Evidence map›Paper›PMID 33244091›Full record

ArticleScientific reports2020

An improved de novo assembling and polishing of Solea senegalensis transcriptome shed light on retinoic acid signalling in larvae.

José Córdoba-Caballero, Pedro Seoane, Fernando M Jabato, James R Perkins, Manuel Manchado, M Gonzalo Claros

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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
0.7field-weighted citation impact, top 27% 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, 10 citations in OpenAlex.

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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 4 institutions in 1 country.

José Córdoba-CaballeroDepartment of Molecular Biology and Biochemistry, Universidad de Málaga, Málaga, 29071, Spain.
Pedro SeoaneDepartment of Molecular Biology and Biochemistry, Universidad de Málaga, Málaga, 29071, Spain.
Fernando M JabatoDepartment of Molecular Biology and Biochemistry, Universidad de Málaga, Málaga, 29071, Spain.
James R PerkinsDepartment of Molecular Biology and Biochemistry, Universidad de Málaga, Málaga, 29071, Spain.
Manuel ManchadoConsejería de Agricultura, Ganadería, Pesca y Desarrollo Sostenible, IFAPA Centro El Toruño, El Puerto de Santa María, Cádiz, 11500, Spain.
M Gonzalo ClarosDepartment of Molecular Biology and Biochemistry, Universidad de Málaga, Málaga, 29071, Spain. claros@uma.es.
Instituto de Investigación de Enfermedades Raras · ESUniversidad de Málaga · ESAndalusian Institute of Agricultural and Fisheries Research and Training · ESCentre for Biomedical Network Research on Rare Diseases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Senegalese sole is an economically important flatfish species in aquaculture and an attractive model to decipher the molecular mechanisms governing the severe transformations occurring during metamorphosis, where retinoic acid seems to play a key role in tissue remodeling. In this study, a robust sole transcriptome was envisaged by reducing the number of assembled libraries (27 out of 111 available), fine-tuning a new automated and reproducible set of workflows for de novo assembling based on several assemblers, and removing low confidence transcripts after mapping onto a sole female genome draft. From a total of 96 resulting assemblies, two "raw" transcriptomes, one containing only Illumina reads and another with Illumina and GS-FLX reads, were selected to provide SOLSEv5.0, the most informative transcriptome with low redundancy and devoid of most single-exon transcripts. It included both Illumina and GS-FLX reads and consisted of 51,348 transcripts of which 22,684 code for 17,429 different proteins described in databases, where 9527 were predicted as complete proteins. SOLSEv5.0 was used as reference for the study of retinoic acid (RA) signalling in sole larvae using drug treatments (DEAB, a RA synthesis blocker, and TTNPB, a RA-receptor agonist) for 24 and 48 h. Differential expression and functional interpretation were facilitated by an updated version of DEGenes Hunter. Acute exposure of both drugs triggered an intense, specific and transient response at 24 h but with hardly observable differences after 48 h at least in the DEAB treatments. Activation of RA signalling by TTNPB specifically increased the expression of genes in pathways related to RA degradation, retinol storage, carotenoid metabolism, homeostatic response and visual cycle, and also modified the expression of transcripts related to morphogenesis and collagen fibril organisation. In contrast, DEAB mainly decreased genes related to retinal production, impairing phototransduction signalling in the retina. A total of 755 transcripts mainly related to lipid metabolism, lipid transport and lipid homeostasis were altered in response to both treatments, indicating non-specific drug responses associated with intestinal absorption. These results indicate that a new assembling and transcript sieving were both necessary to provide a reliable transcriptome to identify the many aspects of RA action during sole development that are of relevance for sole aquaculture.

Indexed as

AnimalsBenzoatesCarotenoidsCollagenFemaleFlatfishesGenomeHomeostasisLarvaLipid MetabolismMetamorphosis, BiologicalMorphogenesisReceptors, Retinoic AcidRetinaRetinoidsSignal Transduction4-(2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1-propenyl)benzoic acidBenzoatesCarotenoidsCollagenReceptors, Retinoic AcidRetinoidsTretinoin

Identifiers

PMID33244091
PMCPMC7691524
OpenAlexW3108888485

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LicenceCC BY
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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.