Evidence map›Paper›PMID 16387872›Full record

ArticleGenetics2006

Regulation of the oxidative stress response through Slt2p-dependent destruction of cyclin C in Saccharomyces cerevisiae.

Elizabeth Krasley, Katrina F Cooper, Michael J Mallory, Roland Dunbrack, Randy Strich

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

36 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Manganese Stress Tolerance Depends on Yap1 and Stress-Activated MAP Kinases.International journal of molecular sciences · 2022
    Article
  3. Substrates of the MAPK Slt2: Shaping Yeast Cell Integrity.Journal of fungi (Basel, Switzerland) · 2022
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. TheG3 (Bethesda, Md.) · 2017
    Article
  15. Article
  16. Article
  17. Review
  18. 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

5 authors at 2 institutions in 1 country.

Elizabeth KrasleyInstitute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.
Katrina F Cooper
Michael J Mallory
Roland Dunbrack
Randy Strich
Fox Chase Cancer Center · USDrexel University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Role of the Oxidative Stress Pathway in Drug ResistanceR01CA099003 · NCI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI STRICH, RANDY S · 2003 to 2007
$1.4M
REGULATION OF C-TYPE CYCLINS IN YEASTR01GM057842 · NIGMS · INSTITUTE FOR CANCER RESEARCH · PI STRICH, RANDY S · 1999 to 2002
$1.1M
Role of the Oxidative Stress Pathway in Drug ResistanceR56CA099003 · NCI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI STRICH, RANDY S · 2009 to 2009
$351k
NCI NIH HHS CA 06927NCI NIH HHS CA99003NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA099003NCI NIH HHS R56 CA099003NIGMS NIH HHS GM57842NIGMS NIH HHS R01 GM057842
6 · The paper itself

Abstract

The Saccharomyces cerevisiae C-type cyclin and its cyclin-dependent kinase (Cdk8p) repress the transcription of several stress response genes. To relieve this repression, cyclin C is destroyed in cells exposed to reactive oxygen species (ROS). This report describes the requirement of cyclin C destruction for the cellular response to ROS. Compared to wild type, deleting cyclin C makes cells more resistant to ROS while its stabilization reduces viability. The Slt2p MAP kinase cascade mediates cyclin C destruction in response to ROS treatment but not heat shock. This destruction pathway is important as deleting cyclin C suppresses the hypersensitivity of slt2 mutants to oxidative damage. The ROS hypersensitivity of an slt2 mutant correlates with elevated programmed cell death as determined by TUNEL assays. Consistent with the viability studies, the elevated TUNEL signal is reversed in cyclin C mutants. Finally, two results suggest that cyclin C regulates programmed cell death independently of its function as a transcriptional repressor. First, deleting its corepressor CDK8 does not suppress the slt2 hypersensitivity phenotype. Second, the human cyclin C, which does not repress transcription in yeast, does regulate ROS sensitivity. These findings demonstrate a new role for the Slt2p MAP kinase cascade in protecting the cell from programmed cell death through cyclin C destruction.

Indexed as

Suppression, GeneticAmino Acid SubstitutionApoptosisCyclin CCyclin-Dependent Kinase 8Cyclin-Dependent KinasesCyclinsHumansHydrogen PeroxideMAP Kinase Signaling SystemMitogen-Activated Protein KinasesOxidative StressProtein Kinase CReactive Oxygen SpeciesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCCNC protein, humanCyclin CCyclin-Dependent Kinase 8Cyclin-Dependent KinasesCyclinsHydrogen PeroxideMitogen-Activated Protein KinasesPKC1 protein, S cerevisiaeProtein Kinase CReactive Oxygen SpeciesSaccharomyces cerevisiae ProteinsSLT2 protein, S cerevisiaeSSN3 protein, S cerevisiae

Identifiers

PMID16387872
PMCPMC1456298
OpenAlexW2169767854

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.