scispace - formally typeset
Open AccessJournal ArticleDOI

Fork sensing and strand switching control antagonistic activities of RecQ helicases

Reads0
Chats0
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.

read more

Content maybe subject to copyright    Report

Citations
More filters
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.
Journal ArticleDOI

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.
Journal ArticleDOI

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
More filters
Journal ArticleDOI

5'-Single-stranded/duplex DNA junctions are loading sites for E. coli UvrD translocase.

TL;DR: This work shows that a monomer also binds with specificity to DNA junctions possessing a 5′‐ssDNA flanking region and can initiate translocation from this site, and suggests that amonomeric UvrD translocase can be loaded at a 5‐ss DNA junction when translocation activity alone is needed.
Journal ArticleDOI

Nicking enzyme–based internal labeling of DNA at multiple loci

TL;DR: It is shown that modifications can be introduced at distant loci within one molecule in a simple one-pot reaction and achieved labeling on both strands at a specific locus, as demonstrated by Förster resonance energy transfer (FRET) experiments.
Journal ArticleDOI

AtRECQ2, a RecQ helicase homologue from Arabidopsis thaliana, is able to disrupt various recombinogenic DNA structures in vitro.

TL;DR: The biochemical properties defined in this work support the hypothesis that AtRECQ2 might be functionally orthologous to the helicase part of the human RecQ homologue HsWRN.
Journal ArticleDOI

Scanning evanescent fields using a pointlike light source and a nanomechanical DNA gear.

TL;DR: This work uses a four-arm DNA junction as a nanomechanical translation stage to move a single fluorescent quantum dot through an exponentially decaying evanescent field to allow the characterization of a broad range of illumination fields and to study near-field effects between small optical probes.
Journal ArticleDOI

Complex activities of the human Bloom's syndrome helicase are encoded in a core region comprising the RecA and Zn-binding domains

TL;DR: A quantitative mechanistic analysis of truncated BLM constructs that are shorter than the previously identified minimal functional module found that a BLM construct comprising only the two conserved RecA domains and the Zn2+-binding domain can efficiently perform all mentioned HR-related activities.
Related Papers (5)