Evidence map›Paper›PMID 27588814›Full record

ArticlePLoS genetics2016

Evolution of New cis-Regulatory Motifs Required for Cell-Specific Gene Expression in Caenorhabditis.

Michalis Barkoulas, Amhed M Vargas Velazquez, Alexandre E Peluffo, Marie-Anne Félix

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  6. Evolutionary Change in Gut Specification inJournal of developmental biology · 2023
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  8. Targeted DamID inScience advances · 2022
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  12. Review
  13. Physiological Starvation PromotesG3 (Bethesda, Md.) · 2018
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  14. Review
  15. The rewiring of transcription circuits in evolution.Current opinion in genetics & development · 2017
    Review
  16. Enhancer evolution and the origins of morphological novelty.Current opinion in genetics & development · 2017
    Review
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

4 authors at 1 institution in 2 countries.

Michalis BarkoulasInstitute of Biology of the Ecole Normale Supérieure (IBENS), CNRS, Inserm, Paris, France.ORCID 0000-0003-1974-7668
Amhed M Vargas VelazquezInstitute of Biology of the Ecole Normale Supérieure (IBENS), CNRS, Inserm, Paris, France.
Alexandre E PeluffoInstitute of Biology of the Ecole Normale Supérieure (IBENS), CNRS, Inserm, Paris, France.ORCID 0000-0001-7216-4205
Marie-Anne FélixInstitute of Biology of the Ecole Normale Supérieure (IBENS), CNRS, Inserm, Paris, France.
Centre National de la Recherche Scientifique · FR

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

Patterning of C. elegans vulval cell fates relies on inductive signaling. In this induction event, a single cell, the gonadal anchor cell, secretes LIN-3/EGF and induces three out of six competent precursor cells to acquire a vulval fate. We previously showed that this developmental system is robust to a four-fold variation in lin-3/EGF genetic dose. Here using single-molecule FISH, we find that the mean level of expression of lin-3 in the anchor cell is remarkably conserved. No change in lin-3 expression level could be detected among C. elegans wild isolates and only a low level of change-less than 30%-in the Caenorhabditis genus and in Oscheius tipulae. In C. elegans, lin-3 expression in the anchor cell is known to require three transcription factor binding sites, specifically two E-boxes and a nuclear-hormone-receptor (NHR) binding site. Mutation of any of these three elements in C. elegans results in a dramatic decrease in lin-3 expression. Yet only a single E-box is found in the Drosophilae supergroup of Caenorhabditis species, including C. angaria, while the NHR-binding site likely only evolved at the base of the Elegans group. We find that a transgene from C. angaria bearing a single E-box is sufficient for normal expression in C. elegans. Even a short 58 bp cis-regulatory fragment from C. angaria with this single E-box is able to replace the three transcription factor binding sites at the endogenous C. elegans lin-3 locus, resulting in the wild-type expression level. Thus, regulatory evolution occurring in cis within a 58 bp lin-3 fragment, results in a strict requirement for the NHR binding site and a second E-box in C. elegans. This single-cell, single-molecule, quantitative and functional evo-devo study demonstrates that conserved expression levels can hide extensive change in cis-regulatory site requirements and highlights the evolution of new cis-regulatory elements required for cell-specific gene expression.

Indexed as

AnimalsBody PatterningCaenorhabditis elegansCaenorhabditis elegans ProteinsCell DifferentiationDrosophilaE-Box ElementsEpidermal Growth FactorFemaleGene Expression Regulation, DevelopmentalProtein BindingReceptors, Cytoplasmic and NuclearRegulatory Sequences, Nucleic AcidSingle-Cell AnalysisVulvaCaenorhabditis elegans ProteinsEpidermal Growth FactorLin-3 protein, C elegansReceptors, Cytoplasmic and Nuclear

Identifiers

PMID27588814
PMCPMC5010242
OpenAlexW2510364534

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.