Genome‐guided investigation of plant natural product biosynthesis. (11th April 2015)

• Record Type: Journal Article
• Authors: Kellner, Franziska; Kim, Jeongwoon; Clavijo, Bernardo J.; Hamilton, John P.; Childs, Kevin L.; Vaillancourt, Brieanne; Cepela, Jason; Habermann, Marc; Steuernagel, Burkhard; Clissold, Leah; McLay, Kirsten; Buell, Carol Robin; O'Connor, Sarah E.
• Is Part Of: Plant journal. Volume 82:Number 4(2015:May)
• Page Start: 680
• Page End: 692
• Publication Date: 2015-04-11
• Subjects: Plant molecular biology -- Periodicals; Plant cells and tissues -- Periodicals; Botany -- Periodicals; 580
• DOI: 10.1111/tpj.12827
• Languages: English
• ISSNs: 0960-7412

Abstract

<abstract abstract-type="main" id="tpj12827-abs-0001"> <title>Summary</title> <p>The medicinal plant Madagascar periwinkle, <italic>Catharanthus roseus</italic> (L.) G. Don, produces hundreds of biologically active monoterpene‐derived indole alkaloid (MIA) metabolites and is the sole source of the potent, expensive anti‐cancer compounds vinblastine and vincristine. Access to a genome sequence would enable insights into the biochemistry, control, and evolution of genes responsible for MIA biosynthesis. However, generation of a near‐complete, scaffolded genome is prohibitive to small research communities due to the expense, time, and expertise required. In this study, we generated a genome assembly for <italic>C. roseus</italic> that provides a near‐comprehensive representation of the genic space that revealed the genomic context of key points within the MIA biosynthetic pathway including physically clustered genes, tandem gene duplication, expression sub‐functionalization, and putative neo‐functionalization. The genome sequence also facilitated high resolution co‐expression analyses that revealed three distinct clusters of co‐expression within the components of the MIA pathway. Coordinated biosynthesis of precursors and intermediates throughout the pathway appear to be a feature of vinblastine/vincristine biosynthesis. The <italic>C. roseus</italic> genome also revealed localization of enzyme‐rich genic regions and transporters near known biosynthetic enzymes, highlighting how even a draft genome sequence can empower the study of high‐value specialized metabolites.</p> </abstract>