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Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode

The taxonomy and nomenclature of Dracaena plants are much disputed, particularly for several Dracaena species in Asia. However, neither morphological features nor common DNA regions are ideal for identification of Dracaena spp. Meanwhile, although multiple Dracaena spp. are sources of the rare tradi...

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Autores principales: Zhang, Zhonglian, Zhang, Yue, Song, Meifang, Guan, Yanhong, Ma, Xiaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901964/
https://www.ncbi.nlm.nih.gov/pubmed/31849682
http://dx.doi.org/10.3389/fphar.2019.01441
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author Zhang, Zhonglian
Zhang, Yue
Song, Meifang
Guan, Yanhong
Ma, Xiaojun
author_facet Zhang, Zhonglian
Zhang, Yue
Song, Meifang
Guan, Yanhong
Ma, Xiaojun
author_sort Zhang, Zhonglian
collection PubMed
description The taxonomy and nomenclature of Dracaena plants are much disputed, particularly for several Dracaena species in Asia. However, neither morphological features nor common DNA regions are ideal for identification of Dracaena spp. Meanwhile, although multiple Dracaena spp. are sources of the rare traditional medicine dragon’s blood, the Pharmacopoeia of the People’s Republic of China has defined Dracaena cochinchinensis as the only source plant. The inaccurate identification of Dracaena spp. will inevitably affect the clinical efficacy of dragon’s blood. It is therefore important to find a better method to distinguish these species. Here, we report the complete chloroplast (CP) genomes of six Dracaena spp., D. cochinchinensis, D. cambodiana, D. angustifolia, D. terniflora, D. hokouensis, and D. elliptica, obtained through high-throughput Illumina sequencing. These CP genomes exhibited typical circular tetramerous structure, and their sizes ranged from 155,055 (D. elliptica) to 155,449 bp (D. cochinchinensis). The GC content of each CP genome was 37.5%. Furthermore, each CP genome contained 130 genes, including 84 protein-coding genes, 38 tRNA genes, and 8 rRNA genes. There were no potential coding or non-coding regions to distinguish these six species, but the maximum likelihood tree of the six Dracaena spp. and other related species revealed that the whole CP genome can be used as a super-barcode to identify these Dracaena spp. This study provides not only invaluable data for species identification and safe medical application of Dracaena but also an important reference and foundation for species identification and phylogeny of Liliaceae plants.
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spelling pubmed-69019642019-12-17 Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode Zhang, Zhonglian Zhang, Yue Song, Meifang Guan, Yanhong Ma, Xiaojun Front Pharmacol Pharmacology The taxonomy and nomenclature of Dracaena plants are much disputed, particularly for several Dracaena species in Asia. However, neither morphological features nor common DNA regions are ideal for identification of Dracaena spp. Meanwhile, although multiple Dracaena spp. are sources of the rare traditional medicine dragon’s blood, the Pharmacopoeia of the People’s Republic of China has defined Dracaena cochinchinensis as the only source plant. The inaccurate identification of Dracaena spp. will inevitably affect the clinical efficacy of dragon’s blood. It is therefore important to find a better method to distinguish these species. Here, we report the complete chloroplast (CP) genomes of six Dracaena spp., D. cochinchinensis, D. cambodiana, D. angustifolia, D. terniflora, D. hokouensis, and D. elliptica, obtained through high-throughput Illumina sequencing. These CP genomes exhibited typical circular tetramerous structure, and their sizes ranged from 155,055 (D. elliptica) to 155,449 bp (D. cochinchinensis). The GC content of each CP genome was 37.5%. Furthermore, each CP genome contained 130 genes, including 84 protein-coding genes, 38 tRNA genes, and 8 rRNA genes. There were no potential coding or non-coding regions to distinguish these six species, but the maximum likelihood tree of the six Dracaena spp. and other related species revealed that the whole CP genome can be used as a super-barcode to identify these Dracaena spp. This study provides not only invaluable data for species identification and safe medical application of Dracaena but also an important reference and foundation for species identification and phylogeny of Liliaceae plants. Frontiers Media S.A. 2019-11-29 /pmc/articles/PMC6901964/ /pubmed/31849682 http://dx.doi.org/10.3389/fphar.2019.01441 Text en Copyright © 2019 Zhang, Zhang, Song, Guan and Ma http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Zhang, Zhonglian
Zhang, Yue
Song, Meifang
Guan, Yanhong
Ma, Xiaojun
Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode
title Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode
title_full Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode
title_fullStr Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode
title_full_unstemmed Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode
title_short Species Identification of Dracaena Using the Complete Chloroplast Genome as a Super-Barcode
title_sort species identification of dracaena using the complete chloroplast genome as a super-barcode
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901964/
https://www.ncbi.nlm.nih.gov/pubmed/31849682
http://dx.doi.org/10.3389/fphar.2019.01441
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