Evidence map›Paper›PMID 24622332›Full record

ArticleG3 (Bethesda, Md.)2014

Coordinated metabolic transitions during Drosophila embryogenesis and the onset of aerobic glycolysis.

Jason M Tennessen, Nicolas M Bertagnolli, Janelle Evans, Matt H Sieber, James Cox, Carl S Thummel

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
3.3field-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

89 citing papers in PubMed, 157 citations in OpenAlex.

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29 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Jason M TennessenDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112 jtenness@indiana.edu.
Nicolas M BertagnolliScientific Computing and Imaging (SCI) Institute, University of Utah, Salt Lake City, Utah 84112 Department of Mathematics, University of Utah, Salt Lake City, Utah 84112.
Janelle EvansDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112.
Matt H SieberDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112.
James CoxDepartment of Biochemistry and the Metabolomics Core Research Facility, University of Utah, Salt Lake City, Utah 84112.
Carl S ThummelDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112.
University of Utah · US

Funding

Regulation and Function of Drosophila Nuclear ReceptorsR01DK075607 · NIDDK · UNIVERSITY OF UTAH · PI THUMMEL, CARL S. · 2006 to 2019
$5.4M
A Drosophila Model for the regulation of Aerobic GlycolysisR00GM101341 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI TENNESSEN, JASON MICHAEL · 2014 to 2016
$739k
A Drosophila Model for the regulation of Aerobic GlycolysisK99GM101341 · NIGMS · UNIVERSITY OF UTAH · PI TENNESSEN, JASON MICHAEL · 2012 to 2013
$180k
NIDDK NIH HHS R01 DK075607NIGMS NIH HHS K99 GM101341NIGMS NIH HHS K99GM101341NIGMS NIH HHS R00 GM101341
6 · The paper itself

Abstract

Rapidly proliferating cells such as cancer cells and embryonic stem cells rely on a specialized metabolic program known as aerobic glycolysis, which supports biomass production from carbohydrates. The fruit fly Drosophila melanogaster also utilizes aerobic glycolysis to support the rapid growth that occurs during larval development. Here we use singular value decomposition analysis of modENCODE RNA-seq data combined with GC-MS-based metabolomic analysis to analyze the changes in gene expression and metabolism that occur during Drosophila embryogenesis, spanning the onset of aerobic glycolysis. Unexpectedly, we find that the most common pattern of co-expressed genes in embryos includes the global switch to glycolytic gene expression that occurs midway through embryogenesis. In contrast to the canonical aerobic glycolytic pathway, however, which is accompanied by reduced mitochondrial oxidative metabolism, the expression of genes involved in the tricarboxylic cycle (TCA cycle) and the electron transport chain are also upregulated at this time. Mitochondrial activity, however, appears to be attenuated, as embryos exhibit a block in the TCA cycle that results in elevated levels of citrate, isocitrate, and α-ketoglutarate. We also find that genes involved in lipid breakdown and β-oxidation are upregulated prior to the transcriptional initiation of glycolysis, but are downregulated before the onset of larval development, revealing coordinated use of lipids and carbohydrates during development. These observations demonstrate the efficient use of nutrient stores to support embryonic development, define sequential metabolic transitions during this stage, and demonstrate striking similarities between the metabolic state of late-stage fly embryos and tumor cells.

Indexed as

MetabolomeAmino AcidsAnimalsCluster AnalysisDrosophilaEmbryonic DevelopmentEnergy MetabolismFatty AcidsFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalGlycolysisMaleMetabolomicsMitochondriaTranscriptional ActivationAmino AcidsFatty Acidstricarballylic acidTricarboxylic Acidsaerobic glycolysisembryogenesismetabolismmetabolomics

Identifiers

PMID24622332
PMCPMC4025483
OpenAlexW2138872672

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.