Evidence map›Paper›PMID 36521003›Full record

ArticleCurrent protocols2022

Using NeuroPAL Multicolor Fluorescence Labeling to Identify Neurons in C. elegans.

Emerson R Santiago, Ashish Shelar, Nakeirah T M Christie, Maya R Lewis-Hayre, Michael R Koelle

Open access · greenAbstract read
In one paragraph

Article in Current protocols, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Ectopic transcription due to inherited histone methylation may interfere with the ongoing function of differentiated neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Review
  4. 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 1 institution in 1 country.

Emerson R SantiagoDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut, United States.
Ashish ShelarDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, United States.
Nakeirah T M ChristieDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, United States.
Maya R Lewis-HayreDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut, United States.
Michael R KoelleDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, United States.
Yale University · US

Funding

G PROTEIN SIGNALING IN THE C ELEGANS NERVOUS SYSTEMR01NS036918 · NINDS · YALE UNIVERSITY · PI KOELLE, MICHAEL R · 1998 to 2019
$8.0M
Neuromodulator signaling and activity in the C. elegans egg-laying circuit.R01NS086932 · NINDS · YALE UNIVERSITY · PI Kevin Michael Collins, MICHAEL R KOELLE · 2014 to 2026
$5.2M
The role of a previously undiscovered sensory cilium in the model neural circuit that controls C. elegans egg layingF31NS115315 · NINDS · YALE UNIVERSITY · PI CHRISTIE, NAKEIRAH TASHIARA MATHEWS · 2020 to 2021
$61k
NINDS NIH HHS F31 NS115315NINDS NIH HHS R01 NS036918NINDS NIH HHS R01 NS086932
6 · The paper itself

Abstract

NeuroPAL (Neuronal Polychromatic Atlas of Landmarks) is a recently developed transgene that labels each of the 118 classes of neurons in C. elegans with various combinations of four fluorescent proteins. This neuron-type-specific labeling helps identify neurons that could otherwise be confused with neighboring neurons. Neuron identification enables researchers to combine new data that they generate on a C. elegans neuron with existing datasets on that same neuron, such as its synaptic connections, neurotransmitters, and transcriptome. An impediment to using NeuroPAL, however, is overcoming the steep learning curve for interpreting three-dimensional (3D) fluorescence images of crowded neural ganglia within which different neurons may be similarly colored, some neurons are only very faintly labeled, and the positions of some neurons are variable. Here, we provide protocols that allow researchers to learn to accurately identify neurons within 3D images of NeuroPAL-labeled animals. We provide 3D reference images that illustrate NeuroPAL labeling of each body region, and additional 3D images as training exercises to learn to accurately carry out C. elegans neuron identifications. We also provide tools to annotate images in 3D, and suggest that such 3D annotated images should be the standard for documenting C. elegans neuron identifications for publication. © 2022 Wiley Periodicals LLC. Basic Protocol 1: Using Imaris software to view and annotate images of NeuroPAL-labeled animals in 3D Alternate Protocol: Using FIJI/ImageJ software to view and annotate images of NeuroPAL-labeled animals in 3D Basic Protocol 2: Identifying tail neurons-an introduction to identifying neurons Basic Protocol 3: Identifying midbody neurons Basic Protocol 4: Identifying anterior head neurons Basic Protocol 5: Identifying posterior head neurons Basic Protocol 6: Identifying ventral head and retrovesicular ganglion neurons.

Indexed as

Caenorhabditis elegansNeuronsAnimalsFluorescenceGangliaImaging, Three-DimensionalC. elegans • NeuroPAL • neuron identification

Identifiers

PMID36521003
PMCPMC10257892
OpenAlexW4311782352

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.