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通过针对线粒体DNA的巢式PCR对动物细胞进行物种鉴定。

Species identification of animal cells by nested PCR targeted to mitochondrial DNA.

作者信息

Ono Kazumi, Satoh Motonobu, Yoshida Touho, Ozawa Yutaka, Kohara Arihiro, Takeuchi Masao, Mizusawa Hiroshi, Sawada Hidekazu

机构信息

Health Science Research Resources Bank (HSRRB), Japan Health Sciences Foundation, 2-11 Rinku-minamihama, Sennan-shi, Osaka 590-0535, Japan.

出版信息

In Vitro Cell Dev Biol Anim. 2007 May-Jun;43(5-6):168-75. doi: 10.1007/s11626-007-9033-5. Epub 2007 May 22.

Abstract

We developed a highly sensitive and convenient method of nested polymerase chain reaction (PCR) targeted to mitochondrial deoxyribonucleic acid (DNA) to identify animal species quickly in cultured cells. Fourteen vertebrate species, including human, cynomolgus monkey, African green monkey, mouse, rat, Syrian hamster, Chinese hamster, guinea pig, rabbit, dog, cat, cow, pig, and chicken, could be distinguished from each other by nested PCR. The first PCR amplifies mitochondrial DNA fragments with a universal primer pair complementary to the conserved regions of 14 species, and the second PCR amplifies the DNA fragments with species-specific primer pairs from the first products. The species-specific primer pairs were designed to easily distinguish 14 species from each other under standard agarose gel electrophoresis. We further developed the multiplex PCR using a mixture of seven species-specific primer pairs for two groups of animals. One was comprised of human, mouse, rat, cat, pig, cow, and rabbit, and the other was comprised of African green monkey, cynomolgus monkey, Syrian hamster, Chinese hamster, guinea pig, dog, and chicken. The sensitivity of the PCR assay was at least 100 pg DNA/reaction, which was sufficient for the detection of each species of DNA. Furthermore, the nested PCR method was able to identify the species in the interspecies mixture of DNA. Thus, the method developed in this study will provide a useful tool for the authentication of animal species.

摘要

我们开发了一种针对线粒体脱氧核糖核酸(DNA)的高灵敏度且便捷的巢式聚合酶链反应(PCR)方法,用于在培养细胞中快速鉴定动物物种。包括人类、食蟹猴、非洲绿猴、小鼠、大鼠、叙利亚仓鼠、中国仓鼠、豚鼠、兔子、狗、猫、牛、猪和鸡在内的14种脊椎动物物种,可通过巢式PCR相互区分。第一次PCR使用与14个物种保守区域互补的通用引物对扩增线粒体DNA片段,第二次PCR使用来自第一次产物的物种特异性引物对扩增DNA片段。物种特异性引物对的设计旨在能够在标准琼脂糖凝胶电泳下轻松区分这14个物种。我们进一步开发了多重PCR,使用两组动物的七种物种特异性引物对的混合物。一组由人类、小鼠、大鼠、猫、猪、牛和兔子组成,另一组由非洲绿猴、食蟹猴、叙利亚仓鼠、中国仓鼠、豚鼠、狗和鸡组成。PCR检测的灵敏度至少为100 pg DNA/反应,这足以检测每种DNA物种。此外,巢式PCR方法能够鉴定DNA种间混合物中的物种。因此,本研究中开发的方法将为动物物种鉴定提供一个有用的工具。

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