Evidence map›Paper›PMID 23071099›Full record

ArticleMolecular & cellular proteomics : MCP2013

RACK1/Asc1p, a ribosomal node in cellular signaling.

Nicole Rachfall, Kerstin Schmitt, Susanne Bandau, Nadine Smolinski, Armin Ehrenreich, Oliver Valerius, Gerhard H Braus

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

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  11. Capturing the Asc1p/Molecular & cellular proteomics : MCP · 2017
    Article
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  16. Review
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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

7 authors at 1 institution in 1 country.

Nicole RachfallInstitute of Microbiology and Genetics, Georg-August Universität, D-37077 Göttingen, Germany.
Kerstin Schmitt
Susanne Bandau
Nadine Smolinski
Armin Ehrenreich
Oliver Valerius
Gerhard H Braus
University of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RACK1/Asc1p and its essential orthologues in higher eukaryotes, such as RACK1 in metazoa, are involved in several distinct cellular signaling processes. The implications of a total deletion have never been assessed in a comprehensive manner. This study reveals the major cellular processes affected in a Saccharomyces cerevisiae Δasc1 deletion background via de novo proteome and transcriptome analysis, as well as subsequent phenotypical characterizations. The deletion of ASC1 reduces iron uptake and causes nitrosative stress, both known indicators for hypoxia, which manifests in a shift of energy metabolism from respiration to fermentation in the Δasc1 strain. Asc1p further impacts cellular metabolism through its regulative role in the MAP kinase signal transduction pathways of invasive/filamentous growth and cell wall integrity. In the Δasc1 mutant strain, aberrations from the expected cellular response, mediated by these pathways, can be observed and are linked to changes in protein abundances of pathway-targeted transcription factors. Evidence of the translational regulation of such transcription factors suggests that ribosomal Asc1p is involved in signal transduction pathways and controls the biosynthesis of the respective final transcriptional regulators.

Indexed as

Energy MetabolismAdaptor Proteins, Signal TransducingBiological TransportFermentationGene DeletionGene Expression ProfilingIronMAP Kinase Signaling SystemMitogen-Activated Protein KinasesOxygen ConsumptionPeptidesReceptors for Activated C KinaseRibosomesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscriptomeAdaptor Proteins, Signal TransducingIronMitogen-Activated Protein Kinasespeptide IPeptidesReceptors for Activated C KinaseSaccharomyces cerevisiae Proteins

Identifiers

PMID23071099
PMCPMC3536911
OpenAlexW2143196802

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.