Evidence map›Paper›PMID 25411338›Full record

ArticleMolecular biology of the cell2015

Mechanisms of expression and translocation of major fission yeast glucose transporters regulated by CaMKK/phosphatases, nuclear shuttling, and TOR.

Shigeaki Saitoh, Ayaka Mori, Lisa Uehara, Fumie Masuda, Saeko Soejima, Mitsuhiro Yanagida

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.4field-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

37 citing papers in PubMed, 67 citations in OpenAlex.

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  13. Mitotic spindle formation in the absence of Polo kinase.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

6 authors at 2 institutions in 1 country.

Shigeaki SaitohInstitute of Life Science, Kurume University, Hyakunen-Kohen 1-1, Kurume, Fukuoka 839-0864, Japan saitou_shigeaki@kurume-u.ac.jp myanagid@gmail.com.
Ayaka MoriOkinawa Institute Science and Technology Graduate University, Tancha 1919-1, Onna, Okinawa 904-0495, Japan.
Lisa UeharaOkinawa Institute Science and Technology Graduate University, Tancha 1919-1, Onna, Okinawa 904-0495, Japan.
Fumie MasudaInstitute of Life Science, Kurume University, Hyakunen-Kohen 1-1, Kurume, Fukuoka 839-0864, Japan.
Saeko SoejimaInstitute of Life Science, Kurume University, Hyakunen-Kohen 1-1, Kurume, Fukuoka 839-0864, Japan.
Mitsuhiro YanagidaOkinawa Institute Science and Technology Graduate University, Tancha 1919-1, Onna, Okinawa 904-0495, Japan saitou_shigeaki@kurume-u.ac.jp myanagid@gmail.com.
Kurume University · JPOkinawa Institute of Science and Technology Graduate University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hexose transporters are required for cellular glucose uptake; thus they play a pivotal role in glucose homeostasis in multicellular organisms. Using fission yeast, we explored hexose transporter regulation in response to extracellular glucose concentrations. The high-affinity transporter Ght5 is regulated with regard to transcription and localization, much like the human GLUT transporters, which are implicated in diabetes. When restricted to a glucose concentration equivalent to that of human blood, the fission yeast transcriptional regulator Scr1, which represses Ght5 transcription in the presence of high glucose, is displaced from the nucleus. Its displacement is dependent on Ca(2+)/calmodulin-dependent kinase kinase, Ssp1, and Sds23 inhibition of PP2A/PP6-like protein phosphatases. Newly synthesized Ght5 locates preferentially at the cell tips with the aid of the target of rapamycin (TOR) complex 2 signaling. These results clarify the evolutionarily conserved molecular mechanisms underlying glucose homeostasis, which are essential for preventing hyperglycemia in humans.

Indexed as

Active Transport, Cell NucleusCalcium-Calmodulin-Dependent Protein Kinase KinaseCell Cycle ProteinsCell NucleusGene Expression Regulation, FungalGlucoseGlucose Transport Proteins, FacilitativeGreen Fluorescent ProteinsHSP70 Heat-Shock ProteinsHumansImmunoblottingMechanistic Target of Rapamycin Complex 2Microscopy, FluorescenceMonosaccharide Transport ProteinsMultiprotein ComplexesMutationCalcium-Calmodulin-Dependent Protein Kinase KinaseCell Cycle ProteinsGht5 protein, S pombeGlucoseGlucose Transport Proteins, FacilitativeGreen Fluorescent ProteinsHSP70 Heat-Shock ProteinsMechanistic Target of Rapamycin Complex 2Monosaccharide Transport ProteinsMultiprotein ComplexesPhosphoprotein PhosphatasesProtein IsoformsPSS1 protein, S pombeSchizosaccharomyces pombe ProteinsSds23 protein, S pombeTOR Serine-Threonine Kinases

Identifiers

PMID25411338
PMCPMC4294683
OpenAlexW2072500799

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.