Evidence map›Paper›PMID 25722374›Full record

ArticleNucleic acids research2015

Dynamic Escherichia coli SeqA complexes organize the newly replicated DNA at a considerable distance from the replisome.

Emily Helgesen, Solveig Fossum-Raunehaug, Frank Sætre, Kay Oliver Schink, Kirsten Skarstad

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  4. Compaction and Segregation of DNA inLife (Basel, Switzerland) · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Biology · 2021
    Article
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  11. Review
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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

5 authors at 1 institution in 1 country.

Emily HelgesenDepartment of Cell Biology, Institute for Cancer Research, Oslo University Hospital, Radiumhospitalet, 0310 Oslo, Norway.
Solveig Fossum-RaunehaugDepartment of Cell Biology, Institute for Cancer Research, Oslo University Hospital, Radiumhospitalet, 0310 Oslo, Norway School of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, 0316 Oslo, Norway.
Frank SætreDepartment of Cell Biology, Institute for Cancer Research, Oslo University Hospital, Radiumhospitalet, 0310 Oslo, Norway.
Kay Oliver SchinkDepartment of Biochemistry, Institute for Cancer Research, Oslo University Hospital, Radiumhospitalet, 0310 Oslo, Norway.
Kirsten SkarstadDepartment of Cell Biology, Institute for Cancer Research, Oslo University Hospital, Radiumhospitalet, 0310 Oslo, Norway School of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, 0316 Oslo, Norway kirsten.skarstad@labmed.uio.no.
Oslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Escherichia coli SeqA protein binds to newly replicated, hemimethylated DNA behind replication forks and forms structures consisting of several hundred SeqA molecules bound to about 100 kb of DNA. It has been suggested that SeqA structures either direct the new sister DNA molecules away from each other or constitute a spacer that keeps the sisters together. We have developed an image analysis script that automatically measures the distance between neighboring foci in cells. Using this tool as well as direct stochastic optical reconstruction microscopy (dSTORM) we find that in cells with fluorescently tagged SeqA and replisome the sister SeqA structures were situated close together (less than about 30 nm apart) and relatively far from the replisome (on average 200-300 nm). The results support the idea that newly replicated sister molecules are kept together behind the fork and suggest the existence of a stretch of DNA between the replisome and SeqA which enjoys added stabilization. This could be important in facilitating DNA transactions such as recombination, mismatch repair and topoisomerase activity. In slowly growing cells without ongoing replication forks the SeqA protein was found to reside at the fully methylated origins prior to initiation of replication.

Indexed as

Bacterial Outer Membrane ProteinsCell CycleCell DivisionChromosomes, BacterialDNA, BacterialDNA-Binding ProteinsDNA ReplicationEscherichia coliEscherichia coli ProteinsFlow CytometryLuminescent ProteinsMicroscopy, FluorescenceModels, GeneticRepliconBacterial Outer Membrane ProteinsDNA, BacterialDNA-Binding ProteinsEscherichia coli ProteinsLuminescent ProteinsSeqA protein, E coliSSB protein, E coli

Identifiers

PMID25722374
PMCPMC4357733
OpenAlexW2129278179

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.