Evidence map›Paper›PMID 24945987›Full record

ArticlePLoS computational biology2014

An expanded Notch-Delta model exhibiting long-range patterning and incorporating MicroRNA regulation.

Jerry S Chen, Abygail M Gumbayan, Robert W Zeller, Joseph M Mahaffy

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Role of domain in pattern formation.Development, growth & differentiation · 2017
    Review
  7. Jagged-Delta asymmetry in Notch signaling can give rise to a Sender/Receiver hybrid phenotype.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  8. 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

4 authors at 1 institution in 1 country.

Jerry S ChenComputational Science Research Center, San Diego State University, San Diego, California, United States of America; Department of Biology, San Diego State University, San Diego, California, United States of America.
Abygail M GumbayanDepartment of Biology, San Diego State University, San Diego, California, United States of America.
Robert W ZellerComputational Science Research Center, San Diego State University, San Diego, California, United States of America; Department of Biology, San Diego State University, San Diego, California, United States of America.
Joseph M MahaffyComputational Science Research Center, San Diego State University, San Diego, California, United States of America; Department of Mathematics and Statistics, San Diego State University, San Diego, California, United States of America.
San Diego State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Notch-Delta signaling is a fundamental cell-cell communication mechanism that governs the differentiation of many cell types. Most existing mathematical models of Notch-Delta signaling are based on a feedback loop between Notch and Delta leading to lateral inhibition of neighboring cells. These models result in a checkerboard spatial pattern whereby adjacent cells express opposing levels of Notch and Delta, leading to alternate cell fates. However, a growing body of biological evidence suggests that Notch-Delta signaling produces other patterns that are not checkerboard, and therefore a new model is needed. Here, we present an expanded Notch-Delta model that builds upon previous models, adding a local Notch activity gradient, which affects long-range patterning, and the activity of a regulatory microRNA. This model is motivated by our experiments in the ascidian Ciona intestinalis showing that the peripheral sensory neurons, whose specification is in part regulated by the coordinate activity of Notch-Delta signaling and the microRNA miR-124, exhibit a sparse spatial pattern whereby consecutive neurons may be spaced over a dozen cells apart. We perform rigorous stability and bifurcation analyses, and demonstrate that our model is able to accurately explain and reproduce the neuronal pattern in Ciona. Using Monte Carlo simulations of our model along with miR-124 transgene over-expression assays, we demonstrate that the activity of miR-124 can be incorporated into the Notch decay rate parameter of our model. Finally, we motivate the general applicability of our model to Notch-Delta signaling in other animals by providing evidence that microRNAs regulate Notch-Delta signaling in analogous cell types in other organisms, and by discussing evidence in other organisms of sparse spatial patterns in tissues where Notch-Delta signaling is active.

Indexed as

Models, NeurologicalAnimalsAnimals, Genetically ModifiedBody PatterningCell CommunicationCiona intestinalisComputational BiologyComputer SimulationGene Expression Regulation, DevelopmentalIntracellular Signaling Peptides and ProteinsMembrane ProteinsMicroRNAsMonte Carlo MethodNervous SystemReceptors, NotchSensory Receptor Cellsdelta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsMicroRNAsMIRN124 microRNA, C elegansReceptors, Notch

Identifiers

PMID24945987
PMCPMC4063677
OpenAlexW2009727747

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.