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MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens
MSH2 is a central component of the mismatch repair pathway that targets mismatches arising during DNA replication, homologous recombination (HR) and in response to genotoxic stresses. Here, we describe the function of MSH2 in the moss Physcomitrella patens, as deciphered by the analysis of loss of f...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1325206/ https://www.ncbi.nlm.nih.gov/pubmed/16397301 http://dx.doi.org/10.1093/nar/gkj423 |
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author | Trouiller, Bénédicte Schaefer, Didier G. Charlot, Florence Nogué, Fabien |
author_facet | Trouiller, Bénédicte Schaefer, Didier G. Charlot, Florence Nogué, Fabien |
author_sort | Trouiller, Bénédicte |
collection | PubMed |
description | MSH2 is a central component of the mismatch repair pathway that targets mismatches arising during DNA replication, homologous recombination (HR) and in response to genotoxic stresses. Here, we describe the function of MSH2 in the moss Physcomitrella patens, as deciphered by the analysis of loss of function mutants. Ppmsh2 mutants display pleiotropic growth and developmental defects, which reflect genomic instability. Based on loss of function of the APT gene, we estimated this mutator phenotype to be at least 130 times higher in the mutants than in wild type. We also found that MSH2 is involved in some but not all the moss responses to genotoxic stresses we tested. Indeed, the Ppmsh2 mutants were more tolerant to cisplatin and show higher sensitivity to UV-B radiations. PpMSH2 gene involvement in HR was studied by assessing gene targeting (GT) efficiency with homologous and homeologous sequences. GT efficiency with homologous sequences was slightly decreased in the Ppmsh2 mutant compared with wild type. Strikingly GT efficiency with homeologous sequences decreased proportionally to sequence divergence in the wild type whereas it remained unaffected in the mutants. Those results demonstrate the role of PpMSH2 in the maintenance of genome integrity and in homologous and homeologous recombination. |
format | Text |
id | pubmed-1325206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-13252062006-01-17 MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens Trouiller, Bénédicte Schaefer, Didier G. Charlot, Florence Nogué, Fabien Nucleic Acids Res Article MSH2 is a central component of the mismatch repair pathway that targets mismatches arising during DNA replication, homologous recombination (HR) and in response to genotoxic stresses. Here, we describe the function of MSH2 in the moss Physcomitrella patens, as deciphered by the analysis of loss of function mutants. Ppmsh2 mutants display pleiotropic growth and developmental defects, which reflect genomic instability. Based on loss of function of the APT gene, we estimated this mutator phenotype to be at least 130 times higher in the mutants than in wild type. We also found that MSH2 is involved in some but not all the moss responses to genotoxic stresses we tested. Indeed, the Ppmsh2 mutants were more tolerant to cisplatin and show higher sensitivity to UV-B radiations. PpMSH2 gene involvement in HR was studied by assessing gene targeting (GT) efficiency with homologous and homeologous sequences. GT efficiency with homologous sequences was slightly decreased in the Ppmsh2 mutant compared with wild type. Strikingly GT efficiency with homeologous sequences decreased proportionally to sequence divergence in the wild type whereas it remained unaffected in the mutants. Those results demonstrate the role of PpMSH2 in the maintenance of genome integrity and in homologous and homeologous recombination. Oxford University Press 2006 2006-01-05 /pmc/articles/PMC1325206/ /pubmed/16397301 http://dx.doi.org/10.1093/nar/gkj423 Text en © The Author 2006. Published by Oxford University Press. All rights reserved |
spellingShingle | Article Trouiller, Bénédicte Schaefer, Didier G. Charlot, Florence Nogué, Fabien MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
title | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
title_full | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
title_fullStr | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
title_full_unstemmed | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
title_short | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
title_sort | msh2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss physcomitrella patens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1325206/ https://www.ncbi.nlm.nih.gov/pubmed/16397301 http://dx.doi.org/10.1093/nar/gkj423 |
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