Evidence map›Paper›PMID 18803772›Full record

ArticleEvolution & development

Evolution of an insect-specific GROUCHO-interaction motif in the ENGRAILED selector protein.

Chris Todd Hittinger, Sean B Carroll

Abstract read
In one paragraph

Article in Evolution & development. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Short linear motifs - ex nihilo evolution of protein regulation.Cell communication and signaling : CCS · 2015
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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

2 authors at 1 institution in 1 country.

Chris Todd HittingerLaboratory of Genetics, Howard Hughes Medical Institute, University of Wisconsin-Madison, Madison, WI 53706-1534, USA.
Sean B Carroll
University of Wisconsin–Madison · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOMIC SCIENCET32HG000045 · NHGRI · WASHINGTON UNIVERSITY · PI MICHAEL R BRENT, Barak A Cohen · 1997 to 2026
$8.4M
Howard Hughes Medical InstituteNHGRI NIH HHS 5T32HG00045NHGRI NIH HHS T32 HG000045
6 · The paper itself

Abstract

Animal morphology evolves through alterations in the genetic regulatory networks that control development. Regulatory connections are commonly added, subtracted, or modified via mutations in cis-regulatory elements, but several cases are also known where transcription factors have gained or lost activity-modulating peptide motifs. In order to better assess the role of novel transcription factor peptide motifs in evolution, we searched for synapomorphic motifs in the homeotic selectors of Drosophila melanogaster and related insects. Here, we describe an evolutionarily novel GROUCHO (GRO)-interaction motif in the ENGRAILED (EN) selector protein. This "ehIFRPF" motif is not homologous to the previously characterized "engrailed homology 1" (eh1) GRO-interaction motif of EN. This second motif is an insect-specific "WRPW"-type motif that has been maintained by purifying selection in at least the dipteran/lepidopteran lineage. We demonstrate that this motif contributes to in vivo repression of the wingless (wg) target gene and to interaction with GRO in vitro. The acquisition and conservation of this auxiliary peptide motif shows how the number and activity of short peptide motifs can evolve in transcription factors while existing regulatory functions are maintained.

Indexed as

Evolution, MolecularAnimalsBase SequenceBasic Helix-Loop-Helix ProteinsDNA PrimersDrosophila ProteinsHomeodomain ProteinsImmunohistochemistryInsectaRepressor ProteinsTranscription FactorsBasic Helix-Loop-Helix ProteinsDNA PrimersDrosophila ProteinsEn protein, Drosophilagro protein, DrosophilaHomeodomain ProteinsRepressor ProteinsTranscription Factors

Identifiers

PMID18803772
PMCPMC2597661
OpenAlexW2008592915

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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.