Evidence map›Paper›PMID 26356221›Full record

ArticlePloS one2015

The Unc-5 Receptor Is Directly Regulated by Tinman in the Developing Drosophila Dorsal Vessel.

Jamshid Asadzadeh, Niamh Neligan, Judith J Canabal-Alvear, Amanda C Daly, Sunita Gupta Kramer, Juan-Pablo Labrador

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Genome-Wide Approaches to Drosophila Heart Development.Journal of cardiovascular development and disease · 2016
    Article
  2. Article
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 2 institutions in 2 countries.

Jamshid AsadzadehSmurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland; Institute of Neuroscience, Trinity College Dublin, Dublin, Ireland.
Niamh NeliganSmurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.
Judith J Canabal-AlvearDepartment of Pathology and Laboratory Medicine, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.
Amanda C DalySmurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland; Institute of Neuroscience, Trinity College Dublin, Dublin, Ireland.
Sunita Gupta KramerDepartment of Pathology and Laboratory Medicine, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.
Juan-Pablo LabradorSmurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland; Institute of Neuroscience, Trinity College Dublin, Dublin, Ireland.
Trinity College Dublin · IERutgers, The State University of New Jersey · US

Funding

UMDNJ-RUTGERS UNIVERSITY PIPELINE PROGRAMR25GM055145 · NIGMS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI HAIMOVICH, BEATRICE, LANGER, JEROME ALAN · 1996 to 2020
$8.7M
6 · The paper itself

Abstract

During early heart morphogenesis cardiac cells migrate in two bilateral opposing rows, meet at the dorsal midline and fuse to form a hollow tube known as the primary heart field in vertebrates or dorsal vessel (DV) in Drosophila. Guidance receptors are thought to mediate this evolutionarily conserved process. A core of transcription factors from the NK2, GATA and T-box families are also believed to orchestrate this process in both vertebrates and invertebrates. Nevertheless, whether they accomplish their function, at least in part, through direct or indirect transcriptional regulation of guidance receptors is currently unknown. In our work, we demonstrate how Tinman (Tin), the Drosophila homolog of the Nkx-2.5 transcription factor, regulates the Unc-5 receptor during DV tube morphogenesis. We use genetics, expression analysis with single cell mRNA resolution and enhancer-reporter assays in vitro or in vivo to demonstrate that Tin is required for Unc-5 receptor expression specifically in cardioblasts. We show that Tin can bind to evolutionary conserved sites within an Unc-5 DV enhancer and that these sites are required for Tin-dependent transactivation both in vitro and in vivo.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBase SequenceBinding SitesDrosophilaDrosophila ProteinsEnhancer Elements, GeneticGene ExpressionGenes, ReporterHeartMyoblasts, CardiacNucleotide MotifsProtein BindingRepressor ProteinsSequence AlignmentTrans-ActivatorsDrosophila ProteinsRepressor Proteinstin protein, DrosophilaTrans-Activators

Identifiers

PMID26356221
PMCPMC4565662
OpenAlexW2206642044

What OpenQuestion holds

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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.