Evidence map›Paper›PMID 38483970›Full record

ArticlePLoS genetics2024

Functional labeling of individualized postsynaptic neurons using optogenetics and trans-Tango in Drosophila (FLIPSOT).

Allison N Castaneda, Ainul Huda, Iona B M Whitaker, Julianne E Reilly, Grace S Shelby, Hua Bai, Lina Ni

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 1 institution in 1 country.

Allison N CastanedaSchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0000-0003-3603-2525
Ainul HudaSchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.
Iona B M WhitakerSchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0009-0003-6099-4051
Julianne E ReillySchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.
Grace S ShelbySchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0009-0006-1046-9189
Hua BaiSchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0000-0003-2143-8821
Lina NiSchool of Neuroscience, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United States of America.ORCID 0000-0003-2155-5155
Virginia Tech · US

Funding

Demonstrate the molecular receptor and functions of dorsal organ warm cells in fliesR01GM140130 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI NI, LINA · 2021 to 2025
$1.7M
Develop functional trans-Tango to identify higher-order neurons with determined functionsR21MH122987 · NIMH · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI NI, LINA · 2020 to 2020
$432k
NIGMS NIH HHS R01 GM140130NIMH NIH HHS R21 MH122987
6 · The paper itself

Abstract

A population of neurons interconnected by synapses constitutes a neural circuit, which performs specific functions upon activation. It is essential to identify both anatomical and functional entities of neural circuits to comprehend the components and processes necessary for healthy brain function and the changes that characterize brain disorders. To date, few methods are available to study these two aspects of a neural circuit simultaneously. In this study, we developed FLIPSOT, or functional labeling of individualized postsynaptic neurons using optogenetics and trans-Tango. FLIPSOT uses (1) trans-Tango to access postsynaptic neurons genetically, (2) optogenetic approaches to activate (FLIPSOTa) or inhibit (FLIPSOTi) postsynaptic neurons in a random and sparse manner, and (3) fluorescence markers tagged with optogenetic genes to visualize these neurons. Therefore, FLIPSOT allows using a presynaptic driver to identify the behavioral function of individual postsynaptic neurons. It is readily applied to identify functions of individual postsynaptic neurons and has the potential to be adapted for use in mammalian circuits.

Indexed as

DrosophilaOptogeneticsAnimalsNeuronsSynapses

Identifiers

PMID38483970
PMCPMC10965055
OpenAlexW4392797149

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.