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通过等位基因特异性双重 PCR 快速鉴定药物型和纤维型大麻。

Rapid identification of drug-type and fiber-type cannabis by allele specific duplex PCR.

机构信息

National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, Chiba 277-0882, Japan.

National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, Chiba 277-0882, Japan.

出版信息

Forensic Sci Int. 2021 Jan;318:110634. doi: 10.1016/j.forsciint.2020.110634. Epub 2020 Nov 26.

Abstract

Cannabis is classified into two types: drug-type cannabis, which is abused worldwide, and fiber-type cannabis, which is used for industrial purposes. The two types are a result of differences in the sequences of tetrahydrocannabinolic acid synthase (THCAS) and cannabidiolic acid synthase (CBDAS) genes. In the present study, we aimed to establish a PCR-based method to distinguish between drug-type and fiber-type cannabis by detecting the differences in the sequences of THCAS and CBDAS. We constructed a single-plex PCR targeting active THCAS, and observed drug-type cannabis-specific amplification when using 10pg to 1ng of DNA; however, amplification was also observed in fiber-type cannabis when the DNA content reached 10ng. Similarly, single-plex PCR targeting active CBDAS showed fiber-type cannabis-specific amplification in 100pg of DNA, as well as in >1ng of drug-type cannabis DNA. Therefore, when an allele-specific duplex PCR system was constructed, in which both primer sets were mixed at an appropriate ratio, unintended nonspecific amplification was suppressed and amplicons of different sizes were observed between the drug-type and fiber-type cannabis, using DNA samples in the range of 1pg to 10ng. When the constructed duplex PCR was performed on DNA extracted from various cannabis seed samples, it was possible to distinguish between the drug-type and the fiber-type as well as detect a hybrid-type with both active THCAS and active CBDAS and a special type with neither. The identification method developed in the present study can quickly and accurately distinguish between drug-type and fiber-type cannabis, and is expected to be used for various purposes such as the detection of genetic contamination of industrial hemp as well as forensic examination of cannabis-related cases.

摘要

大麻被分为两种类型

滥用于全世界的毒品型大麻,以及用于工业目的的纤维型大麻。这两种类型是四氢大麻酸合成酶(THCAS)和大麻二酚酸合成酶(CBDAS)基因序列差异的结果。在本研究中,我们旨在建立一种基于 PCR 的方法,通过检测 THCAS 和 CBDAS 序列的差异来区分毒品型和纤维型大麻。我们构建了一种针对活性 THCAS 的单重 PCR,当使用 10pg 至 1ng 的 DNA 时,观察到毒品型大麻的特异性扩增;然而,当 DNA 含量达到 10ng 时,纤维型大麻也观察到了扩增。同样,针对活性 CBDAS 的单重 PCR 在 100pg 的 DNA 中显示出纤维型大麻的特异性扩增,以及超过 1ng 的毒品型大麻 DNA。因此,当构建等位基因特异性双重 PCR 系统时,在适当比例下混合两组引物,抑制了非特异性扩增,并在毒品型和纤维型大麻之间观察到不同大小的扩增子。使用 1pg 至 10ng 的 DNA 样本。当在所提取的各种大麻种子样本的 DNA 上进行构建的双重 PCR 时,能够区分毒品型和纤维型,并能够检测到具有活性 THCAS 和活性 CBDAS 的杂种型以及既没有活性 THCAS 也没有活性 CBDAS 的特殊型。本研究中开发的鉴定方法可以快速准确地区分毒品型和纤维型大麻,有望用于各种目的,例如检测工业大麻的遗传污染以及大麻相关案件的法医检查。

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