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Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification

The genus Angelica (Apiaceae) comprises valuable herbal medicines. In this study, we determined the complete chloroplast (CP) genome sequence of A. polymorpha and compared it with that of Ligusticum officinale (GenBank accession no. NC039760). The CP genomes of A. polymorpha and L. officinale were 1...

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Autores principales: Park, Inkyu, Yang, Sungyu, Kim, Wook Jin, Song, Jun-Ho, Lee, Hyun-Sook, Lee, Hyun Oh, Lee, Jung-Hyun, Ahn, Sang-Nag, Moon, Byeong Cheol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471784/
https://www.ncbi.nlm.nih.gov/pubmed/30875988
http://dx.doi.org/10.3390/molecules24061038
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author Park, Inkyu
Yang, Sungyu
Kim, Wook Jin
Song, Jun-Ho
Lee, Hyun-Sook
Lee, Hyun Oh
Lee, Jung-Hyun
Ahn, Sang-Nag
Moon, Byeong Cheol
author_facet Park, Inkyu
Yang, Sungyu
Kim, Wook Jin
Song, Jun-Ho
Lee, Hyun-Sook
Lee, Hyun Oh
Lee, Jung-Hyun
Ahn, Sang-Nag
Moon, Byeong Cheol
author_sort Park, Inkyu
collection PubMed
description The genus Angelica (Apiaceae) comprises valuable herbal medicines. In this study, we determined the complete chloroplast (CP) genome sequence of A. polymorpha and compared it with that of Ligusticum officinale (GenBank accession no. NC039760). The CP genomes of A. polymorpha and L. officinale were 148,430 and 147,127 bp in length, respectively, with 37.6% GC content. Both CP genomes harbored 113 unique functional genes, including 79 protein-coding, four rRNA, and 30 tRNA genes. Comparative analysis of the two CP genomes revealed conserved genome structure, gene content, and gene order. However, highly variable regions, sufficient to distinguish between A. polymorpha and L. officinale, were identified in hypothetical chloroplast open reading frame1 (ycf1) and ycf2 genic regions. Nucleotide diversity (Pi) analysis indicated that ycf4–chloroplast envelope membrane protein (cemA) intergenic region was highly variable between the two species. Phylogenetic analysis revealed that A. polymorpha and L. officinale were well clustered at family Apiaceae. The ycf4-cemA intergenic region in A. polymorpha carried a 418 bp deletion compared with L. officinale. This region was used for the development of a novel indel marker, LYCE, which successfully discriminated between A. polymorpha and L. officinale accessions. Our results provide important taxonomic and phylogenetic information on herbal medicines and facilitate their authentication using the indel marker.
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spelling pubmed-64717842019-04-26 Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification Park, Inkyu Yang, Sungyu Kim, Wook Jin Song, Jun-Ho Lee, Hyun-Sook Lee, Hyun Oh Lee, Jung-Hyun Ahn, Sang-Nag Moon, Byeong Cheol Molecules Article The genus Angelica (Apiaceae) comprises valuable herbal medicines. In this study, we determined the complete chloroplast (CP) genome sequence of A. polymorpha and compared it with that of Ligusticum officinale (GenBank accession no. NC039760). The CP genomes of A. polymorpha and L. officinale were 148,430 and 147,127 bp in length, respectively, with 37.6% GC content. Both CP genomes harbored 113 unique functional genes, including 79 protein-coding, four rRNA, and 30 tRNA genes. Comparative analysis of the two CP genomes revealed conserved genome structure, gene content, and gene order. However, highly variable regions, sufficient to distinguish between A. polymorpha and L. officinale, were identified in hypothetical chloroplast open reading frame1 (ycf1) and ycf2 genic regions. Nucleotide diversity (Pi) analysis indicated that ycf4–chloroplast envelope membrane protein (cemA) intergenic region was highly variable between the two species. Phylogenetic analysis revealed that A. polymorpha and L. officinale were well clustered at family Apiaceae. The ycf4-cemA intergenic region in A. polymorpha carried a 418 bp deletion compared with L. officinale. This region was used for the development of a novel indel marker, LYCE, which successfully discriminated between A. polymorpha and L. officinale accessions. Our results provide important taxonomic and phylogenetic information on herbal medicines and facilitate their authentication using the indel marker. MDPI 2019-03-15 /pmc/articles/PMC6471784/ /pubmed/30875988 http://dx.doi.org/10.3390/molecules24061038 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Park, Inkyu
Yang, Sungyu
Kim, Wook Jin
Song, Jun-Ho
Lee, Hyun-Sook
Lee, Hyun Oh
Lee, Jung-Hyun
Ahn, Sang-Nag
Moon, Byeong Cheol
Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification
title Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification
title_full Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification
title_fullStr Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification
title_full_unstemmed Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification
title_short Sequencing and Comparative Analysis of the Chloroplast Genome of Angelica polymorpha and the Development of a Novel Indel Marker for Species Identification
title_sort sequencing and comparative analysis of the chloroplast genome of angelica polymorpha and the development of a novel indel marker for species identification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471784/
https://www.ncbi.nlm.nih.gov/pubmed/30875988
http://dx.doi.org/10.3390/molecules24061038
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