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Autocatalytic selection improves gene functions in vitro, suggesting progress towards synthetic cell construction.
The integration of biological functions into a single operating system is considered a major challenge in the construction of a synthetic cell 1-3 . We present autocatalytic selection (ACS) of gene functions as a driver for integrating biological modules in vitro. A gene of interest (GOI) is introduced into a minimal DNA self-replicator based on the φ29 replication machinery 4 and the function of the GOI is linked to transcription, translation or DNA replication through a positive feedback loop. As the encoded function eventually promotes DNA self-replication, the gene variants with greater activity are selected. Using different coupling mechanisms, we demonstrate ACS of three functions: transcription, synthesis of a deoxynucleoside triphosphate for DNA replication, and β-galactosidase activity. The latter example illustrates how a function that is unrelated to the Central Dogma can be selected. This work paves the way for ACS-driven Darwinian evolution of virtually any biomolecule in vitro, streamlining the construction of increasingly complex synthetic cells as well as the engineering of biotechnologically relevant enzymes.
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Danelon et al. (2025) studied this question.
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