Evidence map›Paper›PMID 21821017›Full record

ArticleDevelopmental biology2011

Molecular dissection of cis-regulatory modules at the Drosophila bithorax complex reveals critical transcription factor signature motifs.

Michael O Starr, Margaret C W Ho, Eric J M Gunther, Yen-Kuei Tu, Andrey S Shur, Sara E Goetz, Matthew J Borok, Victoria Kang, Robert A Drewell

Abstract read
In one paragraph

Article in Developmental biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

  1. Developmental patterning of adipose tissue bybioRxiv : the preprint server for biology · 2026
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  7. Boundary Bypass Activity in thebioRxiv : the preprint server for biology · 2023
    Article
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  11. Homeotic Genes: Clustering, Modularity, and Diversity.Frontiers in cell and developmental biology · 2021
    Review
  12. Article
  13. Article
  14. Sex combs reduced (Scr) regulatory region of Drosophila revisited.Molecular genetics and genomics : MGG · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

9 authors at 1 institution in 1 country.

Michael O StarrBiology Department, Harvey Mudd College, Claremont, CA 91711, USA.
Margaret C W Ho
Eric J M Gunther
Yen-Kuei Tu
Andrey S Shur
Sara E Goetz
Matthew J Borok
Victoria Kang
Robert A Drewell
Harvey Mudd College · US

Funding

Molecular Dissection of Drosophila Hox Gene Cis-Regulatory ModulesR15GM090167 · NIGMS · HARVEY MUDD COLLEGE · PI DREWELL, ROBERT A · 2010 to 2010
$204k
Promoter-Enhancer Interactions at the Drosophila Bithorax ComplexR03HD054977 · NICHD · HARVEY MUDD COLLEGE · PI DREWELL, ROBERT A · 2007 to 2008
$125k
Howard Hughes Medical InstituteNICHD NIH HHS HD54977NICHD NIH HHS R03 HD054977NIGMS NIH HHS GM090167NIGMS NIH HHS R15 GM090167
6 · The paper itself

Abstract

At the Drosophila melanogaster bithorax complex (BX-C) over 330kb of intergenic DNA is responsible for directing the transcription of just three homeotic (Hox) genes during embryonic development. A number of distinct enhancer cis-regulatory modules (CRMs) are responsible for controlling the specific expression patterns of the Hox genes in the BX-C. While it has proven possible to identify orthologs of known BX-C CRMs in different Drosophila species using overall sequence conservation, this approach has not proven sufficiently effective for identifying novel CRMs or defining the key functional sequences within enhancer CRMs. Here we demonstrate that the specific spatial clustering of transcription factor (TF) binding sites is important for BX-C enhancer activity. A bioinformatic search for combinations of putative TF binding sites in the BX-C suggests that simple clustering of binding sites is frequently not indicative of enhancer activity. However, through molecular dissection and evolutionary comparison across the Drosophila genus we discovered that specific TF binding site clustering patterns are an important feature of three known BX-C enhancers. Sub-regions of the defined IAB5 and IAB7b enhancers were both found to contain an evolutionarily conserved signature motif of clustered TF binding sites which is critical for the functional activity of the enhancers. Together, these results indicate that the spatial organization of specific activator and repressor binding sites within BX-C enhancers is of greater importance than overall sequence conservation and is indicative of enhancer functional activity.

Indexed as

AnimalsBase SequenceBinding SitesConserved SequenceDrosophilaDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianEnhancer Elements, GeneticEvolution, MolecularGene Expression Regulation, DevelopmentalHomeodomain ProteinsIn Situ HybridizationModels, GeneticMolecular Sequence DataMultigene Familyabd-A protein, DrosophilaAbd-B proteins, DrosophilaDrosophila ProteinsHomeodomain ProteinsNuclear ProteinsTranscription FactorsUbx protein, Drosophila

Identifiers

PMID21821017
PMCPMC3202680
OpenAlexW2006996555

What OpenQuestion holds

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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.