Ctf4/AND-1 is a highly conserved gene product required for both DNA replication and the establishment of sister chromatid cohesion. In this report, we examined the mechanism of action of human Ctf4 (hCtf4) in DNA replication both in vitro and in vivo. Our findings show that the purified hCtf4 exists as a dimer and that the hCtf4 SepB domain likely plays a primary role determining the dimeric structure. hCtf4 binds preferentially to DNA template-primer structures, interacts directly with the replicative DNA polymerases (α, δ, and ε), and markedly stimulates the polymerase activities of DNA polymerases α and ε in vitro. Depletion of hCtf4 in HeLa cells by small interfering RNA resulted in G1/S phase arrest. DNA fiber analysis revealed that cells depleted of hCtf4 exhibited a rate of DNA replication slower than cells treated with control small interfering RNA. These findings suggest that in human cells, hCtf4 plays an essential role in DNA replication and its ability to stimulate the replicative DNA polymerases may contribute to this effect. © 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
CITATION STYLE
Bermudez, V. P., Farina, A., Tappin, I., & Hurwitz, J. (2010). Influence of the human cohesion establishment factor Ctf4/AND-1 on DNA replication. Journal of Biological Chemistry, 285(13), 9493–9505. https://doi.org/10.1074/jbc.M109.093609
Mendeley helps you to discover research relevant for your work.