TY - JOUR
T1 - Polymerase dynamics at the eukaryotic DNA replication fork
AU - Burgers, Peter M.J.
PY - 2009/2/13
Y1 - 2009/2/13
N2 - This review discusses recent insights in the roles of DNA polymerases (Pol) δ and ε in eukaryotic DNA replication. A growing body of evidence specifies Pol ε as the leading strand DNA polymerase and Pol δ as the lagging strand polymerase during undisturbed DNA replication. New evidence supporting this model comes from the use of polymerase mutants that show an asymmetric mutator phenotype for certain mispairs, allowing an unambiguous strand assignment for these enzymes. On the lagging strand, Pol δ corrects errors made by Pol α during Okazaki fragment initiation. During Okazaki fragment maturation, the extent of strand displacement synthesis by Pol δ determines whether maturation proceeds by the short or long flap processing pathway. In the more common short flap pathway, Pol δ coordinates with the flap endonuclease FEN1 to degrade initiator RNA, whereas in the long flap pathway, RNA removal is initiated by the Dna2 nuclease/ helicase.
AB - This review discusses recent insights in the roles of DNA polymerases (Pol) δ and ε in eukaryotic DNA replication. A growing body of evidence specifies Pol ε as the leading strand DNA polymerase and Pol δ as the lagging strand polymerase during undisturbed DNA replication. New evidence supporting this model comes from the use of polymerase mutants that show an asymmetric mutator phenotype for certain mispairs, allowing an unambiguous strand assignment for these enzymes. On the lagging strand, Pol δ corrects errors made by Pol α during Okazaki fragment initiation. During Okazaki fragment maturation, the extent of strand displacement synthesis by Pol δ determines whether maturation proceeds by the short or long flap processing pathway. In the more common short flap pathway, Pol δ coordinates with the flap endonuclease FEN1 to degrade initiator RNA, whereas in the long flap pathway, RNA removal is initiated by the Dna2 nuclease/ helicase.
UR - http://www.scopus.com/inward/record.url?scp=63249130106&partnerID=8YFLogxK
U2 - 10.1074/jbc.R800062200
DO - 10.1074/jbc.R800062200
M3 - Short survey
C2 - 18835809
AN - SCOPUS:63249130106
SN - 0021-9258
VL - 284
SP - 4041
EP - 4045
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 7
ER -