Evidence map›Paper›PMID 28974640›Full record

ArticleDevelopment (Cambridge, England)2017

Differential interactions between Notch and ID factors control neurogenesis by modulating Hes factor autoregulation.

Marcelo Boareto, Dagmar Iber, Verdon Taylor

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

3 authors at 2 institutions in 1 country.

Marcelo BoaretoDepartment of Biosystems Science and Engineering (D-BSSE), ETH Zurich, Mattenstrasse 26, 4058 Basel, Switzerland marcelo.boareto@bsse.ethz.ch dagmar.iber@bsse.ethz.ch verdon.taylor@unibas.ch.
Dagmar IberDepartment of Biosystems Science and Engineering (D-BSSE), ETH Zurich, Mattenstrasse 26, 4058 Basel, Switzerland marcelo.boareto@bsse.ethz.ch dagmar.iber@bsse.ethz.ch verdon.taylor@unibas.ch.
Verdon TaylorDepartment of Biomedicine, University of Basel, Mattenstrasse 28, 4058 Basel, Switzerland marcelo.boareto@bsse.ethz.ch dagmar.iber@bsse.ethz.ch verdon.taylor@unibas.ch.ORCID 0000-0003-3497-5976
SIB Swiss Institute of Bioinformatics · CHUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During embryonic and adult neurogenesis, neural stem cells (NSCs) generate the correct number and types of neurons in a temporospatial fashion. Control of NSC activity and fate is crucial for brain formation and homeostasis. Neurogenesis in the embryonic and adult brain differ considerably, but Notch signaling and inhibitor of DNA-binding (ID) factors are pivotal in both. Notch and ID factors regulate NSC maintenance; however, it has been difficult to evaluate how these pathways potentially interact. Here, we combined mathematical modeling with analysis of single-cell transcriptomic data to elucidate unforeseen interactions between the Notch and ID factor pathways. During brain development, Notch signaling dominates and directly regulates Id4 expression, preventing other ID factors from inducing NSC quiescence. Conversely, during adult neurogenesis, Notch signaling and Id2/3 regulate neurogenesis in a complementary manner and ID factors can induce NSC maintenance and quiescence in the absence of Notch. Our analyses unveil key molecular interactions underlying NSC maintenance and mechanistic differences between embryonic and adult neurogenesis. Similar Notch and ID factor interactions may be crucial in other stem cell systems.

Indexed as

HomeostasisNeurogenesisAnimalsCell DifferentiationCell ProliferationComputer SimulationEmbryo, MammalianFeedback, PhysiologicalGene Expression Regulation, DevelopmentalHumansMiceModels, BiologicalNeural Stem CellsProtein BindingReceptors, NotchSignal TransductionHES1 protein, humanHes1 protein, mouseReceptors, NotchTranscription Factor HES-1Computational biologyId transcription factorsNeural stem cellsNeurogenesisNotch signaling

Identifiers

PMID28974640
PMCPMC5665482
OpenAlexW2764337959

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.