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Updated: Jul 30, 2026

Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
Published on: October 9, 2009
Conjugative DNA synthesis: R1162 and the question of rolling-circle replication
Christopher Parker1, Xiao-lin Zhang, Dorian Henderson
1Section of Molecular Genetics and Microbiology, School of Biology, University of Texas at Austin, Austin, TX 78712, USA.
Abstract:
Strand-replacement synthesis during conjugative mating has been characterized by introducing into donor cells R1162 plasmid DNA containing a base-pair mismatch. Conjugative synthesis in donors occurs in the absence of vegetative plasmid replication, but with a lag between rounds of transfer, and with most strands being initiated at the normal site within the replicative origin. These characteristics argue against the idea that multiple plasmid copies are generated for successive rounds of transfer by rolling-circle replication. However, the R1162 relaxase protein can process molecules containing multiple transfer origins in the manner expected for the conversion of single-strand multimers, generated by rolling-circle replication, to unit-length molecules. This capability appears to be the result of a secondary cleavage reaction carried out by the protein. The possibility is raised that the processing of molecules with more than one origin of transfer might be a repair mechanism directed against adventitious DNA synthesis during transfer.
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