Mechanism of Lagging-Strand DNA Replication in Eukaryotes

Adv Exp Med Biol. 2017:1042:117-133. doi: 10.1007/978-981-10-6955-0_6.

Abstract

This chapter focuses on the enzymes and mechanisms involved in lagging-strand DNA replication in eukaryotic cells. Recent structural and biochemical progress with DNA polymerase α-primase (Pol α) provides insights how each of the millions of Okazaki fragments in a mammalian cell is primed by the primase subunit and further extended by its polymerase subunit. Rapid kinetic studies of Okazaki fragment elongation by Pol δ illuminate events when the polymerase encounters the double-stranded RNA-DNA block of the preceding Okazaki fragment. This block acts as a progressive molecular break that provides both time and opportunity for the flap endonuclease 1 (FEN1) to access the nascent flap and cut it. The iterative action of Pol δ and FEN1 is coordinated by the replication clamp PCNA and produces a regulated degradation of the RNA primer, thereby preventing the formation of long-strand displacement flaps. Occasional long flaps are further processed by backup nucleases including Dna2.

Keywords: DNA polymerase α-primase; DNA polymerase δ; DNA replication; Dna2; Flap endonuclease 1; Lagging strand; Okazaki fragment maturation.

Publication types

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

MeSH terms

  • Animals
  • DNA / genetics*
  • DNA / metabolism*
  • DNA Polymerase I / metabolism
  • DNA Polymerase I / physiology
  • DNA Primase / metabolism
  • DNA Primase / physiology
  • DNA Primers / genetics
  • DNA Primers / metabolism
  • DNA Replication / physiology*
  • Eukaryota / genetics*
  • Eukaryotic Cells / metabolism*
  • Humans
  • Kinetics
  • RNA / metabolism

Substances

  • DNA Primers
  • Okazaki fragments
  • RNA
  • DNA
  • DNA Primase
  • DNA polymerase alpha-primase
  • DNA Polymerase I