Evidence map›Paper›PMID 33443082›Full record

ArticleJournal of cell science2021

A glucose-starvation response governs endocytic trafficking and eisosomal retention of surface cargoes in budding yeast.

Kamilla M E Laidlaw, Daniel D Bisinski, Sviatlana Shashkova, Katherine M Paine, Malaury A Veillon, Mark C Leake, Chris MacDonald

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 40 citations in OpenAlex.

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  8. Increased mesoscale diffusivity in response to acute glucose starvation.bioRxiv : the preprint server for biology · 2023
    Article
  9. Article
  10. The Lipid Profile of theJournal of fungi (Basel, Switzerland) · 2022
    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

7 authors at 1 institution in 1 country.

Kamilla M E LaidlawYork Biomedical Research Institute and Department of Biology, University of York, York, UK.ORCID 0000-0001-9209-4806
Daniel D BisinskiYork Biomedical Research Institute and Department of Biology, University of York, York, UK.ORCID 0000-0001-6762-5070
Sviatlana ShashkovaYork Biomedical Research Institute and Department of Biology, University of York, York, UK.ORCID 0000-0002-4641-3295
Katherine M PaineYork Biomedical Research Institute and Department of Biology, University of York, York, UK.ORCID 0000-0003-3017-4995
Malaury A VeillonYork Biomedical Research Institute and Department of Biology, University of York, York, UK.ORCID 0000-0002-1908-9725
Mark C LeakeYork Biomedical Research Institute and Department of Biology, University of York, York, UK.ORCID 0000-0002-1715-1249
Chris MacDonaldYork Biomedical Research Institute and Department of Biology, University of York, York, UK chris.macdonald@york.ac.uk.ORCID 0000-0002-7450-600X
University of York · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R001235/1MCCC_/Marie Curie/United Kingdom ITN REF. 764591Wellcome TrustWellcome Trust 204636/Z/16/Z
6 · The paper itself

Abstract

Eukaryotic cells adapt their metabolism to the extracellular environment. Downregulation of surface cargo proteins in response to nutrient stress reduces the burden of anabolic processes whilst elevating catabolic production in the lysosome. We show that glucose starvation in yeast triggers a transcriptional response that increases internalisation from the plasma membrane. Nuclear export of the Mig1 transcriptional repressor in response to glucose starvation increases levels of the Yap1801 and Yap1802 clathrin adaptors, which is sufficient to increase cargo internalisation. Beyond this, we show that glucose starvation results in Mig1-independent transcriptional upregulation of various eisosomal factors. These factors serve to sequester a portion of nutrient transporters at existing eisosomes, through the presence of Ygr130c and biochemical and biophysical changes in Pil1, allowing cells to persist throughout the starvation period and maximise nutrient uptake upon return to replete conditions. This provides a physiological benefit for cells to rapidly recover from glucose starvation. Collectively, this remodelling of the surface protein landscape during glucose starvation calibrates metabolism to available nutrients.This article has an associated First Person interview with the first author of the paper.

Indexed as

Saccharomyces cerevisiae ProteinsSaccharomycetalesCell MembraneGlucosePhosphoproteinsRepressor ProteinsSaccharomyces cerevisiaeGlucoseMIG1 protein, S cerevisiaePhosphoproteinsPIL1 protein, S cerevisiaeRepressor ProteinsSaccharomyces cerevisiae ProteinsEisosomesEndosomal traffickingGlucose starvationMembrane trafficking

Identifiers

PMID33443082
PMCPMC7860119
OpenAlexW3114186555

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.