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Updated: Aug 11, 2026

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
Published on: April 29, 2010
GINS, a central nexus in the archaeal DNA replication fork
Nina Marinsek1, Elizabeth R Barry, Kira S Makarova
1MRC Cancer Cell Unit, Hutchison MRC Research Centre, Hills Road, Cambridge CB2 2XZ, UK.
Archaeal GINS complex directly interacts with MCM helicase and primase, coordinating DNA replication fork architecture. This interaction couples leading-strand helicase progression with lagging-strand priming events.
Area of Science:
- Molecular Biology
- Biochemistry
- Genetics
Background:
- The GINS complex is crucial for eukaryotic DNA replication, particularly at the replication fork.
- It comprises four subunits: Psf1, Psf2, Psf3, and Sld5.
Purpose of the Study:
- To identify and characterize archaeal GINS complex homologues.
- To investigate the interaction of archaeal GINS with key DNA replication proteins like MCM helicase and primase.
Main Methods:
- Protein interaction studies.
- Identification of archaeal GINS complex subunits.
- Analysis of protein domains.
Main Results:
- An archaeal GINS homologue was identified as a direct interaction partner of the MCM helicase.
- The archaeal GINS complex consists of two poorly conserved eukaryotic GINS subunit homologues and a RecJ domain-containing protein.
- Archaeal GINS was shown to interact directly with the heterodimeric core primase.
Conclusions:
- Archaeal GINS plays a role in coordinating replication fork architecture.
- A mechanism is proposed where GINS couples MCM helicase progression on the leading strand with lagging-strand priming.
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