24 research outputs found
Direct observation of DNA threading in flap endonuclease complexes
Maintenance of genome integrity requires that branched nucleic acid molecules are
accurately processed to produce double-helical DNA. Flap endonucleases are essential
enzymes that trim such branched molecules generated by Okazaki fragment synthesis during
replication. Here, we report crystal structures of bacteriophage T5 flap endonuclease in
complexes with intact DNA substrates, and products, at resolutions of 1.9–2.2 Å. They reveal
single-stranded DNA threading through a hole in the enzyme enclosed by an inverted Vshaped
helical arch straddling the active site. Residues lining the hole induce an unusual
barb-like conformation in the DNA substrate juxtaposing the scissile phosphate and essential
catalytic metal ions. A series of complexes and biochemical analyses show how the
substrate’s single-stranded branch approaches, threads through, and finally emerges on the far
side of the enzyme. Our studies suggest that substrate recognition involves an unusual “flycasting,
thread, bend and barb” mechanis
Exploring patient-safety culture in the community pharmacy setting: a national cross-sectional study
Phosphate steering by Flap Endonuclease 1 promotes 5′-flap specificity and incision to prevent genome instability
DNA replication and repair enzyme Flap Endonuclease 1 (FEN1) is vital for genome integrity, and FEN1 mutations arise in multiple cancers. FEN1 precisely cleaves single-stranded (ss) 5'-flaps one nucleotide into duplex (ds) DNA. Yet, how FEN1 selects for but does not incise the ss 5'-flap was enigmatic. Here we combine crystallographic, biochemical and genetic analyses to show that two dsDNA binding sites set the 5'polarity and to reveal unexpected control of the DNA phosphodiester backbone by electrostatic interactions. Via 'phosphate steering', basic residues energetically steer an inverted ss 5'-flap through a gateway over FEN1's active site and shift dsDNA for catalysis. Mutations of these residues cause an 18,000-fold reduction in catalytic rate in vitro and large-scale trinucleotide (GAA)n repeat expansions in vivo, implying failed phosphate-steering promotes an unanticipated lagging-strand template-switch mechanism during replication. Thus, phosphate steering is an unappreciated FEN1 function that enforces 5'-flap specificity and catalysis, preventing genomic instability