Evidence map›Paper›PMID 20089194›Full record

ArticleBMC cell biology2010

Nutritional control of gene expression in Drosophila larvae via TOR, Myc and a novel cis-regulatory element.

Ling Li, Bruce A Edgar, Savraj S Grewal

Open access · goldAbstract read
In one paragraph

Article in BMC cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.5field-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

44 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
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  10. Genes & nutrition · 2019
    Review
  11. Evolutionary responses ofFrontiers in ecology and evolution · 2018
    Article
  12. Review
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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

3 authors at 2 institutions in 2 countries.

Ling LiClark H, Smith Brain Tumour Center, Southern Alberta Cancer Research Institute, Calgary, Alberta T2N 4N1, Canada.
Bruce A Edgar
Savraj S Grewal
Fred Hutch Cancer Center · USAlberta Cancer Foundation · CA

Funding

Canadian Institutes of Health ResearchNIGMS NIH HHS GM51186
6 · The paper itself

Abstract

backgroundNutrient availability is a key determinant of eukaryotic cell growth. In unicellular organisms many signaling and transcriptional networks link nutrient availability to the expression of metabolic genes required for growth. However, less is known about the corresponding mechanisms that operate in metazoans. We used gene expression profiling to explore this issue in developing Drosophila larvae.

resultsWe found that starvation for dietary amino acids (AA's) leads to dynamic changes in transcript levels of many metabolic genes. The conserved insulin/PI3K and TOR signaling pathways mediate nutrition-dependent growth in Drosophila and other animals. We found that many AA starvation-responsive transcripts were also altered in TOR mutants. In contrast, although PI3K overexpression induced robust changes in the expression of many metabolic genes, these changes showed limited overlap with the AA starvation expression profile. We did however identify a strong overlap between genes regulated by the transcription factor, Myc, and AA starvation-responsive genes, particularly those involved in ribosome biogenesis, protein synthesis and mitochondrial function. The consensus Myc DNA binding site is enriched in promoters of these AA starvation genes, and we found that Myc overexpression could bypass dietary AA to induce expression of these genes. We also identified another sequence motif (Motif 1) enriched in the promoters of AA starvation-responsive genes. We showed that Motif 1 was both necessary and sufficient to mediate transcriptional responses to dietary AA in larvae.

conclusionsOur data suggest that many of the transcriptional effects of amino acids are mediated via signaling through the TOR pathway in Drosophila larvae. We also find that these transcriptional effects are mediated through at least two mechanisms: via the transcription factor Myc, and via the Motif 1 cis-regulatory element. These studies begin to elucidate a nutrient-responsive signaling network that controls metabolic gene transcription in Drosophila.

Indexed as

Gene Expression RegulationAmino AcidsAnimalsDietDrosophilaDrosophila ProteinsGene Expression ProfilingLarvaMicroarray AnalysisPhosphatidylinositol 3-KinasesPromoter Regions, GeneticProto-Oncogene Proteins c-mycReceptor Protein-Tyrosine KinasesSignal TransductionAmino AcidsDrosophila ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-mycReceptor Protein-Tyrosine Kinasestor protein, Drosophila

Identifiers

PMID20089194
PMCPMC2827378
OpenAlexW2149049981

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.