Evidence map›Paper›PMID 38002301›Full record

ArticleBiomolecules2023

Elevated Levels of Mislocalised, Constitutive Ras Signalling Can Drive Quiescence by Uncoupling Cell-Cycle Regulation from Metabolic Homeostasis.

Elliot Piper-Brown, Fiona Dresel, Eman Badr, Campbell W Gourlay

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Microbial cell (Graz, Austria) · 2026
    Article
  2. Article
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

4 authors at 1 institution in 1 country.

Elliot Piper-BrownKent Fungal Group, School of Biosciences, University of Kent, Canterbury CT2 7NZ, UK.
Fiona DreselKent Fungal Group, School of Biosciences, University of Kent, Canterbury CT2 7NZ, UK.ORCID 0009-0005-4771-7652
Eman BadrKent Fungal Group, School of Biosciences, University of Kent, Canterbury CT2 7NZ, UK.ORCID 0000-0002-5221-1200
Campbell W GourlayKent Fungal Group, School of Biosciences, University of Kent, Canterbury CT2 7NZ, UK.ORCID 0000-0002-2373-6788
University of Kent · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M015785/1
6 · The paper itself

Abstract

The small GTPase Ras plays an important role in connecting external and internal signalling cues to cell fate in eukaryotic cells. As such, the loss of RAS regulation, localisation, or expression level can drive changes in cell behaviour and fate. Post-translational modifications and expression levels are crucial to ensure Ras localisation, regulation, function, and cell fate, exemplified by RAS mutations and gene duplications that are common in many cancers. Here, we reveal that excessive production of yeast Ras2, in which the phosphorylation-regulated serine at position 225 is replaced with alanine or glutamate, leads to its mislocalisation and constitutive activation. Rather than inducing cell death, as has been widely reported to be a consequence of constitutive Ras2 signalling in yeast, the overexpression of

Indexed as

Saccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCyclic AMPFungal ProteinsHomeostasisras ProteinsCyclic AMPFungal Proteinsras ProteinsSaccharomyces cerevisiae Proteinscell fatemetabolismRasyeast signallingyquiescence

Identifiers

PMID38002301
PMCPMC10669370
OpenAlexW4388410947

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.