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Fork sensing and strand switching control antagonistic activities of RecQ helicases

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TLDR
This work investigates the DNA unwinding of RecQ helicases from Arabidopsis thaliana, AtRECQ2 and AtRECZ3 at the single-molecule level using magnetic tweezers and provides a simple explanation for how different biological activities can be achieved by rather similar members of the RecQ family.
Abstract
RecQ helicases have essential roles in maintaining genome stability during replication and in controlling double-strand break repair by homologous recombination. Little is known about how the different RecQ helicases found in higher eukaryotes achieve their specialized and partially opposing functions. Here, we investigate the DNA unwinding of RecQ helicases from Arabidopsis thaliana, AtRECQ2 and AtRECQ3 at the single-molecule level using magnetic tweezers. Although AtRECQ2 predominantly unwinds forked DNA substrates in a highly repetitive fashion, AtRECQ3 prefers to rewind, that is, to close preopened DNA forks. For both enzymes, this process is controlled by frequent strand switches and active sensing of the unwinding fork. The relative extent of the strand switches towards unwinding or towards rewinding determines the predominant direction of the enzyme. Our results provide a simple explanation for how different biological activities can be achieved by rather similar members of the RecQ family.

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Journal ArticleDOI

Camera-based three-dimensional real-time particle tracking at kHz rates and Ångström accuracy

TL;DR: This work demonstrates that camera-based imaging can provide a similar performance for all three dimensions of particle tracking with Ångström accuracy as laser detection through photodiodes, and provides a simple and robust way for high-resolution tweezers experiments using multiple particles at a time.
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Mechanistic insight into the interaction of BLM helicase with intra-strand G-quadruplex structures.

TL;DR: It is shown that the activity of BLM is substrate dependent, and highly regulated by a short ssDNA segment that separates the G4 motif from dsDNA, and a model is presented that proposes a unique role for G4 structures in modulating theActivity of DNA processing enzymes.
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Human DNA2 possesses a cryptic DNA unwinding activity that functionally integrates with BLM or WRN helicases

TL;DR: It is shown that the helicase of hDNA2 functionally integrates with BLM or WRN helicases to promote dsDNA degradation by forming a heterodimeric molecular machine, which collectively suggests that the h DNA2 motor promotes the enzyme's capacity to degrade ds DNA in conjunction with BLMor WRN and thus promote the repair of broken DNA.
Journal ArticleDOI

Dynamic look at DNA unwinding by a replicative helicase

TL;DR: The findings reveal that E1 employs a strand exclusion mechanism to unwind DNA with the N-terminal side leading at the replication fork, and DNA unwinding by E1 is modulated by the origin-recognition domain, suggesting a previously unsuspected role for this domain in regulating helicase activity.
Journal ArticleDOI

Extending the Range for Force Calibration in Magnetic Tweezers

TL;DR: The force calibration based on the long pendulum geometry will facilitate high-resolution magnetic-tweezers experiments that rely on short molecules and large forces, as well as highly parallelized measurements that use low frame rates.
References
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Journal ArticleDOI

SSB protein diffusion on single-stranded DNA stimulates RecA filament formation

TL;DR: It is shown, using single-molecule two- and three-colour fluorescence resonance energy transfer, that tetrameric SSB can spontaneously migrate along ssDNA, a new model for how an SSB protein can be redistributed, while remaining tightly bound to ssDNA during recombination and repair processes.
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Single-Molecule Studies Reveal Dynamics of DNA Unwinding by the Ring-Shaped T7 Helicase

TL;DR: In insights into possible ways helicase activity is enhanced by associated proteins, an active unwinding model fully supports the data even though the helicase on its own does not unwind at its optimal rate.
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Single-molecule assay reveals strand switching and enhanced processivity of UvrD

TL;DR: A single-molecule manipulation technique is used to monitor real-time changes in extension of a single, stretched, nicked dsDNA substrate as it is unwound by a single enzyme, and observes a feature not seen in bulk assays: unwinding is preferentially followed by a slow, enzyme-translocation-limited rezipping of the separated strands.
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PcrA Helicase Dismantles RecA Filaments by Reeling in DNA in Uniform Steps

TL;DR: It is discovered that PcrA preferentially translocates on the DNA lagging strand instead of unwinding the template duplex, suggesting a mode of action for eliminating potentially deleterious recombination intermediates.
Journal ArticleDOI

Two closely related RecQ helicases have antagonistic roles in homologous recombination and DNA repair in Arabidopsis thaliana

TL;DR: It is suggested that in plants RECQ4A is functionally equivalent to SGS1 of Saccharomyces cerevisiae and the mammalian BLM protein, and mutants of the closely related RECZ4B are not mutagen-sensitive, not viable in a mus81 background, and unable to suppress the induced lethality caused by loss of TOP3α.
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