Evidence map›Paper›PMID 23468638›Full record

ArticlePLoS genetics2013

Rearrangements of 2.5 kilobases of noncoding DNA from the Drosophila even-skipped locus define predictive rules of genomic cis-regulatory logic.

Ah-Ram Kim, Carlos Martinez, John Ionides, Alexandre F Ramos, Michael Z Ludwig, Nobuo Ogawa, David H Sharp, John Reinitz

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 72 citations in OpenAlex.

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  7. A synthetic synthesis to explore animal evolution and development.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
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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

8 authors at 6 institutions in 3 countries.

Ah-Ram KimDepartment of Ecology and Evolution, Chicago Center for Systems Biology, University of Chicago, Chicago, Illinois, USA.
Carlos Martinez
John Ionides
Alexandre F Ramos
Michael Z Ludwig
Nobuo Ogawa
David H Sharp
John Reinitz
Center for Systems Biology · USLawrence Berkeley National Laboratory · USLos Alamos National Laboratory · USUniversidade de São Paulo · BRUniversity of Cambridge · GBUniversity of Chicago · US

Funding

CORE: ADMINISTRATIVEP50GM081892 · NIGMS · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2008 to 2013
$15.9M
Transcription Network Controlling Drosophila DevelopmentR01GM070444 · NIGMS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI BIGGIN, MARK D · 2003 to 2007
$14.9M
PHYSIOLOGICAL MODEL OF GENE REGULATION IN DROSOPHILAR01RR007801 · NCRR · UNIVERSITY OF CHICAGO · PI REINITZ, JOHN B. · 1992 to 2011
$6.3M
Physiological Model of Gene Regulation in DrosophilaR01OD010936 · OD · UNIVERSITY OF CHICAGO · PI ALLESINA, STEFANO, LUDWIG, MICHAEL · 2012 to 2023
$6.3M
NCRR NIH HHS R01 RR007801NIGMS NIH HHS P50 GM081892NIGMS NIH HHS R01 GM070444NIGMS NIH HHS R01 GM70444NIH HHS R01 OD010936
6 · The paper itself

Abstract

Rearrangements of about 2.5 kilobases of regulatory DNA located 5' of the transcription start site of the Drosophila even-skipped locus generate large-scale changes in the expression of even-skipped stripes 2, 3, and 7. The most radical effects are generated by juxtaposing the minimal stripe enhancers MSE2 and MSE3 for stripes 2 and 3 with and without small "spacer" segments less than 360 bp in length. We placed these fusion constructs in a targeted transformation site and obtained quantitative expression data for these transformants together with their controlling transcription factors at cellular resolution. These data demonstrated that the rearrangements can alter expression levels in stripe 2 and the 2-3 interstripe by a factor of more than 10. We reasoned that this behavior would place tight constraints on possible rules of genomic cis-regulatory logic. To find these constraints, we confronted our new expression data together with previously obtained data on other constructs with a computational model. The model contained representations of thermodynamic protein-DNA interactions including steric interference and cooperative binding, short-range repression, direct repression, activation, and coactivation. The model was highly constrained by the training data, which it described within the limits of experimental error. The model, so constrained, was able to correctly predict expression patterns driven by enhancers for other Drosophila genes; even-skipped enhancers not included in the training set; stripe 2, 3, and 7 enhancers from various Drosophilid and Sepsid species; and long segments of even-skipped regulatory DNA that contain multiple enhancers. The model further demonstrated that elevated expression driven by a fusion of MSE2 and MSE3 was a consequence of the recruitment of a portion of MSE3 to become a functional component of MSE2, demonstrating that cis-regulatory "elements" are not elementary objects.

Indexed as

Drosophila melanogasterEnhancer Elements, GeneticAnimalsBinding SitesDNA-Binding ProteinsDrosophila ProteinsEvolution, MolecularGene Expression Regulation, DevelopmentalGene RearrangementGenomeHomeodomain ProteinsRNA, UntranslatedTranscription FactorsTranscription Initiation SiteDNA-Binding ProteinsDrosophila Proteinseve protein, DrosophilaHomeodomain ProteinsRNA, UntranslatedTranscription Factors

Identifiers

PMID23468638
PMCPMC3585115
OpenAlexW2056707311

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.