Plasmid copy number is presented as a gene-dosage variable that shapes phenotypic mutation rate in engineered genetic modules. The abstract states that higher PCN facilitates emergence of gain-of-function mutations while curbing spread of loss-of-function mutations.
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plasmid copy number
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PCN
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Greater plasmid copy number curbs the spread of loss-of-function mutations.
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it instead curbs the spread of loss-of-function mutations
Greater plasmid copy number facilitates the emergence of gain-of-function mutations.
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while greater PCN facilitates the emergence of gain-of-function mutations
Plasmid copy number and regulatory architecture jointly affect phenotypic mutation rate in engineered genetic modules.
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we characterize how the interplay of gene dosage via plasmid copy number (PCN) and regulatory architecture affect the phenotypic mutation rate
Regulatory-region mutations become more phenotypically prominent as plasmid copy number increases, including under constitutive regulator expression and self-repression.
Quoted textsource-backed
those occurring in the regulatory region which become more prominent as PCN increases, both when the regulator is expressed constitutively and when it is self-repressed