Evidence map›Paper›PMID 37955383›Full record

ArticleJournal of visualized experiments : JoVE2023

Optogenetic Signaling Activation in Zebrafish Embryos.

Allison J Saul, Catherine E Rogers, Marcial Garmendia-Cedillos, Thomas Pohida, Katherine W Rogers

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

5 citing papers in PubMed, 2 citations in OpenAlex.

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  5. 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

5 authors at 2 institutions in 1 country.

Allison J Saul *Division of Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH.
Catherine E Rogers *Division of Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH.
Marcial Garmendia-CedillosInstrumentation Development and Engineering Application Solutions, National Institute of Biomedical Imaging and Bioengineering, NIH.
Thomas PohidaInstrumentation Development and Engineering Application Solutions, National Institute of Biomedical Imaging and Bioengineering, NIH.
Katherine W RogersDivision of Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH; katherine.rogers@nih.gov.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Institute of Biomedical Imaging and Bioengineering · US

Funding

Decoding developmental signaling during zebrafish embryogenesisZIAHD009002 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI ROGERS, KATHERINE · 2022 to 2025
$5.1M
Intramural NIH HHS ZIA HD009002
6 · The paper itself

Abstract

Signaling pathways orchestrate fundamental biological processes, including development, regeneration, homeostasis, and disease. Methods to experimentally manipulate signaling are required to understand how signaling is interpreted in these wide-ranging contexts. Molecular optogenetic tools can provide reversible, tunable manipulations of signaling pathway activity with a high degree of spatiotemporal control and have been applied in vitro, ex vivo, and in vivo. These tools couple light-responsive protein domains, such as the blue light homodimerizing light-oxygen-voltage sensing (LOV) domain, with signaling effectors to confer light-dependent experimental control over signaling. This protocol provides practical guidelines for using the LOV-based bone morphogenetic protein (BMP) and Nodal signaling activators bOpto-BMP and bOpto-Nodal in the optically accessible early zebrafish embryo. It describes two control experiments: A quick phenotype assay to determine appropriate experimental conditions, and an immunofluorescence assay to directly assess signaling. Together, these control experiments can help establish a pipeline for using optogenetic tools in early zebrafish embryos. These strategies provide a powerful platform to investigate the roles of signaling in development, health, and physiology.

Indexed as

OptogeneticsZebrafishAnimalsLightProtein DomainsSignal TransductionZebrafish ProteinsZebrafish Proteins

Identifiers

PMID37955383
PMCPMC12284804
OpenAlexW4387968481

What OpenQuestion holds

Textmetadata
LicenceTDM
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.