Evidence map›Paper›PMID 27070787›Full record

ArticlePLoS genetics2016

Control of Neural Daughter Cell Proliferation by Multi-level Notch/Su(H)/E(spl)-HLH Signaling.

Caroline Bivik, Ryan B MacDonald, Erika Gunnar, Khalil Mazouni, Francois Schweisguth, Stefan Thor

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Preclinical mouse models for studying cholangiocarcinoma.Liver research (Beijing, China) · 2026
    Review
  2. Indirect neurogenesis in space and time.Nature reviews. Neuroscience · 2024
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Notch Signalling in Breast Development and Cancer.Frontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Temporal patterning in neural progenitors: fromDisease models & mechanisms · 2020
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

6 authors.

Caroline BivikDepartment of Clinical and Experimental Medicine, Linkoping University, Linkoping, Sweden.
Ryan B MacDonaldDepartment of Clinical and Experimental Medicine, Linkoping University, Linkoping, Sweden.
Erika GunnarDepartment of Clinical and Experimental Medicine, Linkoping University, Linkoping, Sweden.
Khalil MazouniInstitut Pasteur, Paris, France.
Francois SchweisguthInstitut Pasteur, Paris, France.
Stefan ThorDepartment of Clinical and Experimental Medicine, Linkoping University, Linkoping, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch pathway controls proliferation during development and in adulthood, and is frequently affected in many disorders. However, the genetic sensitivity and multi-layered transcriptional properties of the Notch pathway has made its molecular decoding challenging. Here, we address the complexity of Notch signaling with respect to proliferation, using the developing Drosophila CNS as model. We find that a Notch/Su(H)/E(spl)-HLH cascade specifically controls daughter, but not progenitor proliferation. Additionally, we find that different E(spl)-HLH genes are required in different neuroblast lineages. The Notch/Su(H)/E(spl)-HLH cascade alters daughter proliferation by regulating four key cell cycle factors: Cyclin E, String/Cdc25, E2f and Dacapo (mammalian p21CIP1/p27KIP1/p57Kip2). ChIP and DamID analysis of Su(H) and E(spl)-HLH indicates direct transcriptional regulation of the cell cycle genes, and of the Notch pathway itself. These results point to a multi-level signaling model and may help shed light on the dichotomous proliferative role of Notch signaling in many other systems.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsBinding SitesCell CommunicationCell Cycle ProteinsCell LineageCell ProliferationCentral Nervous SystemCyclin EDrosophilaDrosophila ProteinsE2F Transcription FactorsEmbryo, NonmammalianGene Expression Regulation, DevelopmentalNuclear ProteinsProtein Tyrosine PhosphatasesBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsCyclin Edap protein, DrosophilaDrosophila ProteinsE2f1 protein, DrosophilaE2F Transcription FactorsE(spl)m7-HLH protein, DrosophilaN protein, DrosophilaNuclear ProteinsProtein Tyrosine PhosphatasesReceptors, NotchRepressor Proteinsstg protein, DrosophilaSu(H) protein, DrosophilaTranscription Factors

Identifiers

PMID27070787
PMCPMC4829154

What OpenQuestion holds

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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.