Evidence map›Paper›PMID 25984292›Full record

ArticleEvoDevo2015

Evolution of retinoic acid receptors in chordates: insights from three lamprey species, Lampetra fluviatilis, Petromyzon marinus, and Lethenteron japonicum.

Florent Campo-Paysaa, David Jandzik, Yoko Takio-Ogawa, Maria V Cattell, Haley C Neef, James A Langeland, Shigeru Kuratani, Daniel M Medeiros, Sylvie Mazan, Shigehiro Kuraku and 2 more

Open access · goldAbstract read
In one paragraph

Article in EvoDevo, 2015. 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
1.0field-weighted citation impact, top 20% 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, 26 citations in OpenAlex.

  1. Review
  2. Article
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  4. 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

12 authors at 6 institutions in 3 countries.

Florent Campo-PaysaaMolecular Zoology Team, Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69364 Lyon Cedex 07, France ; MRC Centre for Developmental Neurobiology, New Hunt's House, King's College London, Guy's Campus, London, SE1 1UL UK.
David JandzikDepartment of Ecology and Evolutionary Biology, University of Colorado Boulder, Ramaley Biology, 1800 Colorado Avenue, Boulder, CO 80309 USA ; Department of Zoology, Comenius University in Bratislava, Mlynska Dolina B-1, 84215 Bratislava, Slovakia.
Yoko Takio-OgawaLaboratory for Evolutionary Morphology, RIKEN, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047 Japan.
Maria V CattellDepartment of Ecology and Evolutionary Biology, University of Colorado Boulder, Ramaley Biology, 1800 Colorado Avenue, Boulder, CO 80309 USA ; Department of Pediatrics, University of Colorado, Children's Hospital, 13065 East 17th Avenue, Aurora, CO 80045 USA.
Haley C NeefDepartment of Biology, Kalamazoo College, 1200 Academy Street, Kalamazoo, Michigan 49008 USA ; Division of Pediatric Gastroenterology, Department of Pediatrics and Communicable Diseases, University of Michigan, C.S. Mott Children's Hospital, 1540 East Hospital Drive SPC 4259, Ann Arbor, Michigan 48109 USA.
James A LangelandDepartment of Biology, Kalamazoo College, 1200 Academy Street, Kalamazoo, Michigan 49008 USA.
Shigeru KurataniLaboratory for Evolutionary Morphology, RIKEN, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047 Japan.
Daniel M MedeirosDepartment of Ecology and Evolutionary Biology, University of Colorado Boulder, Ramaley Biology, 1800 Colorado Avenue, Boulder, CO 80309 USA.
Sylvie MazanSorbonne Universités, UPMC Université Paris 06, FR2424, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France ; CNRS, FR2424, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France.
Shigehiro KurakuGenome Resource and Analysis Unit, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047 Japan ; Phyloinformatics Unit, RIKEN Center for Life Science Technologies, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047 Japan.
Vincent LaudetMolecular Zoology Team, Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon, 69364 Lyon Cedex 07, France.
Michael SchubertSorbonne Universités, UPMC Université Paris 06, UMR 7009, Laboratoire de Biologie du Développement de Villefranche-sur-Mer, Observatoire Océanologique de Villefranche-sur-Mer, 181 Chemin du Lazaret, 06230 Villefranche-sur-Mer, France ; CNRS, UMR 7009, Laboratoire de Biologie du Développement de Villefranche-sur-Mer, Observatoire Océanologique de Villefranche-sur-Mer, 181 Chemin du Lazaret, 06230 Villefranche-sur-Mer, France.
University of Colorado Boulder · USKalamazoo College · USUniversité Claude Bernard Lyon 1 · FRRIKEN Center for Computational Science · JPSorbonne Université · FRStation Biologique de Roscoff · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRetinoic acid (RA) signaling controls many developmental processes in chordates, from early axis specification to late organogenesis. The functions of RA are chiefly mediated by a subfamily of nuclear hormone receptors, the retinoic acid receptors (RARs), that act as ligand-activated transcription factors. While RARs have been extensively studied in jawed vertebrates (that is, gnathostomes) and invertebrate chordates, very little is known about the repertoire and developmental roles of RARs in cyclostomes, which are extant jawless vertebrates. Here, we present the first extensive study of cyclostome RARs focusing on three different lamprey species: the European freshwater lamprey, Lampetra fluviatilis, the sea lamprey, Petromyzon marinus, and the Japanese lamprey, Lethenteron japonicum.

resultsWe identified four rar paralogs (rar1, rar2, rar3, and rar4) in each of the three lamprey species, and phylogenetic analyses indicate a complex evolutionary history of lamprey rar genes including the origin of rar1 and rar4 by lineage-specific duplication after the lamprey-hagfish split. We further assessed their expression patterns during embryonic development by in situ hybridization. The results show that lamprey rar genes are generally characterized by dynamic and highly specific expression domains in different embryonic tissues. In particular, lamprey rar genes exhibit combinatorial expression domains in the anterior central nervous system (CNS) and the pharyngeal region.

conclusionsOur results indicate that the genome of lampreys encodes at least four rar genes and suggest that the lamprey rar complement arose from vertebrate-specific whole genome duplications followed by a lamprey-specific duplication event. Moreover, we describe a combinatorial code of lamprey rar expression in both anterior CNS and pharynx resulting from dynamic and highly specific expression patterns during embryonic development. This 'RAR code' might function in regionalization and patterning of these two tissues by differentially modulating the expression of downstream effector genes during development.

Indexed as

AgnathanCyclostomeDevelopmental patterningGene duplicationGnathostomeRAR codeRetinoid signalingVertebrate

Identifiers

PMID25984292
PMCPMC4432984
OpenAlexW2131424912

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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.