Evidence map›Paper›PMID 37409572›Full record

ArticleNucleic acids research2023

Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing.

Rebecca J Lever, Emily Simmons, Rebecca Gamble-Milner, Ryan J Buckley, Catherine Harrison, Ashley J Parkes, Laura Mitchell, Jacob A Gausden, Sanja Škulj, Branimir Bertoša and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Helicase HELQ: Molecular Characters Fit for DSB Repair Function.International journal of molecular sciences · 2024
    Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Rebecca J LeverSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Emily SimmonsSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Rebecca Gamble-MilnerSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Ryan J BuckleySchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Catherine HarrisonSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Ashley J ParkesSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Laura MitchellSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Jacob A GausdenSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.
Sanja ŠkuljDepartment of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, HR-10000 Zagreb, Croatia.
Branimir BertošaDepartment of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, HR-10000 Zagreb, Croatia.
Edward L BoltSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.ORCID 0000-0002-5656-7706
Thorsten AllersSchool of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.ORCID 0000-0002-7308-3332
University of Nottingham · GBUniversity of Zagreb · HR

Funding

Biotechnology and Biological Sciences Research Council BB/M008770/1Biotechnology and Biological Sciences Research Council BB/R007543/1Biotechnology and Biological Sciences Research Council BB/T006625/1
6 · The paper itself

Abstract

Hel308 helicases promote genome stability in archaea and are conserved in metazoans, where they are known as HELQ. Their helicase mechanism is well characterised, but it is unclear how they specifically contribute to genome stability in archaea. We show here that a highly conserved motif of Hel308/HELQ helicases (motif IVa, F/YHHAGL) modulates both DNA unwinding and a newly identified strand annealing function of archaeal Hel308. A single amino acid substitution in motif IVa results in hyper-active DNA helicase and annealase activities of purified Hel308 in vitro. All-atom molecular dynamics simulations using Hel308 crystal structures provided a molecular basis for these differences between mutant and wild type Hel308. In archaeal cells, the same mutation results in 160000-fold increased recombination, exclusively as gene conversion (non-crossover) events. However, crossover recombination is unaffected by the motif IVa mutation, as is cell viability or DNA damage sensitivity. By contrast, cells lacking Hel308 show impaired growth, increased sensitivity to DNA cross-linking agents, and only moderately increased recombination. Our data reveal that archaeal Hel308 suppresses recombination and promotes DNA repair, and that motif IVa in the RecA2 domain acts as a catalytic switch to modulate the separable recombination and repair activities of Hel308.

Indexed as

ArchaeaDNA HelicasesDNADNA RepairGenomic InstabilityHumansRecombination, GeneticDNADNA Helicases

Identifiers

PMID37409572
PMCPMC10484726
OpenAlexW4383301537

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.