Osawa Yuko, Ikebukuro Kazunori, Motoki Hiroaki, Matsuo Takafumi, Horiuchi Michio, Sode Koji
Department of Biotechnology and Life Science, Tokyo University of Agriculture & Technology, 2-24-16 Naka-cho, Koganei, 184-8588 Tokyo, Japan.
Nucleic Acids Res. 2008 Jun;36(11):e68. doi: 10.1093/nar/gkn274. Epub 2008 May 23.
A novel method of rapid and specific detection of polymerase chain reaction (PCR) products from bacterial genomes using Zn finger proteins was developed. Zn finger proteins are DNA-binding proteins that can sequence specifically recognize PCR products. Since Zn finger proteins can directly detect PCR products without undergoing dehybridization, unlike probe DNA, and can double check the specific PCR amplification and sequence specificity of the PCR products, this novel method would be quick and highly accurate. In this study, we tried to detect Legionella pneumophila using Sp1. It was found that a 49 bp L. pneumophila-specific region containing the Sp1 recognition site is located on the flhA gene of the L. pneumophila genome. We succeeded in specifically detecting PCR products amplified from L. pneumophila in the presence of other bacterial genomes by ELISA, and demonstrated that Sp1 enables the discrimination of L. pneumophila-specific PCR products from others. By fluorescence depolarization measurement, these specific PCR products could be detected within 1 min. These results indicate that the rapid and simple detection of PCR products specific to L. pneumophila using a Zn finger protein was achieved. This methodology can be applied to the detection of other bacteria using various Zn finger proteins that have already been reported.
开发了一种使用锌指蛋白快速、特异性检测细菌基因组聚合酶链反应(PCR)产物的新方法。锌指蛋白是一种DNA结合蛋白,能够特异性识别PCR产物的序列。由于锌指蛋白与探针DNA不同,无需进行解杂交就能直接检测PCR产物,并且可以对PCR产物的特异性PCR扩增和序列特异性进行双重检查,因此这种新方法快速且高度准确。在本研究中,我们尝试使用Sp1检测嗜肺军团菌。结果发现,嗜肺军团菌基因组的flhA基因上存在一个包含Sp1识别位点的49 bp嗜肺军团菌特异性区域。我们通过酶联免疫吸附测定(ELISA)成功地在存在其他细菌基因组的情况下特异性检测了从嗜肺军团菌扩增的PCR产物,并证明Sp1能够区分嗜肺军团菌特异性PCR产物与其他产物。通过荧光偏振测量,这些特异性PCR产物可在1分钟内被检测到。这些结果表明,利用锌指蛋白实现了对嗜肺军团菌特异性PCR产物的快速、简便检测。该方法可应用于使用已报道的各种锌指蛋白检测其他细菌。