Evidence map›Paper›PMID 11598186›Full record

ArticleMolecular biology of the cell2001

Genomic expression responses to DNA-damaging agents and the regulatory role of the yeast ATR homolog Mec1p.

A P Gasch, M Huang, S Metzner, D Botstein, S J Elledge, P O Brown

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular biology of the cell, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 257 papers.

0numbers the graph read from it
0cells of the map it votes in
257citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

257 citing papers in PubMed, 545 citations in OpenAlex.

  1. Review
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  12. International journal of molecular sciences · 2022
    Review
  13. Article
  14. Transcriptional Profiling of theInternational journal of molecular sciences · 2022
    Article
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197 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

6 authors at 2 institutions in 1 country.

A P GaschDepartments of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA.
M Huang
S Metzner
D Botstein
S J Elledge
P O Brown
Stanford University · USUniversity of Colorado Hospital · US

Funding

Genetics of Functional Interactions in YeastR01GM046406 · NIGMS · STANFORD UNIVERSITY · PI BOTSTEIN, DAVID · 2001 to 2015
$9.5M
Genetics of Cell Cycle &DNA Damage Regulation in YeastR37GM044664 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ELLEDGE, STEPHEN J · 2003 to 2012
$3.5M
GENETICS OF CELL CYCLE &DNA DAMAGE REGULATION IN YEASTR01GM044664 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ELLEDGE, STEPHEN J · 1990 to 2016
$2.0M
FUNCTIONAL MAP OF THE YEAST GENOMER01HG000983 · NHGRI · STANFORD UNIVERSITY · PI BROWN, PATRICK O. · 1996 to 2001
$1.0M
GENETICS OF FUNCTIONAL INTERACTIONS IN YEASTR37GM046406 · NIGMS · STANFORD UNIVERSITY · PI BOTSTEIN, DAVID · 1991 to 2000
$683k
EFFICIENT GENE MAPPING BY WHOLE GENOME MISMATCH SCANNINGR21HG000450 · NHGRI · STANFORD UNIVERSITY · PI BROWN, PATRICK O. · 1991 to 1993
–
APPLYING GENOMIC MISMATCH SCANNING TO THE GENOMER01HG000450 · NHGRI · STANFORD UNIVERSITY · PI BROWN, PATRICK O. · 1994 to 1999
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NHGRI NIH HHS HG-00450NHGRI NIH HHS HG-00983NIGMS NIH HHS GM-44664NIGMS NIH HHS GM-46406NIGMS NIH HHS R01 GM044664NIGMS NIH HHS R01 GM046406NIGMS NIH HHS R37 GM044664NIGMS NIH HHS R37 GM046406
6 · The paper itself

Abstract

Eukaryotic cells respond to DNA damage by arresting the cell cycle and modulating gene expression to ensure efficient DNA repair. The human ATR kinase and its homolog in yeast, MEC1, play central roles in transducing the damage signal. To characterize the role of the Mec1 pathway in modulating the cellular response to DNA damage, we used DNA microarrays to observe genomic expression in Saccharomyces cerevisiae responding to two different DNA-damaging agents. We compared the genome-wide expression patterns of wild-type cells and mutants defective in Mec1 signaling, including mec1, dun1, and crt1 mutants, under normal growth conditions and in response to the methylating-agent methylmethane sulfonate (MMS) and ionizing radiation. Here, we present a comparative analysis of wild-type and mutant cells responding to these DNA-damaging agents, and identify specific features of the gene expression responses that are dependent on the Mec1 pathway. Among the hundreds of genes whose expression was affected by Mec1p, one set of genes appears to represent an MEC1-dependent expression signature of DNA damage. Other aspects of the genomic responses were independent of Mec1p, and likely independent of DNA damage, suggesting the pleiotropic effects of MMS and ionizing radiation. The complete data set as well as supplemental materials is available at http://www-genome.stanford.edu/mec1.

Indexed as

Radiation, IonizingSaccharomyces cerevisiae ProteinsCell Cycle ProteinsDNA DamageDNA, FungalDNA RepairFungal ProteinsGene Expression Regulation, FungalIntracellular Signaling Peptides and ProteinsMethyl MethanesulfonateMutationOligonucleotide Array Sequence AnalysisProtein KinasesProtein Serine-Threonine KinasesSaccharomyces cerevisiaeSequence HomologyCell Cycle ProteinsDNA, FungalFungal ProteinsIntracellular Signaling Peptides and ProteinsMEC1 protein, S cerevisiaeMethyl MethanesulfonateProtein KinasesProtein Serine-Threonine KinasesSaccharomyces cerevisiae Proteins

Identifiers

PMID11598186
PMCPMC60150
OpenAlexW2162735386

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.