Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2009-5-5
pubmed:abstractText
The premature human ageing Werner's syndrome is caused by loss or mutation of the WRN helicase/exonuclease. We have recently identified the orthologue of the WRN exonuclease in flies, DmWRNexo, encoded by the CG7670 locus, and showed very high levels of mitotic recombination in a hypomorphic PiggyBac insertional mutant. Here, we report a novel allele of CG7670, with a point mutation resulting in the change of the conserved aspartate (229) to valine. Flies bearing this mutation show levels of mitotic recombination 20-fold higher than wild type. Molecular modelling suggests that D229 lies towards the outside of the molecule distant from the nuclease active site. We have produced recombinant protein of the D229V mutant, assayed its nuclease activity in vitro, and compared activity with that of wild type DmWRNexo and a D162A E164A double active site mutant we have created. We show for the first time that DmWRNexo has 3'-5' exonuclease activity and that mutation within the presumptive active site disrupts exonuclease activity. Furthermore, we show that the D229V mutant has very limited exonuclease activity in vitro. Using Drosophila, we can therefore analyse WRN exonuclease from enzyme activity in vitro through to fly phenotype, and show that loss of exonuclease activity contributes to genome instability.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1389-5729
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
267-77
pubmed:meshHeading
pubmed-meshheading:18956248-Animals, pubmed-meshheading:18956248-Aspartic Acid, pubmed-meshheading:18956248-Catalytic Domain, pubmed-meshheading:18956248-Cloning, Molecular, pubmed-meshheading:18956248-DNA, Single-Stranded, pubmed-meshheading:18956248-Drosophila Proteins, pubmed-meshheading:18956248-Drosophila melanogaster, pubmed-meshheading:18956248-Exodeoxyribonucleases, pubmed-meshheading:18956248-Exonucleases, pubmed-meshheading:18956248-Genomic Instability, pubmed-meshheading:18956248-Genotype, pubmed-meshheading:18956248-Humans, pubmed-meshheading:18956248-Kinetics, pubmed-meshheading:18956248-Mitosis, pubmed-meshheading:18956248-Models, Molecular, pubmed-meshheading:18956248-Mutagenesis, Site-Directed, pubmed-meshheading:18956248-Phenotype, pubmed-meshheading:18956248-Point Mutation, pubmed-meshheading:18956248-Protein Conformation, pubmed-meshheading:18956248-RecQ Helicases, pubmed-meshheading:18956248-Recombinant Proteins, pubmed-meshheading:18956248-Recombination, Genetic, pubmed-meshheading:18956248-Temperature, pubmed-meshheading:18956248-Valine
pubmed:year
2009
pubmed:articleTitle
DmWRNexo is a 3'-5' exonuclease: phenotypic and biochemical characterization of mutants of the Drosophila orthologue of human WRN exonuclease.
pubmed:affiliation
Department of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't