Evidence map›Paper›PMID 31199038›Full record

ArticleMolecular reproduction and development2019

Single cell RNA-seq in the sea urchin embryo show marked cell-type specificity in the Delta/Notch pathway.

Stephany Foster, Yee Voan Teo, Nicola Neretti, Nathalie Oulhen, Gary M Wessel

Open access · greenAbstract read
In one paragraph

Article in Molecular reproduction and development, 2019. 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
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Stephany FosterDepartment of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Yee Voan TeoDepartment of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Nicola NerettiDepartment of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Nathalie OulhenDepartment of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Gary M WesselDepartment of Molecular and Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.ORCID 0000-0002-1210-9279
Brown University · US

Funding

The role of Sirtuins in neurodegenerative diseaseP20GM109035 · NIGMS · BROWN UNIVERSITY · PI LIU, YAJUN · 2016 to 2025
$22.6M
Stem Cells and AgingP20GM119943 · NIGMS · RHODE ISLAND HOSPITAL · PI QUESENBERRY, PETER J. · 2017 to 2021
$10.6M
The Role of Somatic Transposition in Age-associated Genomic InstabilityR01AG050582 · NIA · BROWN UNIVERSITY · PI NERETTI, NICOLA, SEDIVY, JOHN M · 2017 to 2022
$2.2M
Mechanisms of quiescence in primordial germ cellsR01GM125071 · NIGMS · BROWN UNIVERSITY · PI WESSEL, GARY M · 2017 to 2020
$1.4M
NIA NIH HHS R01 AG050582NIGMS NIH HHS P20 GM109035NIGMS NIH HHS P20 GM119943NIGMS NIH HHS R01 GM125071
6 · The paper itself

Abstract

Sea urchin embryos are excellent for in vivo functional studies because of their transparency and tractability in manipulation. They are also favorites for pharmacological approaches since they develop in an aquatic environment and addition of test substances is straightforward. A concern in many pharmacological tests though is the potential for pleiotropic effects that confound the conclusions drawn from the results. Precise cellular interpretations are often not feasible because the impact of the perturbant is not known. Here we use single-cell mRNA (messenger RNA) sequencing as a metric of cell types in the embryo and to determine the selectivity of two commonly used inhibitors, one each for the Wnt and the Delta-Notch pathways, on these nascent cell types. We identified 11 distinct cell types based on mRNA profiling, and that the cell lineages affected by Wnt and Delta/Notch inhibition were distinct from each other. These data support specificity and distinct effects of these signaling pathways in the embryo and illuminate how these conserved pathways selectively regulate cell lineages at a single cell level. Overall, we conclude that single cell RNA-seq analysis in this embryo is revealing of the cell types present during development, of the changes in the gene regulatory network resulting from inhibition of various signaling pathways, and of the selectivity of these pathways in influencing developmental trajectories.

Indexed as

Gene Expression Regulation, DevelopmentalIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchRNA-SeqSignal TransductionSingle-Cell AnalysisAnimalsEmbryo, NonmammalianSea Urchinsdelta proteinIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchDelta/Notch pathwaydrop-seqsea urchin embryosingle-cell RNA-seqWnt pathway

Identifiers

PMID31199038
PMCPMC6690749
OpenAlexW2951198768

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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.