Evidence map›Paper›PMID 18715504›Full record

ArticleBMC genomics2008

Rapid functional diversification in the structurally conserved ELAV family of neuronal RNA binding proteins.

Marie-Laure Samson

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. The Evolution of Bees: Insights from 'Omic Studies.Genome biology and evolution · 2026
    Review
  2. Article
  3. Article
  4. The molecular genetics of nELAVL in brain development and disease.European journal of human genetics : EJHG · 2023
    Review
  5. Article
  6. Review
  7. Alterations of RNA-binding proteinFrontiers in molecular neuroscience · 2022
    Article
  8. Article
  9. Article
  10. Unlike Drosophila elav, themicroPublication biology · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. 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

1 author at 1 institution in 1 country.

Marie-Laure SamsonLaboratoire Signalisation, Développement et Cancer, UMR8080 Développement et Evolution, CNRS and Université Paris Sud, Bâtiment 442 bis, 91405, Orsay Cedex, France. Marie-Laure.Samson@u-psud.fr
Université Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Drosophila gene embryonic lethal abnormal visual system (elav) is the prototype of a gene family present in all metazoans. Its members encode structurally conserved neuronal proteins with three RNA Recognition Motifs (RRM) but they paradoxically act at diverse levels of post-transcriptional regulation. In an attempt to understand the history of this family, we searched for orthologs in eleven completely sequenced genomes, including those of humans, D. melanogaster and C. elegans, for which cDNAs are available.

resultsWe analyzed 23 orthologs/paralogs of elav, and found evidence of gain/loss of gene copy number. For one set of genes, including elav itself, the coding sequences are free of introns and their products most resemble ELAV. The remaining genes show remarkable conservation of their exon organization, and their products most resemble FNE and RBP9, proteins encoded by the two elav paralogs of Drosophila. Remarkably, three of the conserved exon junctions are both close to structural elements, involved respectively in protein-RNA interactions and in the regulation of sub-cellular localization, and in the vicinity of diverse sequence variations.

conclusionThe data indicate that the essential elav gene of Drosophila is newly emerged, restricted to dipterans and of retrotransposed origin. We propose that the conserved exon junctions constitute potential sites for sequence/function modifications, and that RRM binding proteins, whose function relies upon plastic RNA-protein interactions, may have played an important role in brain evolution.

Indexed as

Conserved SequenceMultigene FamilyAmino Acid SequenceAnimalsCaenorhabditis elegansDrosophila melanogasterDrosophila ProteinsELAV ProteinsEvolution, MolecularExonsGene DosageGene Expression RegulationHumansMolecular Sequence DataNerve Tissue ProteinsPhylogenyDrosophila ProteinsELAV protein, DrosophilaELAV ProteinsNerve Tissue Proteins

Identifiers

PMID18715504
PMCPMC2529313
OpenAlexW2118228813

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.