Evidence map›Paper›PMID 18180284›Full record

ArticleMolecular and cellular biology2008

Minichromosome maintenance proteins interact with checkpoint and recombination proteins to promote s-phase genome stability.

Julie M Bailis, Douglas D Luche, Tony Hunter, Susan L Forsburg

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 81 citations in OpenAlex.

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  18. Meiotic Recombination: The Essence of Heredity.Cold Spring Harbor perspectives in biology · 2015
    Review
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

Julie M BailisMolecular and Computational Biology Section, University of Southern California, 1050 Childs Way RRI 201B, Los Angeles, CA 90089-2910, USA.
Douglas D Luche
Tony Hunter
Susan L Forsburg
University of Southern California · USSalk Institute for Biological Studies · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
SOMATIC CELL CYCLE REGULATION BY PHOSPHORYLATIONR01CA080100 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI HUNTER, TONY R. · 1999 to 2018
$13.1M
Salk Institute Cancer Training GrantT32CA009370 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Diana Clare Hargreaves, Jan Karlseder · 1986 to 2026
$8.6M
Genetic Analysis of MSM Protein Function in S. PombeR01GM059321 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FORSBURG, SUSAN L · 1999 to 2012
$4.7M
NCI NIH HHS CA009370NCI NIH HHS CA14195NCI NIH HHS CA80100NCI NIH HHS P30 CA014195NCI NIH HHS R01 CA080100NCI NIH HHS T32 CA009370NIGMS NIH HHS GM059321NIGMS NIH HHS R01 GM059321
6 · The paper itself

Abstract

The minichromosome maintenance (MCM) complex plays essential, conserved roles throughout DNA synthesis: first, as a component of the prereplication complex at origins and, then, as a helicase associated with replication forks. Here we use fission yeast (Schizosaccharomyces pombe) as a model to demonstrate a role for the MCM complex in protecting replication fork structure and promoting recovery from replication arrest. Loss of MCM function generates lethal double-strand breaks at sites of DNA synthesis during replication elongation, suggesting replication fork collapse. MCM function also maintains the stability of forks stalled by hydroxyurea that activate the replication checkpoint. In cells where the checkpoint is activated, Mcm4 binds the Cds1 kinase and undergoes Cds1-dependent phosphorylation. MCM proteins also interact with proteins involved in homologous recombination, which promotes recovery from arrest by ensuring normal mitosis. We suggest that the MCM complex links replication fork stabilization with checkpoint arrest and recovery through direct interactions with checkpoint and recombination proteins and that this role in S-phase genome stability is conserved from yeast to human cells.

Indexed as

Genomic InstabilityS PhaseAmino Acid SubstitutionBleomycinCell Cycle ProteinsCell SurvivalCheckpoint Kinase 2DNA-Binding ProteinsDNA DamageGamma RaysHeLa CellsHumansHydroxyureaMethyl MethanesulfonateMinichromosome Maintenance Complex Component 4MutagensBleomycinCds1 protein, S pombeCell Cycle ProteinsCheckpoint Kinase 2CHEK2 protein, humanDNA-Binding ProteinsHydroxyureamcm4 protein, S pombeMethyl MethanesulfonateMinichromosome Maintenance Complex Component 4MutagensNucleic Acid Synthesis InhibitorsProlineProtein KinasesProtein Serine-Threonine Kinasesrad3 protein, S pombeRad51 RecombinaseRHP51 protein, S pombeRNA, Small InterferingSchizosaccharomyces pombe Proteins

Identifiers

PMID18180284
PMCPMC2258774
OpenAlexW2100064182

What OpenQuestion holds

Textmetadata
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.