Evidence map›Paper›PMID 28414802›Full record

ArticlePLoS genetics2017

Neuronal cell fate specification by the molecular convergence of different spatio-temporal cues on a common initiator terminal selector gene.

Johannes Stratmann, Stefan Thor

Abstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. A brain-specific microRNA,Genes & development · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
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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.

Johannes StratmannDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Stefan ThorDepartment of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.ORCID 0000-0001-5095-541X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extensive genetic regulatory flows underlying specification of different neuronal subtypes are not well understood at the molecular level. The Nplp1 neuropeptide neurons in the developing Drosophila nerve cord belong to two sub-classes; Tv1 and dAp neurons, generated by two distinct progenitors. Nplp1 neurons are specified by spatial cues; the Hox homeotic network and GATA factor grn, and temporal cues; the hb -> Kr -> Pdm -> cas -> grh temporal cascade. These spatio-temporal cues combine into two distinct codes; one for Tv1 and one for dAp neurons that activate a common terminal selector feedforward cascade of col -> ap/eya -> dimm -> Nplp1. Here, we molecularly decode the specification of Nplp1 neurons, and find that the cis-regulatory organization of col functions as an integratory node for the different spatio-temporal combinatorial codes. These findings may provide a logical framework for addressing spatio-temporal control of neuronal sub-type specification in other systems.

Indexed as

NeuronsAnimalsBasic Helix-Loop-Helix ProteinsBody PatterningCell DifferentiationCell LineageDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEye ProteinsGATA Transcription FactorsGene Expression Regulation, DevelopmentalGene Regulatory NetworksHomeodomain ProteinsLIM-Homeodomain ProteinsNeuropeptidesap protein, DrosophilaBasic Helix-Loop-Helix Proteinscas protein, Drosophiladimm protein, DrosophilaDNA-Binding ProteinsDrosophila Proteinseya protein, DrosophilaEye ProteinsGATA Transcription Factorsgrn protein, DrosophilaHomeodomain ProteinsLIM-Homeodomain ProteinsNeuropeptidesNplp1 protein, Drosophilanub protein, DrosophilaPOU Domain FactorsTranscription Factors

Identifiers

PMID28414802
PMCPMC5411104

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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.