Evidence map›Paper›PMID 24821015›Full record

ArticleBiochimica et biophysica acta2014

Glucose starvation-induced turnover of the yeast glucose transporter Hxt1.

Adhiraj Roy, Yong-Bae Kim, Kyu Hong Cho, Jeong-Ho Kim

Abstract read
In one paragraph

Article in Biochimica et biophysica acta, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
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  10. Review
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  13. Effects ofMolecular medicine reports · 2021
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Engineering of Pentose Transport inFrontiers in bioengineering and biotechnology · 2019
    Review
  19. Article
  20. 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.

Adhiraj RoyDepartment of Biochemistry and Molecular Medicine, The George Washington University Medical Center, 2300 Eye Street, Washington, DC 20037, USA.
Yong-Bae KimDepartment of Biochemistry and Molecular Medicine, The George Washington University Medical Center, 2300 Eye Street, Washington, DC 20037, USA.
Kyu Hong ChoDepartment of Microbiology, Southern Illinois University Carbondale, 1125 Lincoln Drive, Carbondale, IL 62901, USA.
Jeong-Ho KimDepartment of Biochemistry and Molecular Medicine, The George Washington University Medical Center, 2300 Eye Street, Washington, DC 20037, USA. Electronic address: jh_kim@gwu.edu.

Funding

Crosstalk between the glucose signaling pathways in yeastR01GM087470 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI KIM, JEONG-HO · 2009 to 2013
$1.1M
Receptor-mediated glucose sensing in yeastR15GM134447 · NIGMS · LIBERTY UNIVERSITY, INC. · PI KIM, JEONG-HO · 2019 to 2025
$948k
NIGMS NIH HHS GM087470NIGMS NIH HHS R01 GM087470NIGMS NIH HHS R15 GM134447
6 · The paper itself

Abstract

backgroundThe budding yeast Saccharomyces cerevisiae possesses multiple glucose transporters with different affinities for glucose that enable it to respond to a wide range of glucose concentrations. The steady-state levels of glucose transporters are regulated in response to changes in the availability of glucose. This study investigates the glucose regulation of the low affinity, high capacity glucose transporter Hxt1. METHODS AND

resultsWestern blotting and confocal microscopy were performed to evaluate glucose regulation of the stability of Hxt1. Our results show that glucose starvation induces endocytosis and degradation of Hxt1 and that this event requires End3, a protein required for endocytosis, and the Doa4 deubiquitination enzyme. Mutational analysis of the lysine residues in the Hxt1 N-terminal domain demonstrates that the two lysine residues, K12 and K39, serve as the putative ubiquitin-acceptor sites by the Rsp5 ubiquitin ligase. We also demonstrate that inactivation of PKA (cAMP-dependent protein kinase A) is needed for Hxt1 turnover, implicating the role of the Ras/cAMP-PKA glucose signaling pathway in the stability of Hxt1. CONCLUSION AND GENERAL SIGNIFICANCE: Hxt1, most useful when glucose is abundant, is internalized and degraded when glucose becomes depleted. Of note, the stability of Hxt1 is regulated by PKA, known as a positive regulator for glucose induction of HXT1 gene expression, demonstrating a dual role of PKA in regulation of Hxt1.

Indexed as

Cyclic AMP-Dependent Protein KinasesCytoskeletal ProteinsEndocytosisEndopeptidasesEndosomal Sorting Complexes Required for TransportGene Expression Regulation, FungalGlucoseGlucose Transport Proteins, FacilitativeProtein Structure, TertiarySaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionUbiquitin ThiolesteraseCyclic AMP-Dependent Protein KinasesCytoskeletal ProteinsDOA4 protein, S cerevisiaeEND3 protein, S cerevisiaeEndopeptidasesEndosomal Sorting Complexes Required for TransportGlucoseGlucose Transport Proteins, FacilitativeHXT1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsUbiquitin ThiolesteraseEndocytosisGlucose transporterHxt1Yeast

Identifiers

PMID24821015
PMCPMC4127130

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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.