cellular
• cre-treated mouse embryonic fibroblasts exposed to ionizing radiation exhibit a defect in the G2/M checkpoint compared to similarly treated heterozygous cells
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• cre-treated mouse embryonic fibroblasts exhibit increased cellular sensitivity to ionizing radiation compared to similarly treated heterozygous cells that is not as severe as in Lig4tm1Fwa cells
• cre-treated mouse embryonic fibroblasts exhibit defective DNA repair following treatment with ionizing radiation compared to in similarly treated heterozygous cells
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• cre-exposed mouse embryonic fibroblasts exhibit decreased growth rates by the second passage and no increase in numbers beyond passage three unlike similarly treated heterozygous cells
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• cre-treated mouse embryonic fibroblasts exhibit defective DNA repair following treatment with ionizing radiation compared to in similarly treated heterozygous cells
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• cre-exposed mouse embryonic fibroblasts (MEFs) exhibit chromosomal instability including chromosome or chromatid fragments, chromosome breaks or gaps in a single chromatid, occasional radial structures, and dicentrics unlike in similarly treated heterozygous cells
• MEFs exhibit more genomic instability compared to in Lig4tm1Fwa MEFs
• following exposure to gamma radiation, cre-exposed MEFs fail to exhibit a downward trend in frequency of chromosomal anomalies unlike similarly treated heterozygous cells
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• cre-treated mouse embryonic fibroblasts exhibit hypersensitivity to aphidicolin compared to similarly treated heterozygous cells
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homeostasis/metabolism
• cre-treated mouse embryonic fibroblasts exhibit defective DNA repair following treatment with ionizing radiation compared to in similarly treated heterozygous cells
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