding tyrosine/DOPA decarboxylase, 215 encoding O-methyltransferases, and 129 encoding hydroxylases. Gene Ontology analysis revealed 2903 biological processes, 695 cellular components, and 1766 molecular functions. The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed two biosynthetic pathways, namely, phenylpropanoid and isoquinoline biosynthesis, associated with mescaline biosynthesis. To investigate genetic differences based on the presence of mescaline, Illumina Nova sequencing was conducted. The expression levels of genes involved in mescaline biosynthesis were compared to establish a candidate gene pool based on the presence of mescaline. Subsequently, functional annotation was performed on the identified candidate genes using a genetic database derived from PacBio sequencing. These findings underscore the need for a re-evaluation of forensic methods and legal regulations concerning newly identified L. williamsii specimens.

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