Evidence map›Paper›PMID 22290422›Full record

ArticleCell research2012

Glucose-induced posttranslational activation of protein phosphatases PP2A and PP1 in yeast.

Dries Castermans, Ils Somers, Johan Kriel, Wendy Louwet, Stefaan Wera, Matthias Versele, Veerle Janssens, Johan M Thevelein

Open access · hybridAbstract read
In one paragraph

Article in Cell research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 89 citations in OpenAlex.

  1. Glucose repression ofbioRxiv : the preprint server for biology · 2026
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  8. D-Xylose Sensing inInternational journal of molecular sciences · 2021
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  13. Review
  14. Fine-Tuning of Energy Levels RegulatesFrontiers in physiology · 2020
    Article
  15. Article
  16. Review
  17. Article
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  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

8 authors at 3 institutions in 3 countries.

Dries CastermansLaboratory of Molecular Cell Biology, Institute of Botany and Microbiology, KULeuven, Belgium.
Ils Somers
Johan Kriel
Wendy Louwet
Stefaan Wera
Matthias Versele
Veerle Janssens
Johan M Thevelein
KU Leuven · BEJohnson & Johnson (United States) · USVIB-KU Leuven Center for Microbiology · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein phosphatases PP2A and PP1 are major regulators of a variety of cellular processes in yeast and other eukaryotes. Here, we reveal that both enzymes are direct targets of glucose sensing. Addition of glucose to glucose-deprived yeast cells triggered rapid posttranslational activation of both PP2A and PP1. Glucose activation of PP2A is controlled by regulatory subunits Rts1, Cdc55, Rrd1 and Rrd2. It is associated with rapid carboxymethylation of the catalytic subunits, which is necessary but not sufficient for activation. Glucose activation of PP1 was fully dependent on regulatory subunits Reg1 and Shp1. Absence of Gac1, Glc8, Reg2 or Red1 partially reduced activation while Pig1 and Pig2 inhibited activation. Full activation of PP2A and PP1 was also dependent on subunits classically considered to belong to the other phosphatase. PP2A activation was dependent on PP1 subunits Reg1 and Shp1 while PP1 activation was dependent on PP2A subunit Rts1. Rts1 interacted with both Pph21 and Glc7 under different conditions and these interactions were Reg1 dependent. Reg1-Glc7 interaction is responsible for PP1 involvement in the main glucose repression pathway and we show that deletion of Shp1 also causes strong derepression of the invertase gene SUC2. Deletion of the PP2A subunits Pph21 and Pph22, Rrd1 and Rrd2, specifically enhanced the derepression level of SUC2, indicating that PP2A counteracts SUC2 derepression. Interestingly, the effect of the regulatory subunit Rts1 was consistent with its role as a subunit of both PP2A and PP1, affecting derepression and repression of SUC2, respectively. We also show that abolished phosphatase activation, except by reg1Δ, does not completely block Snf1 dephosphorylation after addition of glucose. Finally, we show that glucose activation of the cAMP-PKA (protein kinase A) pathway is required for glucose activation of both PP2A and PP1. Our results provide novel insight into the complex regulatory role of these two major protein phosphatases in glucose regulation.

Indexed as

beta-FructofuranosidaseCatalytic DomainCyclic AMPCyclic AMP-Dependent Protein KinasesEnzyme ActivationGlucoseIntracellular Signaling Peptides and ProteinsPhosphorylationProtein Phosphatase 1Protein Phosphatase 2Protein Serine-Threonine KinasesSaccharomyces cerevisiaeSaccharomyces cerevisiae Proteinsbeta-FructofuranosidaseCyclic AMPCyclic AMP-Dependent Protein KinasesGLC7 protein, S cerevisiaeGlucoseIntracellular Signaling Peptides and ProteinsPPH21 protein, S cerevisiaeProtein Phosphatase 1Protein Phosphatase 2Protein Serine-Threonine KinasesREG1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSHP1 protein, S cerevisiaeSNF1-related protein kinasesSUC2 protein, S cerevisiae

Identifiers

PMID22290422
PMCPMC3367521
OpenAlexW2005034482

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.