Biochemical analyses indicate that binding and cleavage specificities define the ordered processing of human Okazaki fragments by Dna2 and FEN1

In eukaryotic Okazaki fragment processing, the RNA primer is displaced into a single-stranded FLAP prior to removal. Evidence suggests that some flaps become long before they are cleaved, and that this cleavage involves the sequential action of two nucleases. Strand displacement characteristics of the polymerase show that a short gap precedes the FLAP during synthesis. Using biochemical techniques, binding and cleavage assays presented here indicate that when the FLAP is ∼ 30 nt long the nuclease Dna2 can bind with high affinity to the FLAP and downstream double strand and begin cleavage. When the polymerase idles or dissociates the Dna2 can reorient for additional contacts with the upstream primer region, allowing the nuclease to remain stably bound as the FLAP is further shortened. The DNA can then equilibrate to a double FLAP that can bind Dna2 and FLAP endonuclease (FEN1) simultaneously. When Dna2 shortens the FLAP even more, FEN1 can displace the Dna2 and cleave at the FLAP base to make a nick for ligation.