Evidence map›Paper›PMID 27255611›Full record

ArticleScientific reports2016

Nutrient shortage triggers the hexosamine biosynthetic pathway via the GCN2-ATF4 signalling pathway.

Cédric Chaveroux, Carmen Sarcinelli, Virginie Barbet, Sofiane Belfeki, Audrey Barthelaix, Carole Ferraro-Peyret, Serge Lebecque, Toufic Renno, Alain Bruhat, Pierre Fafournoux and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

54 citing papers in PubMed, 73 citations in OpenAlex.

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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

11 authors at 8 institutions in 1 country.

Cédric ChaverouxINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Carmen SarcinelliINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Virginie BarbetINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Sofiane BelfekiINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Audrey BarthelaixINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Carole Ferraro-PeyretINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Serge LebecqueINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Toufic RennoINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Alain BruhatINRA, UMR 1019 Nutrition Humaine, Centre de Clermont-Ferrand-Theix, 63122 Saint Genès Champanelle, France.
Pierre FafournouxINRA, UMR 1019 Nutrition Humaine, Centre de Clermont-Ferrand-Theix, 63122 Saint Genès Champanelle, France.
Serge N ManiéINSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, F-69000 Lyon, France.
Centre de Recherche en Cancérologie de Lyon · FRCentre Léon Bérard · FRInserm · FRCentre de Recherche en Cancérologie de Marseille · FRCentre de Recherche en Nutrition Humaine d'Auvergne · FRCentre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRUniversité Clermont Auvergne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hexosamine biosynthetic pathway (HBP) is a nutrient-sensing metabolic pathway that produces the activated amino sugar UDP-N-acetylglucosamine, a critical substrate for protein glycosylation. Despite its biological significance, little is known about the regulation of HBP flux during nutrient limitation. Here, we report that amino acid or glucose shortage increase GFAT1 production, the first and rate-limiting enzyme of the HBP. GFAT1 is a transcriptional target of the activating transcription factor 4 (ATF4) induced by the GCN2-eIF2α signalling pathway. The increased production of GFAT1 stimulates HBP flux and results in an increase in O-linked β-N-acetylglucosamine protein modifications. Taken together, these findings demonstrate that ATF4 provides a link between nutritional stress and the HBP for the regulation of the O-GlcNAcylation-dependent cellular signalling.

Indexed as

AcetylglucosamineActivating Transcription Factor 4Amino AcidsAnimalsBiosynthetic PathwaysCell LineGlucoseHeLa CellsHexosaminesHumansMiceNitrogenous Group TransferasesProtein Serine-Threonine KinasesRatsSignal TransductionAcetylglucosamineActivating Transcription Factor 4Amino AcidsGlucoseHexosaminesNitrogenous Group TransferasesProtein Serine-Threonine Kinases

Identifiers

PMID27255611
PMCPMC4891703
OpenAlexW2413679979

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.