Evidence map›Paper›PMID 15229282›Full record

ArticleMolecular biology of the cell2004

A role for Saccharomyces cerevisiae Chk1p in the response to replication blocks.

Kaila L Schollaert, Julie M Poisson, Jennifer S Searle, Jennifer A Schwanekamp, Craig R Tomlinson, Yolanda Sanchez

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Of mice, genes and aging.Haematologica · 2020
    Article
  3. Article
  4. Article
  5. ATRMec1 phosphorylation-independent activation of Chk1 in vivo.The Journal of biological chemistry · 2009
    Article
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  7. Article
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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

6 authors at 2 institutions in 1 country.

Kaila L SchollaertDepartment of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Cincinnati, OH 45267-0524, USA.
Julie M Poisson
Jennifer S Searle
Jennifer A Schwanekamp
Craig R Tomlinson
Yolanda Sanchez
University of Cincinnati Medical Center · USUniversity of Cincinnati · US

Funding

REPRODUCTIVE AND DEVELOPMENTAL TOXICOLOGY RESEARCHP30ES006096 · NIEHS · UNIVERSITY OF CINCINNATI · PI YADAV, JAGJIT S · 1992 to 2022
$35.4M
Plk3 variants in transgenic mice and MEFsU01ES011038 · NIEHS · UNIVERSITY OF CINCINNATI · PI STAMBROOK, PETER J. · 2001 to 2006
$6.7M
NIEHS NIH HHS ES11038NIEHS NIH HHS P30 ES006096NIEHS NIH HHS P30 ES06096NIEHS NIH HHS U01 ES011038
6 · The paper itself

Abstract

Replication blocks and DNA damage incurred during S phase activate the S-phase and intra-S-phase checkpoint responses, respectively, regulated by the Atrp and Chk1p checkpoint kinases in metazoans. In Saccharomyces cerevisiae, these checkpoints are regulated by the Atrp homologue Mec1p and the kinase Rad53p. A conserved role of these checkpoints is to block mitotic progression until DNA replication and repair are completed. In S. cerevisiae, these checkpoints include a transcriptional response regulated by the kinase Dun1p; however, dun1Delta cells are proficient for the S-phase-checkpoint-induced anaphase block. Yeast Chk1p kinase regulates the metaphase-to-anaphase transition in the DNA-damage checkpoint pathway via securin (Pds1p) phosphorylation. However, like Dun1p, yeast Chk1p is not required for the S-phase-checkpoint-induced anaphase block. Here we report that Chk1p has a role in the intra-S-phase checkpoint activated when yeast cells replicate their DNA in the presence of low concentrations of hydroxyurea (HU). Chk1p was modified and Pds1p was transiently phosphorylated in this response. Cells lacking Dun1p were dependent on Chk1p for survival in HU, and chk1Delta dun1Delta cells were defective in the recovery from replication interference caused by transient HU exposure. These studies establish a relationship between the S-phase and DNA-damage checkpoint pathways in S. cerevisiae and suggest that at least in some genetic backgrounds, the Chk1p/securin pathway is required for the recovery from stalled or collapsed replication forks.

Indexed as

Base SequenceCell Cycle ProteinsCheckpoint Kinase 1DNA DamageDNA, FungalDNA ReplicationGenes, FungalHydroxyureaMutationNuclear ProteinsProtein KinasesProtein Serine-Threonine KinasesRibonucleotide ReductasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSecurinCell Cycle ProteinsCheckpoint Kinase 1DNA, FungalDUN1 protein, S cerevisiaeHydroxyureaNuclear ProteinsPDS1 protein, S cerevisiaeProtein KinasesProtein Serine-Threonine KinasesRibonucleotide ReductasesSaccharomyces cerevisiae ProteinsSecurin

Identifiers

PMID15229282
PMCPMC515340
OpenAlexW2143805336

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.