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• W2021109997 endingPage "162" @default.
• W2021109997 startingPage "159" @default.
• W2021109997 abstract "Cytosine deamination to uracil occurs frequently in cellular DNA. In vitro, RNA polymerase efficiently inserts adenine opposite to uracil, resulting in G to A base substitutions. In vivo, uracil could potentially alter transcriptional fidelity, resulting in production of mutant proteins. This study demonstrates that in nondividing Escherichia coli cells, a DNA template base replaced with uracil in a stop codon in the firefly luciferase gene results in conversion of inactive to active luciferase. The level of transcriptional base substitution is dependent on the capacity to repair uracil. These results provide evidence for a DNA damage-dependent, transcription-driven pathway for generating mutant proteins in nondividing cells." @default.
• W2021109997 created "2016-06-24" @default.
• W2021109997 creator A5057550737 @default.
• W2021109997 creator A5061174828 @default.
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• W2021109997 date "1999-04-02" @default.
• W2021109997 modified "2023-10-14" @default.
• W2021109997 title "Phenotypic Change Caused by Transcriptional Bypass of Uracil in Nondividing Cells" @default.
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• W2021109997 doi "https://doi.org/10.1126/science.284.5411.159" @default.
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