Evidence map›Paper›PMID 21283833›Full record

ArticlePLoS biology2011

The gene regulatory cascade linking proneural specification with differentiation in Drosophila sensory neurons.

Sebastián Cachero, T Ian Simpson, Petra I Zur Lage, Lina Ma, Fay G Newton, Eimear E Holohan, J Douglas Armstrong, Andrew P Jarman

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 59 citations in OpenAlex.

  1. Foxn3 is required to suppress aberrant ciliogenesis in nonphotoreceptor retinal neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Cilia and transcription: a mini review.Frontiers in cell and developmental biology · 2025
    Review
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  6. AFrontiers in cell and developmental biology · 2022
    Article
  7. Article
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  9. Survey of the Ciliary Motility Machinery ofFrontiers in genetics · 2019
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Gastric pouches and the mucociliary sole: setting the stage for nervous system evolution.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  18. Article
  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

8 authors at 1 institution in 1 country.

Sebastián CacheroCentre for Integrative Physiology, School of Biomedical Sciences, University of Edinburgh, Edinburgh, United Kingdom.
T Ian Simpson
Petra I Zur Lage
Lina Ma
Fay G Newton
Eimear E Holohan
J Douglas Armstrong
Andrew P Jarman
University of Edinburgh · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I004491/1Wellcome Trust 077266
6 · The paper itself

Abstract

In neurogenesis, neural cell fate specification is generally triggered by proneural transcription factors. Whilst the role of proneural factors in fate specification is well studied, the link between neural specification and the cellular pathways that ultimately must be activated to construct specialised neurons is usually obscure. High-resolution temporal profiling of gene expression reveals the events downstream of atonal proneural gene function during the development of Drosophila chordotonal (mechanosensory) neurons. Among other findings, this reveals the onset of expression of genes required for construction of the ciliary dendrite, a key specialisation of mechanosensory neurons. We determine that atonal activates this cellular differentiation pathway in several ways. Firstly, atonal directly regulates Rfx, a well-known highly conserved ciliogenesis transcriptional regulator. Unexpectedly, differences in Rfx regulation by proneural factors may underlie variations in ciliary dendrite specialisation in different sensory neuronal lineages. In contrast, fd3F encodes a novel forkhead family transcription factor that is exclusively expressed in differentiating chordotonal neurons. fd3F regulates genes required for specialized aspects of chordotonal dendrite physiology. In addition to these intermediate transcriptional regulators, we show that atonal directly regulates a novel gene, dilatory, that is directly associated with ciliogenesis during neuronal differentiation. Our analysis demonstrates how early cell fate specification factors can regulate structural and physiological differentiation of neuronal cell types. It also suggests a model for how subtype differentiation in different neuronal lineages may be regulated by different proneural factors. In addition, it provides a paradigm for how transcriptional regulation may modulate the ciliogenesis pathway to give rise to structurally and functionally specialised ciliary dendrites.

Indexed as

Gene Expression ProfilingUp-RegulationAnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell LineCiliaDNA-Binding ProteinsDrosophilaDrosophila ProteinsForkhead Transcription FactorsGenes, ReporterLarvaNerve Tissue ProteinsRegulatory Factor X Transcription FactorsSensory Receptor Cellsato protein, DrosophilaBasic Helix-Loop-Helix Proteinsdila protein, DrosophilaDNA-Binding ProteinsDrosophila Proteinsfd3F protein, DrosophilaForkhead Transcription FactorsNerve Tissue ProteinsRegulatory Factor X Transcription Factorssc protein, DrosophilaTranscription Factors

Identifiers

PMID21283833
PMCPMC3023811
OpenAlexW1984500085

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.