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Updated: Aug 13, 2026

Production of Double-stranded DNA Ministrings
Published on: February 29, 2016
Essential elements of a licensed, mammalian plasmid origin of DNA synthesis
Jindong Wang1, Scott E Lindner, Elizabeth R Leight
1McArdle Laboratory for Cancer Research, University of Wisconsin--Madison, Madison, WI 53706, USA.
Abstract:
We developed a mammalian plasmid replicon with a formerly uncharacterized origin of DNA synthesis, 8xRep*. 8xRep* functions efficiently to support once-per-cell-cycle synthesis of plasmid DNA which initiates within Rep*. By characterizing Rep*'s requirements for acting as an origin, we have uncovered several striking properties it shares with DS, the only other well-characterized, licensed, mammalian plasmid origin of DNA synthesis. Rep* contains a pair of previously unrecognized Epstein-Barr nuclear antigen 1 (EBNA1)-binding sites that are both necessary and sufficient in cis for its origin activity. These sites have an essential 21-bp center-to-center spacing, are bent by EBNA1, and recruit the origin recognition complex. The properties shared between DS and Rep* define cis and trans characteristics of a mammalian, extrachromosomal replicon. The role of EBNA1 likely reflects its evolution from cellular factors involved in the assembly of the initiation machinery.
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