PubMed · 1998 · 157 citations · 25 references
Life SciencesGeneticsMolecular GeneticsCancer GeneticsDna RepairMolecular OncologyCancer GenomicsDna Double-strand Break RepairHereditary Cancer SyndromesHomologous RecombinationMismatch RepairRecombination ProteinsCancer Susceptibility SyndromesDna In Situ HybridizationExonuclease 1Inherited Cancer SusceptibilityMismatch Repair PathwayMutator AllelesMutator PhenotypesRadiation Hybrid Mapping
DNA mismatch repair (MMR) plays a vital role in the faithful replication of DNA, and its inactivation leads to a mutator phenotype that has been associated with the common cancer susceptibility syndrome Hereditary Non-Polyposis Colorectal Cancer (HNPCC). Here, we report on a novel human exonuclease (hExoI) that is related to the yeast exonuclease 1. The hExoI cDNA comprises 2541 bp, which code for a Mr 94,000 protein that appears to be highly expressed in testis tissue and at very low levels in other tissues. The hExoI gene has 14 exons and is located on chromosome 1q43, as determined by fluorescence in situ hybridization and radiation hybrid mapping. hExoI was found to interact strongly with the human MMR protein hMSH2, suggesting its involvement in the MMR process and/or DNA recombination.
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CpG Islands in vertebrate genomes
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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
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Mutator phenotype may be required for multistage carcinogenesis.