Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers

The cultivar Ganoderma lucidum Hunong 5 was obtained using cross-breeding. Hunong 5 has high commercial value due to its high polysaccharide and triterpene content. This is the first report of using a DNA pooling method to develop a stable sequence characterized amplified region (SCAR) marker for ra...

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Main Authors: Wen-zheng CHAO, Chuan-hong TANG, Jing-song ZHANG, Ling YU, Honda Yoichi
Format: Article
Language:English
Published: Elsevier 2018-01-01
Series:Journal of Integrative Agriculture
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2095311917618252
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author Wen-zheng CHAO
Chuan-hong TANG
Jing-song ZHANG
Ling YU
Honda Yoichi
author_facet Wen-zheng CHAO
Chuan-hong TANG
Jing-song ZHANG
Ling YU
Honda Yoichi
author_sort Wen-zheng CHAO
collection DOAJ
description The cultivar Ganoderma lucidum Hunong 5 was obtained using cross-breeding. Hunong 5 has high commercial value due to its high polysaccharide and triterpene content. This is the first report of using a DNA pooling method to develop a stable sequence characterized amplified region (SCAR) marker for rapid identification of the G. lucidum Hunong 5 cultivar. The SCAR marker was developed by first generating and sequencing a distinctive inter simple sequence repeat (ISSR) fragment (882 bp) from G. lucidum Hunong 5 cultivar. A stable SCAR primer pair GLH5F/GLH5R were obtained to identify the cultivar and the SCAR marker is a DNA fragment of 773 bp.
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spelling doaj.art-77d1005a543148588809fc42242f550b2022-12-21T21:25:54ZengElsevierJournal of Integrative Agriculture2095-31192018-01-01171130138Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markersWen-zheng CHAO0Chuan-hong TANG1Jing-song ZHANG2Ling YU3Honda Yoichi4School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P.R.China; Key Laboratory of Edible Fungus Resources and Utilization (South), Ministry of Agriculture/National Engineering Research Center of Edible Fungi/National R&D Center for Edible Fungi Processing/Key Laboratory of Agriculture Genetics and Breeding of Shanghai, Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Shanghai 201403, P.R.ChinaKey Laboratory of Edible Fungus Resources and Utilization (South), Ministry of Agriculture/National Engineering Research Center of Edible Fungi/National R&D Center for Edible Fungi Processing/Key Laboratory of Agriculture Genetics and Breeding of Shanghai, Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Shanghai 201403, P.R.China; Laboratory of Forest Biochemistry, Graduate School of Agriculture, Kyoto University, Kyoto 6068502, Japan; Correspondence TANG Chuan-hongKey Laboratory of Edible Fungus Resources and Utilization (South), Ministry of Agriculture/National Engineering Research Center of Edible Fungi/National R&D Center for Edible Fungi Processing/Key Laboratory of Agriculture Genetics and Breeding of Shanghai, Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Shanghai 201403, P.R.China; ZHANG Jing-song, Tel: +86-21-62200746, Fax: +86-21-62201530School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P.R.ChinaLaboratory of Forest Biochemistry, Graduate School of Agriculture, Kyoto University, Kyoto 6068502, JapanThe cultivar Ganoderma lucidum Hunong 5 was obtained using cross-breeding. Hunong 5 has high commercial value due to its high polysaccharide and triterpene content. This is the first report of using a DNA pooling method to develop a stable sequence characterized amplified region (SCAR) marker for rapid identification of the G. lucidum Hunong 5 cultivar. The SCAR marker was developed by first generating and sequencing a distinctive inter simple sequence repeat (ISSR) fragment (882 bp) from G. lucidum Hunong 5 cultivar. A stable SCAR primer pair GLH5F/GLH5R were obtained to identify the cultivar and the SCAR marker is a DNA fragment of 773 bp.http://www.sciencedirect.com/science/article/pii/S2095311917618252DNA poolingGanoderma lucidumHunong 5 cultivarISSR markerSCAR marker
spellingShingle Wen-zheng CHAO
Chuan-hong TANG
Jing-song ZHANG
Ling YU
Honda Yoichi
Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers
Journal of Integrative Agriculture
DNA pooling
Ganoderma lucidum
Hunong 5 cultivar
ISSR marker
SCAR marker
title Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers
title_full Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers
title_fullStr Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers
title_full_unstemmed Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers
title_short Development of a stable SCAR marker for rapid identification of Ganoderma lucidum Hunong 5 cultivar using DNA pooling method and inter-simple sequence repeat markers
title_sort development of a stable scar marker for rapid identification of ganoderma lucidum hunong 5 cultivar using dna pooling method and inter simple sequence repeat markers
topic DNA pooling
Ganoderma lucidum
Hunong 5 cultivar
ISSR marker
SCAR marker
url http://www.sciencedirect.com/science/article/pii/S2095311917618252
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