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Establishment of Methylation-Specific PCR for the Mouse p53 Gene
Methylation-specific PCR (MSP) of the mouse p53 gene has not yet been reported. We searched the CpG islands, sequenced the bisulfited DNA, and designed PCR primers for methylation and unmethylation sites. DNA from a young mouse produced a strong PCR product with the unmethylated primer and a weaker...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE-Hindawi Access to Research
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238407/ https://www.ncbi.nlm.nih.gov/pubmed/22203902 http://dx.doi.org/10.4061/2011/938435 |
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author | Okazaki, Ryuji Ootsuyama, Akira Yoshida, Yasuhiro Norimura, Toshiyuki |
author_facet | Okazaki, Ryuji Ootsuyama, Akira Yoshida, Yasuhiro Norimura, Toshiyuki |
author_sort | Okazaki, Ryuji |
collection | PubMed |
description | Methylation-specific PCR (MSP) of the mouse p53 gene has not yet been reported. We searched the CpG islands, sequenced the bisulfited DNA, and designed PCR primers for methylation and unmethylation sites. DNA from a young mouse produced a strong PCR product with the unmethylated primer and a weaker band with the methylated primer. DNA from an old mouse produced bands of similar intensities with both primers. In radiation-induced tumors, DNA from an old mouse yielded similar bands with both types of primers. We suggest that MSP is a valuable technique for the epigenetic study of the mouse p53 gene. |
format | Online Article Text |
id | pubmed-3238407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SAGE-Hindawi Access to Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-32384072011-12-27 Establishment of Methylation-Specific PCR for the Mouse p53 Gene Okazaki, Ryuji Ootsuyama, Akira Yoshida, Yasuhiro Norimura, Toshiyuki Mol Biol Int Research Article Methylation-specific PCR (MSP) of the mouse p53 gene has not yet been reported. We searched the CpG islands, sequenced the bisulfited DNA, and designed PCR primers for methylation and unmethylation sites. DNA from a young mouse produced a strong PCR product with the unmethylated primer and a weaker band with the methylated primer. DNA from an old mouse produced bands of similar intensities with both primers. In radiation-induced tumors, DNA from an old mouse yielded similar bands with both types of primers. We suggest that MSP is a valuable technique for the epigenetic study of the mouse p53 gene. SAGE-Hindawi Access to Research 2011 2011-12-12 /pmc/articles/PMC3238407/ /pubmed/22203902 http://dx.doi.org/10.4061/2011/938435 Text en Copyright © 2011 Ryuji Okazaki et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Okazaki, Ryuji Ootsuyama, Akira Yoshida, Yasuhiro Norimura, Toshiyuki Establishment of Methylation-Specific PCR for the Mouse p53 Gene |
title | Establishment of Methylation-Specific PCR for the Mouse p53 Gene |
title_full | Establishment of Methylation-Specific PCR for the Mouse p53 Gene |
title_fullStr | Establishment of Methylation-Specific PCR for the Mouse p53 Gene |
title_full_unstemmed | Establishment of Methylation-Specific PCR for the Mouse p53 Gene |
title_short | Establishment of Methylation-Specific PCR for the Mouse p53 Gene |
title_sort | establishment of methylation-specific pcr for the mouse p53 gene |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238407/ https://www.ncbi.nlm.nih.gov/pubmed/22203902 http://dx.doi.org/10.4061/2011/938435 |
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