The Vinca minor genome highlights conserved evolutionary traits in monoterpene indole alkaloid synthesis

Author:

Stander Emily Amor1ORCID,Cuello Clément1ORCID,Birer-Williams Caroline1,Kulagina Natalja1ORCID,Jansen Hans J2ORCID,Carqueijeiro Ines1ORCID,Méteignier Louis-Valentin1ORCID,Vergès Valentin1,Oudin Audrey1ORCID,Papon Nicolas3ORCID,Dirks Ron P2ORCID,Jensen Michael Krogh4ORCID,O’Connor Sarah Ellen5ORCID,Dugé de Bernonville Thomas1ORCID,Besseau Sébastien1ORCID,Courdavault Vincent1ORCID

Affiliation:

1. Biomolécules et Biotechnologies Végétales, EA2106, Université de Tours , 37200 Tours, France

2. Future Genomics Technologies , 2333 BE Leiden, The Netherlands

3. Univ Angers, Univ Brest, IRF, SFR ICAT , F-49000 Angers, France

4. Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark , 2800 Kongens Lyngby, Denmark

5. Department of Natural Product Biosynthesis, Max Planck Institute for Chemical Ecology , Jena 07745, Germany

Abstract

Abstract Vinca minor, also known as the lesser periwinkle, is a well-known species from the Apocynaceae, native to central and southern Europe. This plant synthesizes monoterpene indole alkaloids, which are a class of specialized metabolites displaying a wide range of bioactive- and pharmacologically important properties. Within the almost 50 monoterpene indole alkaloids it produces, V. minor mainly accumulates vincamine, which is commercially used as a nootropic. Using a combination of Oxford Nanopore Technologies long read- and Illumina short-read sequencing, a 679,098 Mb V. minor genome was assembled into 296 scaffolds with an N50 scaffold length of 6 Mb, and encoding 29,624 genes. These genes were functionally annotated and used in a comparative genomic analysis to establish gene families and to investigate gene family expansion and contraction across the phylogenetic tree. Furthermore, homology-based monoterpene indole alkaloid gene predictions together with a metabolic analysis across 4 different V. minor tissue types guided the identification of candidate monoterpene indole alkaloid genes. These candidates were finally used to identify monoterpene indole alkaloid gene clusters, which combined with synteny analysis allowed for the discovery of a functionally validated vincadifformine-16-hydroxylase, reinforcing the potential of this dataset for monoterpene indole alkaloids gene discovery. It is expected that access to these resources will facilitate the elucidation of unknown monoterpene indole alkaloid biosynthetic routes with the potential of transferring these pathways to heterologous expression systems for large-scale monoterpene indole alkaloid production.

Funder

EU Horizon 2020 research and innovation program

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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