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The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins
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 PC...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441800/ https://www.ncbi.nlm.nih.gov/pubmed/18502777 http://dx.doi.org/10.1093/nar/gkn274 |
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author | Osawa, Yuko Ikebukuro, Kazunori Motoki, Hiroaki Matsuo, Takafumi Horiuchi, Michio Sode, Koji |
author_facet | Osawa, Yuko Ikebukuro, Kazunori Motoki, Hiroaki Matsuo, Takafumi Horiuchi, Michio Sode, Koji |
author_sort | Osawa, Yuko |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2441800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24418002008-07-02 The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins Osawa, Yuko Ikebukuro, Kazunori Motoki, Hiroaki Matsuo, Takafumi Horiuchi, Michio Sode, Koji Nucleic Acids Res Methods Online 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. Oxford University Press 2008-06 2008-05-23 /pmc/articles/PMC2441800/ /pubmed/18502777 http://dx.doi.org/10.1093/nar/gkn274 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Osawa, Yuko Ikebukuro, Kazunori Motoki, Hiroaki Matsuo, Takafumi Horiuchi, Michio Sode, Koji The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins |
title | The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins |
title_full | The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins |
title_fullStr | The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins |
title_full_unstemmed | The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins |
title_short | The simple and rapid detection of specific PCR products from bacterial genomes using Zn finger proteins |
title_sort | simple and rapid detection of specific pcr products from bacterial genomes using zn finger proteins |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441800/ https://www.ncbi.nlm.nih.gov/pubmed/18502777 http://dx.doi.org/10.1093/nar/gkn274 |
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