Comparative study on chloroplast genomes of three Hansenia forbesii varieties (Apiaceae)

To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp) genome of these three varieties were firstly sequencing by the Illumina hiseq platform. In this study, we assembled the complete cp genome se...

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Published inPloS one Vol. 18; no. 6; p. e0286587
Main Authors Zhu, Chenghao, Jiang, Yuan, Bai, Yu, Dong, Shengjian, Zhirong, Sun
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 01.06.2023
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Abstract To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp) genome of these three varieties were firstly sequencing by the Illumina hiseq platform. In this study, we assembled the complete cp genome sequences of Hansenia forbesii LQ (156,954 bp), H. forbesii QX (157,181 bp), H. forbesii WQ (156,975 bp). They all contained 84 protein-coding genes, 37 tRNAs, and 8 rRNAs. The hypervariable regions between three cp genomes were atpF-atpH, petD, and rps15-ycf1. Phylogenetic analysis showed that H. forbesii LQ and H. forbesii WQ were closely related, followed by H. forbesii QX. This study showed that the three varieties of H. forbesii could be identified by the complete cp genome and specific DNA barcode (trnC-GCA-petN) and provided a new idea for germplasm identification of similar cultivated varieties.
AbstractList To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp) genome of these three varieties were firstly sequencing by the Illumina hiseq platform. In this study, we assembled the complete cp genome sequences of Hansenia forbesii LQ (156,954 bp), H. forbesii QX (157,181 bp), H. forbesii WQ (156,975 bp). They all contained 84 protein-coding genes, 37 tRNAs, and 8 rRNAs. The hypervariable regions between three cp genomes were atpF-atpH, petD, and rps15-ycf1. Phylogenetic analysis showed that H. forbesii LQ and H. forbesii WQ were closely related, followed by H. forbesii QX. This study showed that the three varieties of H. forbesii could be identified by the complete cp genome and specific DNA barcode (trnC-GCA-petN) and provided a new idea for germplasm identification of similar cultivated varieties.
To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp) genome of these three varieties were firstly sequencing by the Illumina hiseq platform. In this study, we assembled the complete cp genome sequences of Hansenia forbesii LQ (156,954 bp), H . forbesii QX (157,181 bp), H . forbesii WQ (156,975 bp). They all contained 84 protein-coding genes, 37 tRNAs, and 8 rRNAs. The hypervariable regions between three cp genomes were atp F- atp H, pet D, and rps 15- ycf 1. Phylogenetic analysis showed that H . forbesii LQ and H . forbesii WQ were closely related, followed by H . forbesii QX. This study showed that the three varieties of H . forbesii could be identified by the complete cp genome and specific DNA barcode ( trn C-GCA- pet N) and provided a new idea for germplasm identification of similar cultivated varieties.
To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp) genome of these three varieties were firstly sequencing by the Illumina hiseq platform. In this study, we assembled the complete cp genome sequences of Hansenia forbesii LQ (156,954 bp), H . forbesii QX (157,181 bp), H . forbesii WQ (156,975 bp). They all contained 84 protein-coding genes, 37 tRNAs, and 8 rRNAs. The hypervariable regions between three cp genomes were atp F- atp H, pet D, and rps 15- ycf 1. Phylogenetic analysis showed that H . forbesii LQ and H . forbesii WQ were closely related, followed by H . forbesii QX. This study showed that the three varieties of H . forbesii could be identified by the complete cp genome and specific DNA barcode ( trn C-GCA- pet N) and provided a new idea for germplasm identification of similar cultivated varieties.
Audience Academic
Author Dong, Shengjian
Zhirong, Sun
Zhu, Chenghao
Jiang, Yuan
Bai, Yu
AuthorAffiliation 2 College of Applied Technology, Gansu Agricultural University. Lanzhou, Gansu, China
1 School of Chinese Materia Medica, Beijing University of Chinese Medicine. Beijing, Beijing, China
Texas A&M University and Texas A&M Agrilife Research, UNITED STATES
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2023 Zhu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Snippet To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp)...
To find the gene hypervariable regions of three varieties of Hansenia forbesii H. Boissieu and determine their phylogenetic relationship, the chloroplast (cp)...
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StartPage e0286587
SubjectTerms Analysis
Apiaceae
Biology and Life Sciences
Biotechnology
Chinese medicine
Chloroplasts
Comparative studies
Computer and Information Sciences
Control
Deoxyribonucleic acid
DNA
Endangered species
Engineering and Technology
Gene sequencing
Genes
Genetic aspects
Genetic engineering
Genetic testing
Genomes
Genomics
Germplasm
Identification and classification
Phylogenetics
Phylogeny
Protection and preservation
Research and Analysis Methods
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Title Comparative study on chloroplast genomes of three Hansenia forbesii varieties (Apiaceae)
URI https://www.ncbi.nlm.nih.gov/pubmed/37262084
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https://pubmed.ncbi.nlm.nih.gov/PMC10234559
https://doaj.org/article/4478bc54ee9b428480d2934c34e83811
http://dx.doi.org/10.1371/journal.pone.0286587
Volume 18
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