Evidence map›Paper›PMID 31159833›Full record

ArticleGenome biology2019

Chromatin accessibility plays a key role in selective targeting of Hox proteins.

Damiano Porcelli, Bettina Fischer, Steven Russell, Robert White

Abstract read
In one paragraph

Article in Genome biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Chromatin enables precise and scalable gene regulation with factors of limited specificity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Floral Homeotic Factors: A Question of Specificity.Plants (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Article
  11. Micromanagement ofJournal of developmental biology · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Mechanisms Underlying Hox-Mediated Transcriptional Outcomes.Frontiers in cell and developmental biology · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. 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.

Damiano PorcelliDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, CB2 3DY, UK.
Bettina FischerDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Steven RussellDepartment of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK.
Robert WhiteDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, CB2 3DY, UK. rw108@cam.ac.uk.ORCID 0000-0002-0019-8227

Funding

Biotechnology and Biological Sciences Research Council BB/M007081/1
6 · The paper itself

Abstract

backgroundHox transcription factors specify segmental diversity along the anterior-posterior body axis in metazoans. While the different Hox family members show clear functional specificity in vivo, they all show similar binding specificity in vitro and a satisfactory understanding of in vivo Hox target selectivity is still lacking.

resultsUsing transient transfection in Kc167 cells, we systematically analyze the binding of all eight Drosophila Hox proteins. We find that Hox proteins show considerable binding selectivity in vivo even in the absence of canonical Hox cofactors Extradenticle and Homothorax. Hox binding selectivity is strongly associated with chromatin accessibility, being highest in less accessible chromatin. Individual Hox proteins exhibit different propensities to bind less accessible chromatin, and high binding selectivity is associated with high-affinity binding regions, leading to a model where Hox proteins derive binding selectivity through affinity-based competition with nucleosomes. Extradenticle/Homothorax cofactors generally facilitate Hox binding, promoting binding to regions in less accessible chromatin but with little effect on the overall selectivity of Hox targeting. These cofactors collaborate with Hox proteins in opening chromatin, in contrast to the pioneer factor, Glial cells missing, which facilitates Hox binding by independently generating accessible chromatin regions.

conclusionsThese studies indicate that chromatin accessibility plays a key role in Hox selectivity. We propose that relative chromatin accessibility provides a basis for subtle differences in binding specificity and affinity to generate significantly different sets of in vivo genomic targets for different Hox proteins.

Indexed as

Chromatin Assembly and DisassemblyAmino Acid MotifsAnimalsCell LineChromatinDrosophilaDrosophila ProteinsHomeodomain ProteinsTranscription FactorsChromatinDrosophila Proteinsexd protein, DrosophilaHomeodomain Proteinshth protein, DrosophilaTranscription FactorsChromatinChromatin accessibilityHox cofactorsHox geneHox proteinTranscription factorTranscription factor selectivity

Identifiers

PMID31159833
PMCPMC6547607

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.