Early-onset lymphoma and extensive embryonic apoptosis in two domain-specific Fen1 mice mutants
Autor: | Christina Rada, Leonardo A. Meza-Zepeda, Gaute Nesse, Jon K. Laerdahl, Liv Kleppa, Arne Klungland, Richard W. Doughty, Cesilie G. Castellanos, Michael S. Neuberger, Trine J. Meza, Elisabeth Larsen, Guro Flor Lien |
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Rok vydání: | 2008 |
Předmět: |
DNA Replication
Male Cancer Research DNA Repair Lymphoma DNA repair Flap Endonucleases DNA polymerase II Flap structure-specific endonuclease 1 Eukaryotic DNA replication Apoptosis DNA polymerase delta Culture Media Serum-Free Mice Proliferating Cell Nuclear Antigen Animals Obesity Cells Cultured Cell Proliferation Recombination Genetic Okazaki fragments biology Genes Immunoglobulin Point mutation Cell Cycle Nucleic Acid Hybridization Embryo Mammalian Molecular biology Mice Mutant Strains Proliferating cell nuclear antigen Protein Structure Tertiary Oncology Animals Newborn Mutation biology.protein Female Genes Lethal Insulin Resistance |
Zdroj: | Cancer research. 68(12) |
ISSN: | 1538-7445 |
Popis: | Flap endonuclease 1 (FEN1) processes Okazaki fragments in lagging strand DNA synthesis, and FEN1 is involved in several DNA repair pathways. The interaction of FEN1 with the proliferating cell nuclear antigen (PCNA) processivity factor is central to the function of FEN1 in both DNA replication and repair. Here we present two gene-targeted mice with mutations in FEN1. The first mutant mouse carries a single amino acid point mutation in the active site of the nuclease domain of FEN1 (Fen1E160D/E160D), and the second mutant mouse contains two amino acid substitutions in the highly conserved PCNA interaction domain of FEN1 (Fen1ΔPCNA/ΔPCNA). Fen1E160D/E160D mice develop a considerably elevated incidence of B-cell lymphomas beginning at 6 months of age, particularly in females. By 16 months of age, more than 90% of the Fen1E160D/E160D females have tumors, primarily lymphomas. By contrast, Fen1ΔPCNA/ΔPCNA mouse embryos show extensive apoptosis in the forebrain and vertebrae area and die around stage E9.5 to E11.5. [Cancer Res 2008;68(12):4571–8] |
Databáze: | OpenAIRE |
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