SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.

Amomum villosum Lour., produced from Yangchun, Guangdong Province, China, is a Daodi medicinal material of Amomi Fructus in traditional Chinese medicine. This herb germplasm should be accurately identified and collected to ensure its quality and safety in medication. In the present study, single nuc...

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Main Authors: Qionglin Huang, Zhonggang Duan, Jinfen Yang, Xinye Ma, Ruoting Zhan, Hui Xu, Weiwen Chen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4274006?pdf=render
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spelling doaj-d19d499756d74b99b319062bc9d22cd52020-11-25T01:45:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11494010.1371/journal.pone.0114940SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.Qionglin HuangZhonggang DuanJinfen YangXinye MaRuoting ZhanHui XuWeiwen ChenAmomum villosum Lour., produced from Yangchun, Guangdong Province, China, is a Daodi medicinal material of Amomi Fructus in traditional Chinese medicine. This herb germplasm should be accurately identified and collected to ensure its quality and safety in medication. In the present study, single nucleotide polymorphism typing method was evaluated on the basis of DNA barcoding markers to identify the germplasm of Amomi Fructus. Genomic DNA was extracted from the leaves of 29 landraces representing three Amomum species (A. villosum Lour., A. xanthioides Wall. ex Baker and A. longiligulare T. L. Wu) by using the CTAB method. Six barcoding markers (ITS, ITS2, LSU D1-D3, matK, rbcL and trnH-psbA) were PCR amplified and sequenced; SNP typing and phylogenetic analysis were performed to differentiate the landraces. Results showed that high-quality bidirectional sequences were acquired for five candidate regions (ITS, ITS2, LSU D1-D3, matK, and rbcL) except trnH-psbA. Three ribosomal regions, namely, ITS, ITS2, and LSU D1-D3, contained more SNP genotypes (STs) than the plastid genes rbcL and matK. In the 29 specimens, 19 STs were detected from the combination of four regions (ITS, LSU D1-D3, rbcL, and matK). Phylogenetic analysis results further revealed two clades. Minimum-spanning tree demonstrated the existence of two main groups: group I was consisting of 9 STs (ST1-8 and ST11) of A. villosum Lour., and group II was composed of 3 STs (ST16-18) of A. longiligulare T.L. Wu. Our results suggested that ITS and LSU D1-D3 should be incorporated with the core barcodes rbcL and matK. The four combined regions could be used as a multiregional DNA barcode to precisely differentiate the Amomi Fructus landraces in different producing areas.http://europepmc.org/articles/PMC4274006?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Qionglin Huang
Zhonggang Duan
Jinfen Yang
Xinye Ma
Ruoting Zhan
Hui Xu
Weiwen Chen
spellingShingle Qionglin Huang
Zhonggang Duan
Jinfen Yang
Xinye Ma
Ruoting Zhan
Hui Xu
Weiwen Chen
SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.
PLoS ONE
author_facet Qionglin Huang
Zhonggang Duan
Jinfen Yang
Xinye Ma
Ruoting Zhan
Hui Xu
Weiwen Chen
author_sort Qionglin Huang
title SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.
title_short SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.
title_full SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.
title_fullStr SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.
title_full_unstemmed SNP typing for germplasm identification of Amomum villosum Lour. Based on DNA barcoding markers.
title_sort snp typing for germplasm identification of amomum villosum lour. based on dna barcoding markers.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Amomum villosum Lour., produced from Yangchun, Guangdong Province, China, is a Daodi medicinal material of Amomi Fructus in traditional Chinese medicine. This herb germplasm should be accurately identified and collected to ensure its quality and safety in medication. In the present study, single nucleotide polymorphism typing method was evaluated on the basis of DNA barcoding markers to identify the germplasm of Amomi Fructus. Genomic DNA was extracted from the leaves of 29 landraces representing three Amomum species (A. villosum Lour., A. xanthioides Wall. ex Baker and A. longiligulare T. L. Wu) by using the CTAB method. Six barcoding markers (ITS, ITS2, LSU D1-D3, matK, rbcL and trnH-psbA) were PCR amplified and sequenced; SNP typing and phylogenetic analysis were performed to differentiate the landraces. Results showed that high-quality bidirectional sequences were acquired for five candidate regions (ITS, ITS2, LSU D1-D3, matK, and rbcL) except trnH-psbA. Three ribosomal regions, namely, ITS, ITS2, and LSU D1-D3, contained more SNP genotypes (STs) than the plastid genes rbcL and matK. In the 29 specimens, 19 STs were detected from the combination of four regions (ITS, LSU D1-D3, rbcL, and matK). Phylogenetic analysis results further revealed two clades. Minimum-spanning tree demonstrated the existence of two main groups: group I was consisting of 9 STs (ST1-8 and ST11) of A. villosum Lour., and group II was composed of 3 STs (ST16-18) of A. longiligulare T.L. Wu. Our results suggested that ITS and LSU D1-D3 should be incorporated with the core barcodes rbcL and matK. The four combined regions could be used as a multiregional DNA barcode to precisely differentiate the Amomi Fructus landraces in different producing areas.
url http://europepmc.org/articles/PMC4274006?pdf=render
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