Evidence map›Paper›PMID 8665855›Full record

ArticleThe EMBO journal1996

An extradenticle-induced conformational change in a HOX protein overcomes an inhibitory function of the conserved hexapeptide motif.

S K Chan, H Pöpperl, R Krumlauf, R S Mann

Open access · greenAbstract readComparative Study
In one paragraph

Article in The EMBO journal, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Anterior Hox Genes and the Process of Cephalization.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Article
  9. Hindbrain induction and patterning during early vertebrate development.Cellular and molecular life sciences : CMLS · 2019
    Review
  10. Mechanisms of Specificity for Hox Factor Activity.Journal of developmental biology · 2016
    Article
  11. Article
  12. Article
  13. Redox signaling in cardiac renewal.Antioxidants & redox signaling · 2014
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Pbx homeodomain proteins: TALEnted regulators of limb patterning and outgrowth.Developmental dynamics : an official publication of the American Association of Anatomists · 2011
    Review
  19. Selection of distinct Hox-Extradenticle interaction modes fine-tunes Hox protein activity.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  20. 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

4 authors at 1 institution in 1 country.

S K ChanDepartment of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
H Pöpperl
R Krumlauf
R S Mann
Columbia University · US

Funding

MOLECULAR GENETICS OF SEGMENT IDENTITYR01GM054510 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MANN, RICHARD S · 1996 to 2015
$5.5M
NIGMS NIH HHS R01 GM054510
6 · The paper itself

Abstract

HOX homeoproteins control cell identities during animal development by differentially regulating target genes. The homeoprotein encoded by the extradenticle (exd) gene can selectively modify HOX DNA binding, suggesting that it contributes to HOX specificity in vivo. HOX-EXD interactions are in part mediated by a conserved stretch of amino acids termed the hexapeptide found in many HOX proteins. Here, we demonstrate that a 20 bp oligonucleotide from the 5' region of the mouse Hoxb-1 gene, a homolog of Drosophila labial (lab), is sufficient to direct an expression pattern in Drosophila that is very similar to endogenous lab. In vivo, this expression requires lab and exd and, in vitro, LAB requires EXD to bind this oligonucleotide. In contrast, LAB proteins with mutations in the hexapeptide bind DNA even in the absence of EXD. Moreover, a hexapeptide mutant of LAB has an increased ability to activate transcription in vivo. Partial proteolysis experiments suggest that EXD can induce a conformational change in LAB. These data are consistent with a mechanism whereby the LAB hexapeptide inhibits LAB function by inhibiting DNA binding and that an EXD-induced conformational change in LAB relieves this inhibition, promoting highly specific interactions with biologically relevant binding sites.

Indexed as

Drosophila ProteinsGene Expression Regulation, DevelopmentalProtein ConformationAmino Acid SequenceAnimalsBinding SitesDNADNA-Binding ProteinsDrosophila melanogasterEnhancer Elements, GeneticHomeodomain ProteinsInsect HormonesMiceMolecular Sequence DataProtein BindingProtein Structure, TertiaryDNADNA-Binding ProteinsDrosophila Proteinsexd protein, DrosophilaHomeodomain ProteinsInsect Hormoneslab protein, DrosophilaRecombinant Fusion ProteinsTranscription Factors

Identifiers

PMID8665855
PMCPMC450180
OpenAlexW214611139

What OpenQuestion holds

Textmetadata
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.