Evidence map›Paper›PMID 29298091›Full record

ReviewAnnual review of biochemistry2018

Lesion Bypass and the Reactivation of Stalled Replication Forks.

Kenneth J Marians

Abstract readReview
In one paragraph

Review in Annual review of biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing 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

121 citing papers in PubMed.

  1. Article
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  3. Review
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  9. Review
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  15. Article
  16. The Role of the RecFOR Complex in Genome Stability.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Article
  19. Review
  20. Article

61 more citing papers are in PubMed but not listed here.

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

1 author.

Kenneth J MariansMolecular Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA; email: kmarians@sloankettering.edu.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Mechanisms of DNA Replication, Chromosome Compaction, and Chromosome UnlinkingR35GM126907 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI KENNETH J MARIANS · 2018 to 2026
$8.8M
Topoisomerases, Condensins, and Chromosome SegregationR01GM034558 · NIGMS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI MARIANS, KENNETH J · 1985 to 2017
$6.6M
MECHANISMS OF DNA REPLICATIONR37GM034557 · NIGMS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI MARIANS, KENNETH J · 2001 to 2010
$5.8M
MECHANISMS OF LAGGING STRAND SYNTHESISR01GM034557 · NIGMS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI MARIANS, KENNETH J · 1985 to 2018
$5.7M
NCI NIH HHS P30 CA008748NIGMS NIH HHS R01 GM034557NIGMS NIH HHS R01 GM034558NIGMS NIH HHS R35 GM126907NIGMS NIH HHS R37 GM034557
6 · The paper itself

Abstract

Accurate transmission of the genetic information requires complete duplication of the chromosomal DNA each cell division cycle. However, the idea that replication forks would form at origins of DNA replication and proceed without impairment to copy the chromosomes has proven naive. It is now clear that replication forks stall frequently as a result of encounters between the replication machinery and template damage, slow-moving or paused transcription complexes, unrelieved positive superhelical tension, covalent protein-DNA complexes, and as a result of cellular stress responses. These stalled forks are a major source of genome instability. The cell has developed many strategies for ensuring that these obstructions to DNA replication do not result in loss of genetic information, including DNA damage tolerance mechanisms such as lesion skipping, whereby the replisome jumps the lesion and continues downstream; template switching both behind template damage and at the stalled fork; and the error-prone pathway of translesion synthesis.

Indexed as

DNA DamageDNA RepairDNA ReplicationDNA, BacterialDNA-Directed DNA PolymeraseEscherichia coliGenomic InstabilityHumansModels, BiologicalDNA, BacterialDNA-Directed DNA PolymeraseDNA lesionlesion skippingreplication fork reversalreplication fork stallingreplication restarttemplate switchingtranslesion synthesis

Identifiers

PMID29298091
PMCPMC6419508

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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.