» Articles » PMID: 32341532

Rad53 Limits CMG Helicase Uncoupling from DNA Synthesis at Replication Forks

Overview
Date 2020 Apr 29
PMID 32341532
Citations 32
Authors
Affiliations
Soon will be listed here.
Abstract

The coordination of DNA unwinding and synthesis at replication forks promotes efficient and faithful replication of chromosomal DNA. Disruption of the balance between helicase and polymerase activities during replication stress leads to fork progression defects and activation of the Rad53 checkpoint kinase, which is essential for the functional maintenance of stalled replication forks. The mechanism of Rad53-dependent fork stabilization is not known. Using reconstituted budding yeast replisomes, we show that mutational inactivation of the leading strand DNA polymerase, Pol ε, dNTP depletion, and chemical inhibition of DNA polymerases cause excessive DNA unwinding by the replicative DNA helicase, CMG, demonstrating that budding yeast replisomes lack intrinsic mechanisms that control helicase-polymerase coupling at the fork. Importantly, we find that the Rad53 kinase restricts excessive DNA unwinding at replication forks by limiting CMG helicase activity, suggesting a mechanism for fork stabilization by the replication checkpoint.

Citing Articles

Competition for the nascent leading strand shapes the requirements for PCNA loading in the replisome.

Fletcher E, Jones M, Yeeles J EMBO J. 2025; .

PMID: 40021844 DOI: 10.1038/s44318-025-00386-4.


A tale of two strands: Decoding chromatin replication through strand-specific sequencing.

Li Z, Zhang Z Mol Cell. 2025; 85(2):238-261.

PMID: 39824166 PMC: 11750172. DOI: 10.1016/j.molcel.2024.10.035.


Stabilization of expandable DNA repeats by the replication factor Mcm10 promotes cell viability.

Masnovo C, Paleiov Z, Dovrat D, Baxter L, Movafaghi S, Aharoni A Nat Commun. 2024; 15(1):10532.

PMID: 39627228 PMC: 11615337. DOI: 10.1038/s41467-024-54977-6.


The fork protection complex generates DNA topological stress-induced DNA damage while ensuring full and faithful genome duplication.

Keszthelyi A, Mansoubi S, Whale A, Houseley J, Baxter J Proc Natl Acad Sci U S A. 2024; 121(49):e2413631121.

PMID: 39589889 PMC: 11626154. DOI: 10.1073/pnas.2413631121.


Revised mechanism of hydroxyurea-induced cell cycle arrest and an improved alternative.

Shaw A, Mihelich M, Whitted J, Reitman H, Timmerman A, Tehseen M Proc Natl Acad Sci U S A. 2024; 121(42):e2404470121.

PMID: 39374399 PMC: 11494364. DOI: 10.1073/pnas.2404470121.


References
1.
Kim S, Dallmann H, McHenry C, Marians K . Coupling of a replicative polymerase and helicase: a tau-DnaB interaction mediates rapid replication fork movement. Cell. 1996; 84(4):643-50. DOI: 10.1016/s0092-8674(00)81039-9. View

2.
Manosas M, Spiering M, Ding F, Croquette V, Benkovic S . Collaborative coupling between polymerase and helicase for leading-strand synthesis. Nucleic Acids Res. 2012; 40(13):6187-98. PMC: 3401439. DOI: 10.1093/nar/gks254. View

3.
Stano N, Jeong Y, Donmez I, Tummalapalli P, Levin M, Patel S . DNA synthesis provides the driving force to accelerate DNA unwinding by a helicase. Nature. 2005; 435(7040):370-3. PMC: 1563444. DOI: 10.1038/nature03615. View

4.
Yeeles J, Janska A, Early A, Diffley J . How the Eukaryotic Replisome Achieves Rapid and Efficient DNA Replication. Mol Cell. 2016; 65(1):105-116. PMC: 5222725. DOI: 10.1016/j.molcel.2016.11.017. View

5.
Georgescu R, Langston L, Yao N, Yurieva O, Zhang D, Finkelstein J . Mechanism of asymmetric polymerase assembly at the eukaryotic replication fork. Nat Struct Mol Biol. 2014; 21(8):664-70. PMC: 4482249. DOI: 10.1038/nsmb.2851. View