Evidence map›Paper›PMID 40145591›Full record

ArticleDevelopment (Cambridge, England)2025

Optogenetic control of Nodal signaling patterns.

Harold M McNamara, Alison M Guyer, Bill Z Jia, Vicente J Parot, Caleb D Dobbs, Alexander F Schier, Adam E Cohen, Nathan D Lord

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. 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. Review
  4. Article
  5. Disrupted developmental signaling induces novel transcriptional states.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Luminos: open-source software for bidirectional microscopy.bioRxiv : the preprint server for biology · 2025
    Article
  8. All-optical mapping of CaCell calcium · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Harold M McNamaraLewis Sigler Institute, Princeton University, Princeton, NJ 08540, USA.ORCID 0009-0006-6593-6477
Alison M GuyerDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Bill Z JiaDepartment of Systems Biology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA.
Vicente J ParotInstitute for Biological and Medical Engineering, Pontificia Universidad Católica de Chile, Santiago 7820244, Chile.
Caleb D DobbsDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Alexander F SchierBiozentrum, University of Basel, Basel 4056, Switzerland.
Adam E CohenDepartment of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
Nathan D LordDepartment of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0001-9553-2779

Funding

GENETIC MECHANISMS OF AXIS FORMATION IN VERTEBRATESR01GM056211 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHIER, ALEXANDER F · 1997 to 2015
$5.1M
Genetic Mechanisms of Axis Formation in VertebratesR37GM056211 · NIGMS · HARVARD UNIVERSITY · PI SCHIER, ALEXANDER F · 2016 to 2019
$1.5M
Mechanisms of Morphogen Transport and Interpretation in Early EmbryosR00HD097297 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LORD, NATHAN DALE · 2020 to 2023
$619k
Mechanisms of Morphogen Transport and Interpretation in Early EmbryosK99HD097297 · NICHD · HARVARD UNIVERSITY · PI LORD, NATHAN DALE · 2019 to 2020
$257k
Agencia Nacional de Investigación y Desarrollo Fondo Nacional de Desarrollo Científico y Tecnológico Fondecyt 11231198Eunice Kennedy Shriver National Institute of Child Health and Human Development 5K99HD097297National Science Foundation N00014-18-1-2859NICHD NIH HHS K99 HD097297NICHD NIH HHS R00 HD097297NIGMS NIH HHS GM056211NIGMS NIH HHS R01 GM056211NIGMS NIH HHS R37 GM056211NIH HHS GM056211University of PittsburghU.S. Department of Defense N00014-18-1-2859
6 · The paper itself

Abstract

A crucial step in early embryogenesis is the establishment of spatial patterns of signaling activity. Tools to perturb morphogen signals with high resolution in space and time can help reveal how embryonic cells decode these signals to make appropriate fate decisions. Here, we present new optogenetic reagents and an experimental pipeline for creating designer Nodal signaling patterns in live zebrafish embryos. Nodal receptors were fused to the light-sensitive heterodimerizing pair Cry2/CIB1N, and the type II receptor was sequestered to the cytosol. The improved optoNodal2 reagents eliminate dark activity and improve response kinetics, without sacrificing dynamic range. We adapted an ultra-widefield microscopy platform for parallel light patterning in up to 36 embryos, and demonstrated precise spatial control over Nodal signaling activity and downstream gene expression. Patterned Nodal activation drove precisely controlled internalization of endodermal precursors. Furthermore, we used patterned illumination to generate synthetic signaling patterns in Nodal signaling mutants, rescuing several characteristic developmental defects. This study establishes an experimental toolkit for systematic exploration of Nodal signaling patterns in live embryos.

Indexed as

Nodal ProteinOptogeneticsSignal TransductionZebrafishAnimalsAnimals, Genetically ModifiedCryptochromesEmbryo, NonmammalianGene Expression Regulation, DevelopmentalZebrafish ProteinsCryptochromesNodal ProteinZebrafish ProteinsGastrulationMesendodermal patterningMorphogenNodal signalingOptogeneticsZebrafish

Identifiers

PMID40145591
PMCPMC12070070

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.