Evidence map›Paper›PMID 26856376›Full record

ArticleScientific reports2016

Evolutionary functional elaboration of the Elovl2/5 gene family in chordates.

Óscar Monroig, Mónica Lopes-Marques, Juan C Navarro, Francisco Hontoria, Raquel Ruivo, Miguel M Santos, Byrappa Venkatesh, Douglas R Tocher, L Filipe C Castro

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
13.7field-weighted citation impact, top 1% 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

21 citing papers in PubMed, 83 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

9 authors at 4 institutions in 4 countries.

Óscar MonroigInstitute of Aquaculture, School of Natural Sciences, University of Stirling, Stirling FK9 4LA, Scotland, UK.
Mónica Lopes-MarquesCIIMAR - Interdisciplinary Centre of Marine and Environmental Research, U. Porto - University of Porto, Rua dos Bragas 289, 4050-123 Porto, Portugal.
Juan C NavarroInstituto de Acuicultura Torre de la Sal (IATS-CSIC), Ribera de Cabanes 12595, Castellón, Spain.
Francisco HontoriaInstituto de Acuicultura Torre de la Sal (IATS-CSIC), Ribera de Cabanes 12595, Castellón, Spain.
Raquel RuivoCIIMAR - Interdisciplinary Centre of Marine and Environmental Research, U. Porto - University of Porto, Rua dos Bragas 289, 4050-123 Porto, Portugal.
Miguel M SantosCIIMAR - Interdisciplinary Centre of Marine and Environmental Research, U. Porto - University of Porto, Rua dos Bragas 289, 4050-123 Porto, Portugal.
Byrappa VenkateshInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Biopolis, Singapore 138673.
Douglas R TocherInstitute of Aquaculture, School of Natural Sciences, University of Stirling, Stirling FK9 4LA, Scotland, UK.
L Filipe C CastroCIIMAR - Interdisciplinary Centre of Marine and Environmental Research, U. Porto - University of Porto, Rua dos Bragas 289, 4050-123 Porto, Portugal.
Universidade do Porto · PTInstituto de Acuicultura Torre de la Sal · ESUniversity of Stirling · GBAgency for Science, Technology and Research · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biosynthesis of long-chain polyunsaturated fatty acids (LC-PUFA) provides an intriguing example on how multi-enzymatic cascades evolve. Essential LC-PUFA, such as arachidonic, eicosapentaenoic, and docosahexaenoic acids (DHA), can be acquired from the diet but are also endogenously retailored from C18 precursors through consecutive elongations and desaturations catalyzed, respectively, by fatty acyl elongase and desaturase enzymes. The molecular wiring of this enzymatic pathway defines the ability of a species to biosynthesize LC-PUFA. Exactly when and how in animal evolution a functional LC-PUFA pathway emerged is still elusive. Here we examine key components of the LC-PUFA cascade, the Elovl2/Elovl5 elongases, from amphioxus, an invertebrate chordate, the sea lamprey, a representative of agnathans, and the elephant shark, a basal jawed vertebrate. We show that Elovl2 and Elovl5 emerged from genome duplications in vertebrate ancestry. The single Elovl2/5 from amphioxus efficiently elongates C18 and C20 and, to a marked lesser extent, C22 LC-PUFA. Lamprey is incapable of elongating C22 substrates. The elephant shark Elovl2 showed that the ability to efficiently elongate C22 PUFA and thus to synthesize DHA through the Sprecher pathway, emerged in the jawed vertebrate ancestor. Our findings illustrate how non-integrated "metabolic islands" evolve into fully wired pathways upon duplication and neofunctionalization.

Indexed as

Evolution, MolecularAcetyltransferasesAnimalsFish ProteinsGene DuplicationLampreysLanceletsSharksAcetyltransferasesFish Proteins

Identifiers

PMID26856376
PMCPMC4746653
OpenAlexW2274235422

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.