Evidence map›Paper›PMID 18454855›Full record

ArticleBMC evolutionary biology2008

The metazoan history of the COE transcription factors. Selection of a variant HLH motif by mandatory inclusion of a duplicated exon in vertebrates.

Virginie Daburon, Sébastien Mella, Jean-Louis Plouhinec, Sylvie Mazan, Michèle Crozatier, Alain Vincent

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In one paragraph

Article in BMC evolutionary biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 32 citations in OpenAlex.

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  5. De novo variants inCold Spring Harbor molecular case studies · 2017
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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Virginie DaburonCentre de Biologie du Développement, UMR 5547 and IFR 109 CNRS/UPS, 118 route de Narbonne 31062 Toulouse cedex 4, France. daburon@cict.fr
Sébastien Mella
Jean-Louis Plouhinec
Sylvie Mazan
Michèle Crozatier
Alain Vincent
Université Toulouse III - Paul Sabatier · FRCentre de Biologie du Développement · FRCentre National de la Recherche Scientifique · FRHoward Hughes Medical Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing number of available genomic sequences makes it now possible to study the evolutionary history of specific genes or gene families. Transcription factors (TFs) involved in regulation of gene-specific expression are key players in the evolution of metazoan development. The low complexity COE (Collier/Olfactory-1/Early B-Cell Factor) family of transcription factors constitutes a well-suited paradigm for studying evolution of TF structure and function, including the specific question of protein modularity. Here, we compare the structure of coe genes within the metazoan kingdom and report on the mechanism behind a vertebrate-specific exon duplication.

resultsCOE proteins display a modular organisation, with three highly conserved domains : a COE-specific DNA-binding domain (DBD), an Immunoglobulin/Plexin/transcription (IPT) domain and an atypical Helix-Loop-Helix (HLH) motif. Comparison of the splice structure of coe genes between cnidariae and bilateriae shows that the ancestral COE DBD was built from 7 separate exons, with no evidence for exon shuffling with other metazoan gene families. It also confirms the presence of an ancestral H1LH2 motif present in all COE proteins which partly overlaps the repeated H2d-H2a motif first identified in rodent EBF. Electrophoretic Mobility Shift Assays show that formation of COE dimers is mediated by this ancestral motif. The H2d-H2a alpha-helical repetition appears to be a vertebrate characteristic that originated from a tandem exon duplication having taken place prior to the splitting between gnathostomes and cyclostomes. We put-forward a two-step model for the inclusion of this exon in the vertebrate transcripts.

conclusionThree main features in the history of the coe gene family can be inferred from these analyses: (i) each conserved domain of the ancestral coe gene was built from multiple exons and the same scattered structure has been maintained throughout metazoan evolution. (ii) There exists a single coe gene copy per metazoan genome except in vertebrates. The H2a-H2d duplication that is specific to vertebrate proteins provides an example of a novel vertebrate characteristic, which may have been fixed early in the gnathostome lineage. (iii) This duplication provides an interesting example of counter-selection of alternative splicing.

Indexed as

Evolution, MolecularAmino Acid SequenceAnimalsBasic Helix-Loop-Helix ProteinsBayes TheoremDrosophilaExonsHelix-Loop-Helix MotifsPhylogenySequence AlignmentTranscription FactorsVertebratesBasic Helix-Loop-Helix ProteinsTranscription Factors

Identifiers

PMID18454855
PMCPMC2394523
OpenAlexW2112520791

What OpenQuestion holds

Textmetadata
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.