Evidence map›Paper›PMID 25781313›Full record

ArticlePloS one2015

Comparative distribution and in vitro activities of the urotensin II-related peptides URP1 and URP2 in zebrafish: evidence for their colocalization in spinal cerebrospinal fluid-contacting neurons.

Feng B Quan, Christophe Dubessy, Sonya Galant, Natalia B Kenigfest, Lydia Djenoune, Jérôme Leprince, Claire Wyart, Isabelle Lihrmann, Hervé Tostivint

Open access · goldAbstract readComparative Study
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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 61 citations in OpenAlex.

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  12. Zebrafish: an important model for understanding scoliosis.Cellular and molecular life sciences : CMLS · 2022
    Review
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  14. Article
  15. Development of a straight vertebrate body axis.Development (Cambridge, England) · 2020
    Review
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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

9 authors at 7 institutions in 2 countries.

Feng B QuanEvolution des Régulations Endocriniennes, UMR 7221 CNRS, and Muséum National d'Histoire Naturelle, Paris, France.
Christophe DubessyInserm, U982, University of Rouen, Mont-Saint-Aignan, France; Laboratory of Neuronal and Neuroendocrine Differentiation and Communication, Institute for Research and Innovation in Biomedicine (IRIB), University of Rouen, Mont-Saint-Aignan, France; Normandy University, University of Rouen, Mont-Saint-Aignan, France.
Sonya GalantLaboratoire de Neurobiologie et Développement, CNRS UPR 3294, Institut Alfred Fessard, Gif-sur-Yvette, France.
Natalia B KenigfestEvolution des Régulations Endocriniennes, UMR 7221 CNRS, and Muséum National d'Histoire Naturelle, Paris, France; Laboratory of Evolution of Neuronal Interactions, Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia.
Lydia DjenouneEvolution des Régulations Endocriniennes, UMR 7221 CNRS, and Muséum National d'Histoire Naturelle, Paris, France; Institut du Cerveau et de la Moelle épinière, ICM, Inserm U 1127, CNRS, UMR 7225, Sorbonne Universités, UPMC University Paris 06 UMR S 1127, Paris, France.
Jérôme LeprinceInserm, U982, University of Rouen, Mont-Saint-Aignan, France; Laboratory of Neuronal and Neuroendocrine Differentiation and Communication, Institute for Research and Innovation in Biomedicine (IRIB), University of Rouen, Mont-Saint-Aignan, France; Normandy University, University of Rouen, Mont-Saint-Aignan, France.
Claire WyartInstitut du Cerveau et de la Moelle épinière, ICM, Inserm U 1127, CNRS, UMR 7225, Sorbonne Universités, UPMC University Paris 06 UMR S 1127, Paris, France.
Isabelle LihrmannInserm, U982, University of Rouen, Mont-Saint-Aignan, France; Laboratory of Neuronal and Neuroendocrine Differentiation and Communication, Institute for Research and Innovation in Biomedicine (IRIB), University of Rouen, Mont-Saint-Aignan, France; Normandy University, University of Rouen, Mont-Saint-Aignan, France.
Hervé TostivintEvolution des Régulations Endocriniennes, UMR 7221 CNRS, and Muséum National d'Histoire Naturelle, Paris, France.
Inserm · FRCentre National de la Recherche Scientifique · FREvolution des Régulations Endocriniennes · FRInstitute of Evolutionary Physiology and Biochemistry · RULaboratoire de Neurobiologie Cellulaire et Moléculaire · FRSorbonne Université · FRUniversité de Rouen Normandie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Urotensin II (UII) is an evolutionarily conserved neuropeptide initially isolated from teleost fish on the basis of its smooth muscle-contracting activity. Subsequent studies have demonstrated the occurrence of several UII-related peptides (URPs), such that the UII family is now known to include four paralogue genes called UII, URP, URP1 and URP2. These genes probably arose through the two rounds of whole genome duplication that occurred during early vertebrate evolution. URP has been identified both in tetrapods and teleosts. In contrast, URP1 and URP2 have only been observed in ray-finned and cartilaginous fishes, suggesting that both genes were lost in the tetrapod lineage. In the present study, the distribution of urp1 mRNA compared to urp2 mRNA is reported in the central nervous system of zebrafish. In the spinal cord, urp1 and urp2 mRNAs were mainly colocalized in the same cells. These cells were also shown to be GABAergic and express the gene encoding the polycystic kidney disease 2-like 1 (pkd2l1) channel, indicating that they likely correspond to cerebrospinal fluid-contacting neurons. In the hindbrain, urp1-expressing cells were found in the intermediate reticular formation and the glossopharyngeal-vagal motor nerve nuclei. We also showed that synthetic URP1 and URP2 were able to induce intracellular calcium mobilization in human UII receptor (hUT)-transfected CHO cells with similar potencies (pEC50=7.99 and 7.52, respectively) albeit at slightly lower potencies than human UII and mammalian URP (pEC50=9.44 and 8.61, respectively). The functional redundancy of URP1 and URP2 as well as the colocalization of their mRNAs in the spinal cord suggest the robustness of this peptidic system and its physiological importance in zebrafish.

Indexed as

AnimalsCells, CulturedCerebrospinal FluidCHO CellsCricetinaeCricetulusEmbryo, NonmammalianFluorescent Antibody TechniqueHumansIn Situ HybridizationIntracellular Signaling Peptides and ProteinsNeuronsPeptide FragmentsPeptide HormonesReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionIntracellular Signaling Peptides and ProteinsPeptide FragmentsPeptide HormonesRNA, Messengerurotensin IIUrotensinsUTS2B protein, human

Identifiers

PMID25781313
PMCPMC4364556
OpenAlexW2048409720

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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.