Essential elements of a licensed, mammalian plasmid origin of DNA synthesis

Mol Cell Biol. 2006 Feb;26(3):1124-34. doi: 10.1128/MCB.26.3.1124-1134.2006.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Binding Sites
  • Cells, Cultured
  • DNA Replication*
  • Epstein-Barr Virus Nuclear Antigens / metabolism*
  • Humans
  • Molecular Sequence Data
  • Plasmids / genetics
  • Plasmids / metabolism*
  • Replication Origin*

Substances

  • Epstein-Barr Virus Nuclear Antigens