De novo genome assembly of Camptotheca acuminata, a natural source of the anti-cancer compound camptothecin. Issue 9 (24th July 2017)

• Record Type: Journal Article
• Authors: Zhao, Dongyan; Hamilton, John P.; Pham, Gina M.; Crisovan, Emily; Wiegert-Rininger, Krystle; Vaillancourt, Brieanne; DellaPenna, Dean; Buell, C. Robin
• Is Part Of: GigaScience. Volume 6:Issue 9(2017)
• Publication Date: 2017-07-24
• Subjects: Camptotheca acuminata -- camptothecin -- genome assembly -- genome annotation -- tandem duplications; Information storage and retrieval systems -- Research -- Periodicals; Biology -- Research -- Periodicals; Medical sciences -- Research -- Periodicals; Database management -- Periodicals; 570.285
• DOI: 10.1093/gigascience/gix065
• Languages: English
• ISSNs: 2047-217X

Abstract

Abstract: Camptotheca acuminata is 1 of a limited number of species that produce camptothecin, a pentacyclic quinoline alkaloid with anti-cancer activity due to its ability to inhibit DNA topoisomerase. While transcriptome studies have been performed previously with various camptothecin-producing species, no genome sequence for a camptothecin-producing species is available to date. We generated a high-quality de novo genome assembly for C. acuminata representing 403 174 860 bp on 1394 scaffolds with an N50 scaffold size of 1752 kbp. Quality assessments of the assembly revealed robust representation of the genome sequence including genic regions. Using a novel genome annotation method, we annotated 31 825 genes encoding 40 332 gene models. Based on sequence identity and orthology with validated genes from Catharanthus roseus as well as Pfam searches, we identified candidate orthologs for genes potentially involved in camptothecin biosynthesis. Extensive gene duplication including tandem duplication was widespread in the C. acuminata genome, with 2571 genes belonging to 997 tandem duplicated gene clusters. To our knowledge, this is the first genome sequence for a camptothecin-producing species, and access to the C. acuminata genome will permit not only discovery of genes encoding the camptothecin biosynthetic pathway but also reagents that can be used for heterologous expression of camptothecin and camptothecin analogs with novel pharmaceutical applications.