Evidence map›Paper›PMID 27066235›Full record

ArticleEcology and evolution2016

Diversification and coevolution of the ghrelin/growth hormone secretagogue receptor system in vertebrates.

Mbaye Tine, Heiner Kuhl, Peter R Teske, Matthias H Tschöp, Martin Jastroch

Open access · goldAbstract read
In one paragraph

Article in Ecology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

5 citing papers in PubMed, 19 citations in OpenAlex.

  1. Genetic Differences in Purple Finch (Ecology and evolution · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Ghrelin-Mediated Regeneration and Plasticity After Nervous System Injury.Frontiers in cell and developmental biology · 2021
    Review
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 4 institutions in 2 countries.

Mbaye TineGenome Centre at Max Planck Institute for Plant Breeding Research Carl-von-Linné-Weg 10D-50829 Köln Germany; Molecular Zoology Laboratory Department of Zoology University of Johannesburg Kingsway Campus Auckland Park 2006 South Africa.
Heiner KuhlMax Planck Institute for Molecular Genetics Ihnestrasse 63-73 14195 Berlin Germany.
Peter R TeskeMolecular Zoology Laboratory Department of Zoology University of Johannesburg Kingsway Campus Auckland Park 2006 South Africa.
Matthias H TschöpHelmholtz Diabetes Center & German Diabetes Center (DZD) Helmholtz Zentrum München, 85764 Neuherberg, Germany; Division of Metabolic Diseases Technische Universität München 80333 Munich Germany.
Martin JastrochHelmholtz Diabetes Center & German Diabetes Center (DZD) Helmholtz Zentrum München, 85764 Neuherberg, Germany; Division of Metabolic Diseases Technische Universität München 80333 Munich Germany.
Helmholtz Zentrum München · DEMax Planck Institute for Molecular Genetics · DEMax Planck Institute for Plant Breeding Research · DEUniversity of Johannesburg · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut hormone ghrelin is involved in numerous metabolic functions, such as the stimulation of growth hormone secretion, gastric motility, and food intake. Ghrelin is modified by ghrelin O-acyltransferase (GOAT) or membrane-bound O-acyltransferase domain-containing 4 (MBOAT4) enabling action through the growth hormone secretagogue receptors (GHS-R). During the course of evolution, initially strong ligand/receptor specificities can be disrupted by genomic changes, potentially modifying physiological roles of the ligand/receptor system. Here, we investigated the coevolution of ghrelin, GOAT, and GHS-R in vertebrates. We combined similarity search, conserved synteny analyses, phylogenetic reconstructions, and protein structure comparisons to reconstruct the evolutionary history of the ghrelin system. Ghrelin remained a single-gene locus in all vertebrate species, and accordingly, a single GHS-R isoform was identified in all tetrapods. Similar patterns of the nonsynonymous (dN) and synonymous (dS) ratio (dN/dS) in the vertebrate lineage strongly suggest coevolution of the ghrelin and GHS-R genes, supporting specific functional interactions and common physiological pathways. The selection profiles do not allow confirmation as to whether ghrelin binds specifically to GOAT, but the ghrelin dN/dS patterns are more similar to those of GOAT compared to MBOAT1 and MBOAT2 isoforms. Four GHS-R isoforms were identified in teleost genomes. This diversification of GHS-R resulted from successive rounds of duplications, some of which remained specific to the teleost lineage. Coevolution signals are lost in teleosts, presumably due to the diversification of GHS-R but not the ghrelin gene. The identification of the GHS-R diversity in teleosts provides a molecular basis for comparative studies on ghrelin's physiological roles and regulation, while the comparative sequence and structure analyses will assist translational medicine to determine structure-function relationships of the ghrelin/GHS-R system.

Indexed as

Coevolutiondivergencefunctionghrelingrowth hormone secretagogue receptorvertebrates

Identifiers

PMID27066235
PMCPMC4797157
OpenAlexW2303652498

What OpenQuestion holds

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LicenceCC BY
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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.