Evidence map›Paper›PMID 17041188›Full record

ArticleEukaryotic cell2006

Pheromone-induced degradation of Ste12 contributes to signal attenuation and the specificity of developmental fate.

R Keith Esch, Yuqi Wang, Beverly Errede

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Kar4 acts as a Ste12 regulator inbioRxiv : the preprint server for biology · 2025
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  5. Identifying genetic modulators of the connectivity between transcription factors and their transcriptional targets.Proceedings of the National Academy of Sciences of the United States of America · 2016
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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

3 authors at 2 institutions in 1 country.

R Keith EschDepartment of Biochemistry and Biophysics, CB 7260 512 ME Jones, University of North Carolina, Chapel Hill, NC 27599-7260, USA.
Yuqi Wang
Beverly Errede
University of North Carolina at Chapel Hill · USSaint Louis University · US

Funding

Cell-fate determinants of yeast pseudohyphal growthR01GM067809 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI ERREDE, BEVERLY · 2003 to 2005
$945k
KINASES AND CONTROL OF CELL-TYPE SPECIALIZATIONR01GM039852 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI ERREDE, BEVERLY · 1988 to 2002
$900k
NIGMS NIH HHS GM067809NIGMS NIH HHS GM39852NIGMS NIH HHS R01 GM067809
6 · The paper itself

Abstract

The Ste12 transcription factor of Saccharomyces cerevisiae regulates transcription programs controlling two different developmental fates. One is differentiation into a mating-competent form that occurs in response to mating pheromone. The other is the transition to a filamentous-growth form that occurs in response to nutrient deprivation. These two distinct roles for Ste12 make it a focus for studies into regulatory mechanisms that impart biological specificity. The transient signal characteristic of mating differentiation led us to test the hypothesis that regulation of Ste12 turnover might contribute to attenuation of the mating-specific transcription program and restrict activation of the filamentation program. We show that prolonged pheromone induction leads to ubiquitin-mediated destabilization and decreased amounts of Ste12. This depletion in pheromone-stimulated cultures is dependent on the mating-pathway-dedicated mitogen-activated protein kinase Fus3 and its target Cdc28 inhibitor, Far1. Attenuation of pheromone-induced mating-specific gene transcription (FUS1) temporally correlates with Ste12 depletion. This attenuation is abrogated in the deletion backgrounds (fus3Delta or far1Delta) where Ste12 is found to persist. Additionally, pheromone induces haploid invasion and filamentous-like growth instead of mating differentiation when Ste12 levels remain high. These observations indicate that loss of Ste12 reinforces the adaptive response to pheromone and contributes to the curtailing of a filamentation response.

Indexed as

Base SequenceCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor ProteinsDNA, FungalGenes, FungalHaploidyMating FactorMitogen-Activated Protein KinasesPeptidesRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionTranscription FactorsTranscription, GeneticUbiquitinCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor ProteinsDNA, FungalFAR1 protein, S cerevisiaeFUS3 protein, S cerevisiaeMating FactorMitogen-Activated Protein KinasesPeptidesRepressor ProteinsSaccharomyces cerevisiae ProteinsSTE12 protein, S cerevisiaeTranscription FactorsUbiquitin

Identifiers

PMID17041188
PMCPMC1694826
OpenAlexW2105131686

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.