Evidence map›Paper›PMID 25093834›Full record

ArticlePloS one2014

Wnt pathway activation increases hypoxia tolerance during development.

Merril Gersten, Dan Zhou, Priti Azad, Gabriel G Haddad, Shankar Subramaniam

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  5. Article
  6. A Screening of UNF Targets IdentifiesThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    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

5 authors at 1 institution in 1 country.

Merril GerstenBioinformatics and Systems Biology Graduate Program, University of California San Diego, La Jolla, California, United States of America.
Dan ZhouDepartment of Pediatrics, University of California San Diego, La Jolla, California, United States of America.
Priti AzadDepartment of Pediatrics, University of California San Diego, La Jolla, California, United States of America.
Gabriel G HaddadDepartment of Pediatrics, University of California San Diego, La Jolla, California, United States of America; Department of Neuroscience, University of California San Diego, La Jolla, California, United States of America; Rady Children's Hospital, San Diego, California, United States of America.
Shankar SubramaniamBioinformatics and Systems Biology Graduate Program, University of California San Diego, La Jolla, California, United States of America; Department of Bioengineering, University of California San Diego, La Jolla, California, United States of America; Departments of Cellular and Molecular Medicine, Chemistry and Biochemistry and Nanoengineering, University of California San Diego, La Jolla, California, United States of America.
University of California, San Diego · US

Funding

THE IMPACT OF HYPOXIA ON DEVELOPMENT AND REMODELING OF CARDIC INTERCALATED DISKP01HD032573 · NICHD · YALE UNIVERSITY · PI HADDAD, GABRIEL G · 1995 to 2009
$12.1M
Systems Biology CoreP01HL098053 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI POWELL, FRANK L. · 2010 to 2014
$10.2M
MOLECULAR BASIS OF CELL TOLERANCE TO 02 DEPRIVATIONR01NS037756 · NINDS · YESHIVA UNIVERSITY · PI HADDAD, GABRIEL G · 2000 to 2009
$4.1M
Signaling GatewayR01GM078005 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2006 to 2012
$3.7M
Reconstruction and Modeling of Networks Involved in Cardiomyoctye DifferentiationR33HL087375 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SUBRAMANIAM, SHANKAR · 2007 to 2009
$1.1M
NHLBI NIH HHS 1P01HL098053NHLBI NIH HHS 5 R33 HL087375-02NHLBI NIH HHS P01 HL098053NHLBI NIH HHS R33 HL087375NICHD NIH HHS 5P01HD032573NICHD NIH HHS P01 HD032573NIGMS NIH HHS GM078005-05NIGMS NIH HHS R01 GM078005NINDS NIH HHS 5R01NS037756NINDS NIH HHS R01 NS037756
6 · The paper itself

Abstract

Adaptation to hypoxia, defined as a condition of inadequate oxygen supply, has enabled humans to successfully colonize high altitude regions. The mechanisms attempted by organisms to cope with short-term hypoxia include increased ATP production via anaerobic respiration and stabilization of Hypoxia Inducible Factor 1α (HIF-1α). However, less is known about the means through which populations adapt to chronic hypoxia during the process of development within a life time or over generations. Here we show that signaling via the highly conserved Wnt pathway impacts the ability of Drosophila melanogaster to complete its life cycle under hypoxia. We identify this pathway through analyses of genome sequencing and gene expression of a Drosophila melanogaster population adapted over >180 generations to tolerate a concentration of 3.5-4% O2 in air. We then show that genetic activation of the Wnt canonical pathway leads to increased rates of adult eclosion in low O2. Our results indicate that a previously unsuspected major developmental pathway, Wnt, plays a significant role in hypoxia tolerance.

Indexed as

Drosophila melanogasterWnt Signaling PathwayAdaptation, PhysiologicalAnimalsEmbryonic DevelopmentEmbryo, NonmammalianGene Expression Regulation, DevelopmentalGrowth and DevelopmentHypoxiaOxygenPolymorphism, Single NucleotideOxygen

Identifiers

PMID25093834
PMCPMC4122365
OpenAlexW1964292463

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.