Arranging eukaryotic nuclear DNA polymerases for replication: Specific interactions with accessory proteins arrange Pols α, δ, and ϵ in the replisome for leading-strand and lagging-strand DNA replication

Bioessays. 2017 Aug;39(8):10.1002/bies.201700070. doi: 10.1002/bies.201700070.

Abstract

Biochemical and cryo-electron microscopy studies have just been published revealing interactions among proteins of the yeast replisome that are important for highly coordinated synthesis of the two DNA strands of the nuclear genome. These studies reveal key interactions important for arranging DNA polymerases α, δ, and ϵ for leading and lagging strand replication. The CMG (Mcm2-7, Cdc45, GINS) helicase is central to this interaction network. These are but the latest examples of elegant studies performed in the recent past that lead to a much better understanding of how the eukaryotic replication fork achieves efficient DNA replication that is accurate enough to prevent diseases yet allows evolution.

Keywords: DNA polymerases; DNA replication; cryo-electron microscopy; initiation of replication; replisome.

Publication types

  • Review

MeSH terms

  • Cryoelectron Microscopy
  • DNA Helicases / genetics
  • DNA Helicases / metabolism
  • DNA Replication / genetics
  • DNA Replication / physiology
  • DNA-Directed DNA Polymerase / genetics
  • DNA-Directed DNA Polymerase / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism

Substances

  • Saccharomyces cerevisiae Proteins
  • DNA-Directed DNA Polymerase
  • DNA Helicases