Evidence map›Paper›PMID 30028887›Full record

ArticlePLoS genetics2018

Lateral inhibition: Two modes of non-autonomous negative autoregulation by neuralized.

Steven W Miller, James W Posakony

Abstract read
In one paragraph

Article in PLoS genetics, 2018. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Cis-inhibition suppresses basal Notch signaling during sensory organ precursor selection.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Article
  7. 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

2 authors.

Steven W MillerDivision of Biological Sciences, Section of Cell & Developmental Biology, University of California San Diego, La Jolla, California, United States of America.ORCID 0000-0001-7610-6336
James W PosakonyDivision of Biological Sciences, Section of Cell & Developmental Biology, University of California San Diego, La Jolla, California, United States of America.ORCID 0000-0001-6377-1732

Funding

MOLECULAR GENETICS OF SENSORY ORGAN DEVELOPMENTR01GM046993 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI POSAKONY, JAMES W. · 1992 to 2015
$3.5M
Functional Architecture of Developmental Cis-Regulatory ModulesR01GM120377 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI POSAKONY, JAMES W. · 2017 to 2020
$1.2M
NIGMS NIH HHS R01 GM046993NIGMS NIH HHS R01 GM120377
6 · The paper itself

Abstract

Developmental patterning involves the progressive subdivision of tissue into different cell types by invoking different genetic programs. In particular, cell-cell signaling is a universally deployed means of specifying distinct cell fates in adjacent cells. For this mechanism to be effective, it is essential that an asymmetry be established in the signaling and responding capacities of the participating cells. Here we focus on the regulatory mechanisms underlying the role of the neuralized gene and its protein product in establishing and maintaining asymmetry of signaling through the Notch pathway. The context is the classical process of "lateral inhibition" within Drosophila proneural clusters, which is responsible for distinguishing the sensory organ precursor (SOP) and non-SOP fates among adjacent cells. We find that neur is directly regulated in proneural clusters by both proneural transcriptional activators and Enhancer of split basic helix-loop-helix repressors (bHLH-Rs), via two separate cis-regulatory modules within the neur locus. We show that this bHLH-R regulation is required to prevent the early, pre-SOP expression of neur from being maintained in a subset of non-SOPs following SOP specification. Lastly, we demonstrate that Neur activity in the SOP is required to inhibit, in a cell non-autonomous manner, both neur expression and Neur function in non-SOPs, thus helping to secure the robust establishment of distinct cell identities within the developing proneural cluster.

Indexed as

AnimalsAnimals, Genetically ModifiedBasic Helix-Loop-Helix ProteinsCell CommunicationDrosophila melanogasterDrosophila ProteinsFemaleGene Expression Regulation, DevelopmentalHomeostasisMaleReceptors, NotchRegulatory Elements, TranscriptionalRepressor ProteinsSignal TransductionUbiquitin-Protein LigasesBasic Helix-Loop-Helix ProteinsDrosophila ProteinsE(spl)m7-HLH protein, Drosophilaneur protein, DrosophilaReceptors, NotchRepressor ProteinsUbiquitin-Protein Ligases

Identifiers

PMID30028887
PMCPMC6070291

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.