Evidence map›Paper›PMID 31223645›Full record

ArticleScience advances2019

Reciprocal regulation of TORC signaling and tRNA modifications by Elongator enforces nutrient-dependent cell fate.

Julie Candiracci, Valerie Migeot, Yok-Hian Chionh, Fanelie Bauer, Thomas Brochier, Brandon Russell, Kazuhiro Shiozaki, Peter Dedon, Damien Hermand

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

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  12. The life and times of a tRNA.RNA (New York, N.Y.) · 2023
    Review
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  16. The mTOR signaling pathway in cardiac aging.The journal of cardiovascular aging · 2023
    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

9 authors at 4 institutions in 4 countries.

Julie CandiracciURPHYM-GEMO, University of Namur, rue de Bruxelles, 61, Namur 5000, Belgium.ORCID 0000-0003-3793-7350
Valerie MigeotURPHYM-GEMO, University of Namur, rue de Bruxelles, 61, Namur 5000, Belgium.
Yok-Hian ChionhSingapore-MIT Alliance for Research and Technology Centre (SMART), Center for Life Sciences 05-06, 28 Medical Drive, 117456 Singapore.ORCID 0000-0002-4909-8382
Fanelie BauerURPHYM-GEMO, University of Namur, rue de Bruxelles, 61, Namur 5000, Belgium.ORCID 0000-0002-5887-4806
Thomas BrochierURPHYM-GEMO, University of Namur, rue de Bruxelles, 61, Namur 5000, Belgium.
Brandon RussellMassachusetts Institute of Technology, 56-787B77 Massachusetts Avenue, Cambridge, MA 02139-4307, USA.ORCID 0000-0002-7260-6189
Kazuhiro ShiozakiDivision of Biological Science, Nara Institute of Science and Technology, Ikoma, Nara 630-0192, Japan.ORCID 0000-0002-0395-5457
Peter DedonSingapore-MIT Alliance for Research and Technology Centre (SMART), Center for Life Sciences 05-06, 28 Medical Drive, 117456 Singapore.ORCID 0000-0003-0011-3067
Damien HermandURPHYM-GEMO, University of Namur, rue de Bruxelles, 61, Namur 5000, Belgium.ORCID 0000-0002-1029-5848
University of Namur · BESingapore-MIT Alliance for Research and Technology · SGMassachusetts Institute of Technology · USNara Institute of Science and Technology · JP

Funding

Translational regulation in exposure biology: Xenobiotic-induced reprograming oftRNA modifications and selective translation of codon-biased response genes in rat and humanmodelsR01ES026856 · NIEHS · SUNY POLYTECHNIC INSTITUTE · PI Thomas J Begley, Peter C Dedon · 2016 to 2026
$3.9M
NIEHS NIH HHS R01 ES026856
6 · The paper itself

Abstract

Nutrient availability has a profound impact on cell fate. Upon nitrogen starvation, wild-type fission yeast cells uncouple cell growth from cell division to generate small, round-shaped cells that are competent for sexual differentiation. The TORC1 (TOR complex 1) and TORC2 complexes exert opposite controls on cell growth and cell differentiation, but little is known about how their activity is coordinated. We show that transfer RNA (tRNA) modifications by Elongator are critical for this regulation by promoting the translation of both key components of TORC2 and repressors of TORC1. We further identified the TORC2 pathway as an activator of Elongator by down-regulating a Gsk3 (glycogen synthase kinase 3)-dependent inhibitory phosphorylation of Elongator. Therefore, a feedback control is operating between TOR complex (TORC) signaling and tRNA modification by Elongator to enforce the advancement of mitosis that precedes cell differentiation.

Indexed as

Cell DifferentiationCell ProliferationGene Expression Regulation, FungalGlycogen Synthase Kinase 3Mechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MitosisNutrientsPeptide Chain Elongation, TranslationalPhosphorylationRNA, TransferSchizosaccharomycesSignal TransductionGlycogen Synthase Kinase 3Mechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2NutrientsRNA, Transfer

Identifiers

PMID31223645
PMCPMC6584457
OpenAlexW2951917321

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.