Literature DB >> 16783005

The relative roles of three DNA repair pathways in preventing Caenorhabditis elegans mutation accumulation.

Dee R Denver1, Seth Feinberg, Catherine Steding, Matthew D Durbin, Michael Lynch.   

Abstract

Mutation is a central biological process whose rates and spectra are influenced by a variety of complex and interacting forces. Although DNA repair pathways are generally known to play key roles in maintaining genetic stability, much remains to be understood about the relative roles of different pathways in preventing the accumulation of mutations and the extent of heterogeneity in pathway-specific repair efficiencies across different genomic regions. In this study we examine mutation processes in base excision repair-deficient (nth-1) and nucleotide excision repair-deficient (xpa-1) Caenorhabditis elegans mutation-accumulation (MA) lines across 24 regions of the genome and compare our observations to previous data from mismatch repair-deficient (msh-2 and msh-6) and wild-type (N2) MA lines. Drastic variation in both average and locus-specific mutation rates, ranging two orders of magnitude for the latter, was detected among the four sets of repair-deficient MA lines. Our work provides critical insights into the relative roles of three DNA repair pathways in preventing C. elegans mutation accumulation and provides evidence for the presence of pathway-specific DNA repair territories in the C. elegans genome.

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Year:  2006        PMID: 16783005      PMCID: PMC1569771          DOI: 10.1534/genetics.106.059840

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  38 in total

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6.  The fitness effects of spontaneous mutations in Caenorhabditis elegans.

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7.  Mutation rates, spectra and hotspots in mismatch repair-deficient Caenorhabditis elegans.

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9.  Synergism between base excision repair, mediated by the DNA glycosylases Ntg1 and Ntg2, and nucleotide excision repair in the removal of oxidatively damaged DNA bases in Saccharomyces cerevisiae.

Authors:  L Gellon; R Barbey; P Auffret van der Kemp; D Thomas; S Boiteux
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Review 10.  Oxidative base damage to DNA: specificity of base excision repair enzymes.

Authors:  J Cadet; A G Bourdat; C D'Ham; V Duarte; D Gasparutto; A Romieu; J L Ravanat
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  22 in total

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Review 3.  C. elegans as an Animal Model to Study the Intersection of DNA Repair, Aging and Neurodegeneration.

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4.  A two-tiered compensatory response to loss of DNA repair modulates aging and stress response pathways.

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Journal:  Aging (Albany NY)       Date:  2010-03-31       Impact factor: 5.682

5.  Nucleotide excision repair genes are expressed at low levels and are not detectably inducible in Caenorhabditis elegans somatic tissues, but their function is required for normal adult life after UVC exposure.

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6.  Replication blocking lesions present a unique substrate for homologous recombination.

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7.  In vivo repair of alkylating and oxidative DNA damage in the mitochondrial and nuclear genomes of wild-type and glycosylase-deficient Caenorhabditis elegans.

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8.  Evolution of a higher intracellular oxidizing environment in Caenorhabditis elegans under relaxed selection.

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9.  A systems approach defining constraints of the genome architecture on lineage selection and evolvability during somatic cancer evolution.

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Review 10.  Caenorhabditis elegans: an emerging model in biomedical and environmental toxicology.

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