[PDF][PDF] Localization of MCM2-7, Cdc45, and GINS to the site of DNA unwinding during eukaryotic DNA replication

M Pacek, AV Tutter, Y Kubota, H Takisawa, JC Walter - Molecular cell, 2006 - cell.com
M Pacek, AV Tutter, Y Kubota, H Takisawa, JC Walter
Molecular cell, 2006cell.com
Little is known about the architecture and biochemical composition of the eukaryotic DNA
replication fork. To study this problem, we used biotin-streptavidin-modified plasmids to
induce sequence-specific replication fork pausing in Xenopus egg extracts. Chromatin
immunoprecipitation was employed to identify factors associated with the paused fork. This
approach identifies DNA pol α, DNA pol δ, DNA pol ɛ, MCM2-7, Cdc45, GINS, and Mcm10
as components of the vertebrate replisome. In the presence of the DNA polymerase inhibitor …
Summary
Little is known about the architecture and biochemical composition of the eukaryotic DNA replication fork. To study this problem, we used biotin-streptavidin-modified plasmids to induce sequence-specific replication fork pausing in Xenopus egg extracts. Chromatin immunoprecipitation was employed to identify factors associated with the paused fork. This approach identifies DNA pol α, DNA pol δ, DNA pol ɛ, MCM2-7, Cdc45, GINS, and Mcm10 as components of the vertebrate replisome. In the presence of the DNA polymerase inhibitor aphidicolin, which causes uncoupling of a highly processive DNA helicase from the stalled replisome, only Cdc45, GINS, and MCM2-7 are enriched at the pause site. The data suggest the existence of a large molecular machine, the "unwindosome," which separates DNA strands at the replication fork and contains Cdc45, GINS, and the MCM2-7 holocomplex.
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