Evidence map›Paper›PMID 24811316›Full record

ReviewSeminars in cell & developmental biology2014

Mechanism and physiological significance of programmed replication termination.

Deepak Bastia, Shamsu Zaman

Abstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Mechanisms of DNA replication termination.Nature reviews. Molecular cell biology · 2017
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Phosphorylation of CMG helicase and Tof1 is required for programmed fork arrest.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  14. Article
  15. Article
  16. Review
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

2 authors.

Deepak BastiaDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, United States. Electronic address: bastia@musc.edu.
Shamsu ZamanDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, United States.

Funding

Control of Programmed Replication fork Arrest by Chromosome KissingR01GM098013 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BASTIA, DEEPAK · 2011 to 2014
$1.6M
NIGMS NIH HHS 5R01GM098013-04NIGMS NIH HHS R01 GM098013
6 · The paper itself

Abstract

Replication forks in both prokaryotic and eukaryotic systems pause at random sites due to depletion of dNTP pools, DNA damage, tight binding nonhistone proteins or unusual DNA sequences and/or structures, in a mostly non-polar fashion. However, there is also physiologically programmed replication termination at sequence-specific authentic replication termini. Here, the structure and functions of programmed replication termini, their mechanism of action and their diverse physiological functions in prokaryotes and eukaryotes have been reviewed.

Indexed as

DNA ReplicationAmino Acid SubstitutionAnimalsBacteriaBacterial ProteinsBase SequenceDNA, BacterialGene SilencingHumansModels, MolecularSaccharomyces cerevisiae ProteinsBacterial ProteinsDNA, BacterialSaccharomyces cerevisiae ProteinsCrystal structureGene silencingRecombinationReplication terminationReplicative agingTerminator protein

Identifiers

PMID24811316
PMCPMC4077545

What OpenQuestion holds

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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.