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A four-point molecular handover during Okazaki maturation
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Abstract
DNA replication introduces thousands of RNA primers into the lagging strand that need to be removed for replication to be completed. In Escherichia coli when the replicative DNA polymerase Pol IIIα terminates at a previously synthesized RNA primer, DNA Pol I takes over and continues DNA synthesis while displacing the downstream RNA primer. The displaced primer is subsequently excised by an endonuclease, followed by the sealing of the nick by a DNA ligase. Yet how the sequential actions of Pol IIIα, Pol I polymerase, Pol I endonuclease and DNA ligase are coordinated is poorly defined. Here we show that each enzymatic activity prepares the DNA substrate for the next activity, creating an efficient four-point molecular handover. The cryogenic-electron microscopy structure of Pol I bound to a DNA substrate with both an upstream and downstream primer reveals how it displaces the primer in a manner analogous to the monomeric helicases. Moreover, we find that in addition to its flap-directed nuclease activity, the endonuclease domain of Pol I also specifically cuts at the RNA-DNA junction, thus marking the end of the RNA primer and creating a 5' end that is a suitable substrate for the ligase activity of LigA once all RNA has been removed.
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Idling by DNA polymerase δ maintains a ligatable nick during lagging-strand DNA replication
Garg, P., Stith, C. M., Sabouri, N., Johansson, E., & Burgers, P. M. (2004) · Genes & Development · doi:10.1101/gad.1252304 · Cited by 211
Rychlik, M. P., Chon, H., Cerritelli, S. M., Klimek, P., Crouch, R. J., & Nowotny, M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.11.001 · Cited by 109
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Metadata
- Authors
- Botto, M. M., Borsellini, A., & Lamers, M. H.
- Affiliations
- University of Geneva (CH)
- Leiden University Medical Center (NL)
- Corresponding author
- Lamers, Meindert H.
- Venue
- Nature Structural & Molecular Biology
- Published
- 2023-08-24
- Volume
- 30
- Issue
- 10
- Pages
- 1505-1515
- ISSN
- 1545-9985 (ISSN-L)
- 1545-9993
- OpenAlex
- W4386142497
- Cited by
- 9
- References
- 3
- Citations by year
- 2026: 5 · 2025: 3 · 2024: 1
- FWCI
- 0.80
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Licence
- Locations
- Nature Structural & Molecular Biology (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Leiden Repository (Leiden University) (submittedVersion)
- Funders
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (184.034.014)
- Leids Universitair Medisch Centrum
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- Okazaki fragment maturation, RNA primer removal, DNA polymerase I, lagging strand synthesis, Escherichia coli DNA replication, flap endonuclease, cryo-EM structure
- MeSH terms
- DNA Ligase ATP, DNA, DNA Polymerase III, DNA Replication, Endonucleases, DNA Ligases, RNA
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