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p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues

The effect of p53‐deficiency on somatic mutation of minisatellites in normal tissues was examined using p53‐deficient (−/−) mice. In total, 248 mice consisting of three different genotypes, +/+, +/− and −/−, were obtained and DNA from their embryos was probed with two minisatellites, Pc‐1 and Pc‐2....

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Detalles Bibliográficos
Autores principales: Ohashi, Manabu, Hatakeyama, Katsuyoshi, Aizawa, Shinichi, Kominami, Ryo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921163/
https://www.ncbi.nlm.nih.gov/pubmed/8698618
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00280.x
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author Ohashi, Manabu
Hatakeyama, Katsuyoshi
Aizawa, Shinichi
Kominami, Ryo
author_facet Ohashi, Manabu
Hatakeyama, Katsuyoshi
Aizawa, Shinichi
Kominami, Ryo
author_sort Ohashi, Manabu
collection PubMed
description The effect of p53‐deficiency on somatic mutation of minisatellites in normal tissues was examined using p53‐deficient (−/−) mice. In total, 248 mice consisting of three different genotypes, +/+, +/− and −/−, were obtained and DNA from their embryos was probed with two minisatellites, Pc‐1 and Pc‐2. The somatic mutation was detected by Southern blot hybridization as the presence of a third nonparental band reflecting mosaicism in tissues. Mutation frequency of Pc‐1 for (+/+) and (+/−) was 1.3% and 1.4%, respectively, which is consistent with previous studies. On the other hand, none of the mice lacking the p53 gene (−/−) exhibited mutation. The Pc‐2 probe did not show any somatic mutation in the three groups. These results suggest that the p53 deficiency does not enhance the genomic instability of the minisatellite loci in normal somatic cells.
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spelling pubmed-59211632018-05-11 p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues Ohashi, Manabu Hatakeyama, Katsuyoshi Aizawa, Shinichi Kominami, Ryo Jpn J Cancer Res Article The effect of p53‐deficiency on somatic mutation of minisatellites in normal tissues was examined using p53‐deficient (−/−) mice. In total, 248 mice consisting of three different genotypes, +/+, +/− and −/−, were obtained and DNA from their embryos was probed with two minisatellites, Pc‐1 and Pc‐2. The somatic mutation was detected by Southern blot hybridization as the presence of a third nonparental band reflecting mosaicism in tissues. Mutation frequency of Pc‐1 for (+/+) and (+/−) was 1.3% and 1.4%, respectively, which is consistent with previous studies. On the other hand, none of the mice lacking the p53 gene (−/−) exhibited mutation. The Pc‐2 probe did not show any somatic mutation in the three groups. These results suggest that the p53 deficiency does not enhance the genomic instability of the minisatellite loci in normal somatic cells. Blackwell Publishing Ltd 1996-07 /pmc/articles/PMC5921163/ /pubmed/8698618 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00280.x Text en
spellingShingle Article
Ohashi, Manabu
Hatakeyama, Katsuyoshi
Aizawa, Shinichi
Kominami, Ryo
p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues
title p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues
title_full p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues
title_fullStr p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues
title_full_unstemmed p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues
title_short p53 Gene Deficiency Does Not Enhance Instability of Mouse Minisatellites in Somatic Cells of Normal Tissues
title_sort p53 gene deficiency does not enhance instability of mouse minisatellites in somatic cells of normal tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921163/
https://www.ncbi.nlm.nih.gov/pubmed/8698618
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00280.x
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