Evidence map›Paper›PMID 26994946›Full record

ArticleDevelopmental biology2016

Gia/Mthl5 is an aorta specific GPCR required for Drosophila heart tube morphology and normal pericardial cell positioning.

Meghna V Patel, Jun-Yi Zhu, Zhiping Jiang, Adam Richman, Mark F A VanBerkum, Zhe Han

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  4. Cytokine signaling throughProceedings of the National Academy of Sciences of the United States of America · 2017
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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

6 authors at 2 institutions in 1 country.

Meghna V PatelDepartment of Biological Sciences, Wayne State University, 5047 Gullen Mall, Detroit, MI 48202, USA.
Jun-Yi ZhuCenter for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, 111 Michigan Ave. NW, Washington, DC 20010, USA.
Zhiping JiangCenter for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, 111 Michigan Ave. NW, Washington, DC 20010, USA.
Adam RichmanCenter for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, 111 Michigan Ave. NW, Washington, DC 20010, USA.
Mark F A VanBerkumDepartment of Biological Sciences, Wayne State University, 5047 Gullen Mall, Detroit, MI 48202, USA.
Zhe HanCenter for Cancer and Immunology Research, Children's Research Institute, Children's National Medical Center, 111 Michigan Ave. NW, Washington, DC 20010, USA. Electronic address: ZHan@childrensnational.org.
Children's National · USWayne State University · US

Funding

Modeling Nephrotic Syndrome in Drosophila NephrocytesR01DK098410 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HAN, ZHE · 2014 to 2022
$3.3M
A novel G protein signaling pathway controlling Drosophila cardiac morphogenesisR01HL090801 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HAN, ZHE · 2008 to 2012
$2.0M
NHLBI NIH HHS R01 HL090801NIDDK NIH HHS R01 DK098410
6 · The paper itself

Abstract

G-protein signaling is known to be required for cell-cell contacts during the development of the Drosophila dorsal vessel. However, the identity of the G protein-coupled receptor (GPCR) that regulates this signaling pathway activity is unknown. Here we describe the identification of a novel cardiac specific GPCR, called Gia, for "GPCR in aorta". Gia is the only heart-specific GPCR identified in Drosophila to date and it is specifically expressed in cardioblasts that fuse at the dorsal midline to become the aorta. Gia is the only Drosophila gene so far identified for which expression is entirely restricted to cells of the aorta. Deletion of Gia led to a broken-hearted phenotype, characterized by pericardial cells dissociated from cardioblasts and abnormal distribution of cell junction proteins. Both phenotypes were similar to those observed in mutants of the heterotrimeric cardiac G proteins. Lack of Gia also led to defects in the alignment and fusion of cardioblasts in the aorta. Gia forms a protein complex with G-αo47A, the alpha subunit of the heterotrimeric cardiac G proteins and interacts genetically with G-αo47A during cardiac morphogenesis. Our study identified Gia as an essential aorta-specific GPCR that functions upstream of cardiac heterotrimeric G proteins and is required for morphological integrity of the aorta during heart tube formation. These studies lead to a redefinition of the bro phenotype, to encompass morphological integrity of the heart tube as well as cardioblast-pericardial cell spatial interactions.

Indexed as

AnimalsAnimals, Genetically ModifiedAortaDrosophila melanogasterDrosophila ProteinsGene DeletionGene Expression Regulation, DevelopmentalGenes, LethalHeartMorphogenesisPericardiumPhenotypeProtein Interaction MappingReceptors, G-Protein-CoupledRecombinant Fusion ProteinsDrosophila ProteinsMthl5 protein, DrosophilaReceptors, G-Protein-CoupledRecombinant Fusion ProteinsDrosophilaGiaG protein coupled receptorHeart developmentMethuselah-like

Identifiers

PMID26994946
PMCPMC4875858
OpenAlexW2300048757

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Registered trials

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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.