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采用抑制差减杂交技术对中药何首乌进行种属鉴定。

Species identification of Chinese medicinal plant Fallopia multiflora (Thunb.) Haraldson by suppression subtraction hybridization.

机构信息

School of Food Science, Guangdong Pharmaceutical University, Zhongshan, 528458, China,

出版信息

J Nat Med. 2014 Jan;68(1):192-8. doi: 10.1007/s11418-013-0772-1. Epub 2013 Apr 30.

Abstract

Fallopia multiflora (Thunb.) Haraldson, a traditional Chinese medicinal plant, has been extensively used in preparations of herbal medicine, health products and personal hygiene products. However, the clinical safety and efficiency of F. multiflora (Thunb.) Haraldson is impaired because of the existence of various adulterants. In this study, genomic DNA (gDNA) suppression subtraction hybridization (SSH) was used to authenticate F. multiflora (Thunb.) Haraldson from its adulterants. First, differential gDNA fragments between F. multiflora (Thunb.) Haraldson and its most closely related species F. multiflora var. ciliinervis (Nakai) Yonek. & H. Ohashi by SSH were identified. The differential fragments were then hybridized with arrays constructed from multiple whole genomes of several species (adulterants and/or closely related plants) to screen for the unique gDNA fragments representing F. multiflora (Thunb.) Haraldson. The unique gDNA fragments could be used to design species-specific primers for the identification of F. multiflora (Thunb.) Haraldson. Using SSH, we obtained four differential gDNA fragments, and four pairs of primers were designed. The designed primers could differentiate F. multiflora (Thunb.) Haraldson from its adulterants and/or closely related species via PCR. The results confirmed that the SSH is an efficient method for screening and designing species-specific primers.

摘要

何首乌(Thunb.) Haraldson 是一种传统的中药材,广泛应用于草药制剂、保健品和个人卫生用品。然而,由于存在各种掺杂物,何首乌(Thunb.) Haraldson 的临床安全性和效率受到影响。在本研究中,使用基因组 DNA(gDNA)抑制差减杂交(SSH)技术从掺杂物中鉴定何首乌(Thunb.) Haraldson。首先,通过 SSH 鉴定何首乌(Thunb.) Haraldson与其最密切相关的物种何首乌(Thunb.) Haraldson 的差异 gDNA 片段var. ciliinervis(Nakai)Yonek. & H. Ohashi。然后,将差异片段与来自多个物种(掺杂物和/或密切相关的植物)的多个全基因组构建的阵列杂交,以筛选代表何首乌(Thunb.) Haraldson 的独特 gDNA 片段。独特的 gDNA 片段可用于设计用于鉴定何首乌(Thunb.) Haraldson 的物种特异性引物。通过 SSH,我们获得了四个差异 gDNA 片段,并设计了四对引物。设计的引物可通过 PCR 将何首乌(Thunb.) Haraldson 与其掺杂物和/或密切相关的物种区分开来。结果证实 SSH 是筛选和设计物种特异性引物的有效方法。

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