Evidence map›Paper›PMID 10233147›Full record

ArticleMolecular biology of the cell1999

Crosstalk between the Ras2p-controlled mitogen-activated protein kinase and cAMP pathways during invasive growth of Saccharomyces cerevisiae.

H U Mösch, E Kübler, S Krappmann, G R Fink, G H Braus

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

83 citing papers in PubMed, 194 citations in OpenAlex.

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23 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

5 authors at 2 institutions in 2 countries.

H U MöschInstitute for Microbiology and Genetics, Georg-August-University, D-37077 Göttingen, Germany.
E Kübler
S Krappmann
G R Fink
G H Braus
University of Göttingen · DEWhitehead Institute for Biomedical Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The two highly conserved RAS genes of the budding yeast Saccharomyces cerevisiae are redundant for viability. Here we show that haploid invasive growth development depends on RAS2 but not RAS1. Ras1p is not sufficiently expressed to induce invasive growth. Ras2p activates invasive growth using either of two downstream signaling pathways, the filamentation MAPK (Cdc42p/Ste20p/MAPK) cascade or the cAMP-dependent protein kinase (Cyr1p/cAMP/PKA) pathway. This signal branch point can be uncoupled in cells expressing Ras2p mutant proteins that carry amino acid substitutions in the adenylyl cyclase interaction domain and therefore activate invasive growth solely dependent on the MAPK cascade. Both Ras2p-controlled signaling pathways stimulate expression of the filamentation response element-driven reporter gene depending on the transcription factors Ste12p and Tec1p, indicating a crosstalk between the MAPK and the cAMP signaling pathways in haploid cells during invasive growth.

Indexed as

FMN ReductaseSaccharomyces cerevisiae ProteinsAdenylyl CyclasesAmino Acid SequenceBinding SitesCalcium-Calmodulin-Dependent Protein Kinasescdc42 GTP-Binding Protein, Saccharomyces cerevisiaeCell Cycle ProteinsConserved SequenceCyclic AMPCyclic AMP-Dependent Protein KinasesDNA-Binding ProteinsFungal ProteinsGene Expression Regulation, FungalGenes, ReporterGenes, SuppressorAdenylyl CyclasesCalcium-Calmodulin-Dependent Protein Kinasescdc42 GTP-Binding Protein, Saccharomyces cerevisiaeCell Cycle ProteinsCyclic AMPCyclic AMP-Dependent Protein KinasesDNA-Binding Proteinsferric citrate iron reductaseFMN ReductaseFungal ProteinsGTP-Binding ProteinsIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase KinasesNADH, NADPH OxidoreductasesProtein Serine-Threonine KinasesRAS1 protein, S cerevisiaeRAS2 protein, S cerevisiaeras ProteinsSaccharomyces cerevisiae ProteinsSTE12 protein, S cerevisiaeSTE20 protein, S cerevisiaeTEC1 protein, S cerevisiaeTranscription Factors

Identifiers

PMID10233147
PMCPMC25273
OpenAlexW2104720774

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.