2020
DOI: 10.1007/s13205-020-02325-y
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SCAR marker for identification and discrimination of specific medicinal Lycium chinense Miller from Lycium species from ramp-PCR RAPD fragments

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Cited by 16 publications
(5 citation statements)
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“…In the present study, a specific SCAR marker was developed for the authentication of ‘Daboju,’ based on SCoT analysis. In recent years, SCAR markers have increasingly been used for the authentication of medicinal plants, such as Ocimum tenuiflorum [ 33 ], Trapa natans [ 42 ], Lycium chinense [ 43 ], and Dendrobium officinale [ 36 ]. In addition, SCAR markers have also been used to identify adulterants in commercially important plant-derived food and medicinal products, such as Crocus sativus [ 44 ], Aconitum heterophyllum and Cyperus rotundus [ 37 ], Punica granatum [ 30 ], and Panax ginseng [ 45 ].…”
Section: Discussionmentioning
confidence: 99%
“…In the present study, a specific SCAR marker was developed for the authentication of ‘Daboju,’ based on SCoT analysis. In recent years, SCAR markers have increasingly been used for the authentication of medicinal plants, such as Ocimum tenuiflorum [ 33 ], Trapa natans [ 42 ], Lycium chinense [ 43 ], and Dendrobium officinale [ 36 ]. In addition, SCAR markers have also been used to identify adulterants in commercially important plant-derived food and medicinal products, such as Crocus sativus [ 44 ], Aconitum heterophyllum and Cyperus rotundus [ 37 ], Punica granatum [ 30 ], and Panax ginseng [ 45 ].…”
Section: Discussionmentioning
confidence: 99%
“…In 2000, molecular markers such as RAPD were first applied in Lycium species for the validation of the genetic diversity of L. barbarum (Cheng et al, 2000), while RAPD was also validated for its feasibility to distinguish close species of Lycium (Zhang et al, 2001). To date, simple sequence repeat (SSR), conserved ortholog set II (COSII), characterized amplified region (SCAR), amplified fragment length polymorphism (AFLP), restriction site−associated DNA sequencing (RADseq), internal transcribed spacer (ITS), sequence-related amplified polymorphism (SRAP), intersimple sequence repeat (ISSR), and random amplified, microsatellite polymorphism (RAMP)-PCR markers have been applied in genetic diversity, population structure, morphological variation, phylogenetic inference, traceability, and cultivar/species identification and discrimination (Zhang et al, 2001(Zhang et al, , 2018Yin et al, 2005;Sze et al, 2008;Chung et al, 2009;Kwon et al, 2009;Levin et al, 2009;Zhao et al, 2010;Balasubramani et al, 2011;Liu et al, 2012Liu et al, , 2020bTripathi, 2013;Xin et al, 2013;Chen and Zhong, 2014;Wang et al, 2015a;Chen J. et al, 2017;McCulloch et al, 2020;Jung et al, 2021). SSR markers can be used for the detection of genetic polymorphisms of species, calculation of genetic relationships (genetic distance) between varieties, identification of cultivars, and even construction of genetic maps and QTL mapping with sufficient SSR markers Essid et al, 2015;Ibrahim et al, 2016;Thammina et al, 2017;Portis et al, 2018b).…”
Section: Genetic Marker Developmentmentioning
confidence: 99%
“…This supports the applicability of the method for the distinction of different species, and moreover, reveals adulteration within commercial products. Recently, Liu, Cheng, et al (2020) continued the aforementioned studies by developing a novel RAPD-based SCAR marker specific for the medicinal L. chinense Miller in order to separate it from other Lycium species, as well as from its common adulterant species Nitraria sibirica Pall. The newly designed primers were specific to only L. chinense and therefore allowed to distinguish it from the other species.…”
Section: Pcr-based Techniquesmentioning
confidence: 99%