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Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides

Calotropis gigantea produces specialized secondary metabolites known as cardenolides, which have anticancer and antimalarial properties. Although transcriptomic studies have been conducted in other cardenolide-producing species, no nuclear genome assembly for an Asterid cardenolide-producing species...

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Autores principales: Hoopes, Genevieve M., Hamilton, John P., Kim, Jeongwoon, Zhao, Dongyan, Wiegert-Rininger, Krystle, Crisovan, Emily, Buell, C. Robin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919723/
https://www.ncbi.nlm.nih.gov/pubmed/29237703
http://dx.doi.org/10.1534/g3.117.300331
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author Hoopes, Genevieve M.
Hamilton, John P.
Kim, Jeongwoon
Zhao, Dongyan
Wiegert-Rininger, Krystle
Crisovan, Emily
Buell, C. Robin
author_facet Hoopes, Genevieve M.
Hamilton, John P.
Kim, Jeongwoon
Zhao, Dongyan
Wiegert-Rininger, Krystle
Crisovan, Emily
Buell, C. Robin
author_sort Hoopes, Genevieve M.
collection PubMed
description Calotropis gigantea produces specialized secondary metabolites known as cardenolides, which have anticancer and antimalarial properties. Although transcriptomic studies have been conducted in other cardenolide-producing species, no nuclear genome assembly for an Asterid cardenolide-producing species has been reported to date. A high-quality de novo assembly was generated for C. gigantea, representing 157,284,427 bp with an N50 scaffold size of 805,959 bp, for which quality assessments indicated a near complete representation of the genic space. Transcriptome data in the form of RNA-sequencing libraries from a developmental tissue series was generated to aid the annotation and construction of a gene expression atlas. Using an ab initio and evidence-driven gene annotation pipeline, 18,197 high-confidence genes were annotated. Homologous and syntenic relationships between C. gigantea and other species within the Apocynaceae family confirmed previously identified evolutionary relationships, and suggest the emergence or loss of the specialized cardenolide metabolites after the divergence of the Apocynaceae subfamilies. The C. gigantea genome assembly, annotation, and RNA-sequencing data provide a novel resource to study the cardenolide biosynthesis pathway, especially for understanding the evolutionary origin of cardenolides and the engineering of cardenolide production in heterologous organisms for existing and novel pharmaceutical applications.
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spelling pubmed-59197232018-04-27 Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides Hoopes, Genevieve M. Hamilton, John P. Kim, Jeongwoon Zhao, Dongyan Wiegert-Rininger, Krystle Crisovan, Emily Buell, C. Robin G3 (Bethesda) Genome Report Calotropis gigantea produces specialized secondary metabolites known as cardenolides, which have anticancer and antimalarial properties. Although transcriptomic studies have been conducted in other cardenolide-producing species, no nuclear genome assembly for an Asterid cardenolide-producing species has been reported to date. A high-quality de novo assembly was generated for C. gigantea, representing 157,284,427 bp with an N50 scaffold size of 805,959 bp, for which quality assessments indicated a near complete representation of the genic space. Transcriptome data in the form of RNA-sequencing libraries from a developmental tissue series was generated to aid the annotation and construction of a gene expression atlas. Using an ab initio and evidence-driven gene annotation pipeline, 18,197 high-confidence genes were annotated. Homologous and syntenic relationships between C. gigantea and other species within the Apocynaceae family confirmed previously identified evolutionary relationships, and suggest the emergence or loss of the specialized cardenolide metabolites after the divergence of the Apocynaceae subfamilies. The C. gigantea genome assembly, annotation, and RNA-sequencing data provide a novel resource to study the cardenolide biosynthesis pathway, especially for understanding the evolutionary origin of cardenolides and the engineering of cardenolide production in heterologous organisms for existing and novel pharmaceutical applications. Genetics Society of America 2017-12-12 /pmc/articles/PMC5919723/ /pubmed/29237703 http://dx.doi.org/10.1534/g3.117.300331 Text en Copyright © 2018 Hoopes et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Report
Hoopes, Genevieve M.
Hamilton, John P.
Kim, Jeongwoon
Zhao, Dongyan
Wiegert-Rininger, Krystle
Crisovan, Emily
Buell, C. Robin
Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides
title Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides
title_full Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides
title_fullStr Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides
title_full_unstemmed Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides
title_short Genome Assembly and Annotation of the Medicinal Plant Calotropis gigantea, a Producer of Anticancer and Antimalarial Cardenolides
title_sort genome assembly and annotation of the medicinal plant calotropis gigantea, a producer of anticancer and antimalarial cardenolides
topic Genome Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919723/
https://www.ncbi.nlm.nih.gov/pubmed/29237703
http://dx.doi.org/10.1534/g3.117.300331
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