MutS and MutL are dispensable for maintenance of the genomic mutation rate in the halophilic archaeon Halobacterium salinarum NRC-1

The genome of the halophilic archaeon Halobacterium salinarum NRC-1 encodes for homologs of MutS and MutL, which are key proteins of a DNA mismatch repair pathway conserved in Bacteria and Eukarya. Mismatch repair is essential for retaining the fidelity of genetic information and defects in this pat...

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Veröffentlicht in:PloS one 2010-02, Vol.5 (2), p.e9045
Hauptverfasser: Busch, Courtney R, DiRuggiero, Jocelyne
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description The genome of the halophilic archaeon Halobacterium salinarum NRC-1 encodes for homologs of MutS and MutL, which are key proteins of a DNA mismatch repair pathway conserved in Bacteria and Eukarya. Mismatch repair is essential for retaining the fidelity of genetic information and defects in this pathway result in the deleterious accumulation of mutations and in hereditary diseases in humans. We calculated the spontaneous genomic mutation rate of H. salinarum NRC-1 using fluctuation tests targeting genes of the uracil monophosphate biosynthesis pathway. We found that H. salinarum NRC-1 has a low incidence of mutation suggesting the presence of active mechanisms to control spontaneous mutations during replication. The spectrum of mutational changes found in H. salinarum NRC-1, and in other archaea, appears to be unique to this domain of life and might be a consequence of their adaption to extreme environmental conditions. In-frame targeted gene deletions of H. salinarum NRC-1 mismatch repair genes and phenotypic characterization of the mutants demonstrated that the mutS and mutL genes are not required for maintenance of the observed mutation rate. We established that H. salinarum NRC-1 mutS and mutL genes are redundant to an alternative system that limits spontaneous mutation in this organism. This finding leads to the puzzling question of what mechanism is responsible for maintenance of the low genomic mutation rates observed in the Archaea, which for the most part do not have MutS and MutL homologs.
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Mismatch repair is essential for retaining the fidelity of genetic information and defects in this pathway result in the deleterious accumulation of mutations and in hereditary diseases in humans. We calculated the spontaneous genomic mutation rate of H. salinarum NRC-1 using fluctuation tests targeting genes of the uracil monophosphate biosynthesis pathway. We found that H. salinarum NRC-1 has a low incidence of mutation suggesting the presence of active mechanisms to control spontaneous mutations during replication. The spectrum of mutational changes found in H. salinarum NRC-1, and in other archaea, appears to be unique to this domain of life and might be a consequence of their adaption to extreme environmental conditions. In-frame targeted gene deletions of H. salinarum NRC-1 mismatch repair genes and phenotypic characterization of the mutants demonstrated that the mutS and mutL genes are not required for maintenance of the observed mutation rate. We established that H. salinarum NRC-1 mutS and mutL genes are redundant to an alternative system that limits spontaneous mutation in this organism. 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Mismatch repair is essential for retaining the fidelity of genetic information and defects in this pathway result in the deleterious accumulation of mutations and in hereditary diseases in humans. We calculated the spontaneous genomic mutation rate of H. salinarum NRC-1 using fluctuation tests targeting genes of the uracil monophosphate biosynthesis pathway. We found that H. salinarum NRC-1 has a low incidence of mutation suggesting the presence of active mechanisms to control spontaneous mutations during replication. The spectrum of mutational changes found in H. salinarum NRC-1, and in other archaea, appears to be unique to this domain of life and might be a consequence of their adaption to extreme environmental conditions. In-frame targeted gene deletions of H. salinarum NRC-1 mismatch repair genes and phenotypic characterization of the mutants demonstrated that the mutS and mutL genes are not required for maintenance of the observed mutation rate. 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We established that H. salinarum NRC-1 mutS and mutL genes are redundant to an alternative system that limits spontaneous mutation in this organism. This finding leads to the puzzling question of what mechanism is responsible for maintenance of the low genomic mutation rates observed in the Archaea, which for the most part do not have MutS and MutL homologs.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>20140215</pmid><doi>10.1371/journal.pone.0009045</doi><tpages>e9045</tpages><oa>free_for_read</oa></addata></record>
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subjects Active control
Adenosine Triphosphatases - genetics
Adenosine Triphosphatases - metabolism
Algorithms
Archaea
Archaeal Proteins - genetics
Archaeal Proteins - metabolism
Bacteria
Base Sequence
Biosynthesis
Cell Division - genetics
Deoxyribonucleic acid
DNA
DNA methylation
DNA polymerase
DNA repair
DNA Repair - genetics
DNA Repair Enzymes - genetics
DNA Repair Enzymes - metabolism
E coli
Environmental conditions
Escherichia coli
Eukarya
Genes
Genetic aspects
Genetics and Genomics
Genome, Archaeal
Genomes
Genomics
Halobacterium salinarum - genetics
Halobacterium salinarum - growth & development
Halobacterium salinarum - metabolism
Hereditary diseases
Homology
Ionizing radiation
Maintenance
Microbiology/Microbial Physiology and Metabolism
Microorganisms
Mismatch repair
Molecular Biology/DNA Repair
Mutants
Mutation
Mutation rates
MutS DNA Mismatch-Binding Protein - genetics
MutS DNA Mismatch-Binding Protein - metabolism
Physiological aspects
Proteins
Pyrimidines
Repair
Sequence Deletion
Studies
Trends
Uracil
Uridine Monophosphate - biosynthesis
title MutS and MutL are dispensable for maintenance of the genomic mutation rate in the halophilic archaeon Halobacterium salinarum NRC-1
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