Ontology highlight
ABSTRACT:
SUBMITTER: Bermudez VP
PROVIDER: S-EPMC2843200 | biostudies-literature | 2010 Mar
REPOSITORIES: biostudies-literature
The Journal of biological chemistry 20100119 13
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 repl ...[more]