CMG helicase and DNA polymerase ε form a functional 15-subunit holoenzyme for eukaryotic leading-strand DNA replication
CMG helicase and DNA polymerase ε form a functional 15-subunit holoenzyme for eukaryotic leading-strand DNA replication
Significance All cells must replicate their chromosomes prior to cell division. This process is carried out by a collection of proteins, known as the replisome, that act together to unwind the double helix and synthesize two new DNA strands complementary to the two parental strands. The details of replisome function have been worked out for bacteria but are much less well understood for eukaryotic cells. We have developed a system for studying eukaryotic replisome function in vitro using purified proteins. Using this system, we have identified a direct interaction between the component that unwinds the DNA, the CMG (Cdc45-MCM-GINS) helicase, and the component that replicates the leading strand, DNA polymerase ε, to form a large helicase–polymerase holoenzyme comprising 15 separate proteins.
- University of Chicago United States
- Howard Hughes Medical Institute United States
- Rockefeller University United States
DNA Replication, Saccharomyces cerevisiae Proteins, Time Factors, DNA Helicases, DNA Polymerase II, Saccharomyces cerevisiae, Models, Biological, Substrate Specificity, Protein Subunits, Chromatography, Gel, DNA, Circular, Holoenzymes
DNA Replication, Saccharomyces cerevisiae Proteins, Time Factors, DNA Helicases, DNA Polymerase II, Saccharomyces cerevisiae, Models, Biological, Substrate Specificity, Protein Subunits, Chromatography, Gel, DNA, Circular, Holoenzymes
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