Evidence map›Paper›PMID 37256960›Full record

ArticleScience advances2023

An AAV-CRISPR/Cas9 strategy for gene editing across divergent rodent species: Targeting neural oxytocin receptors as a proof of concept.

Arjen J Boender, Marina Boon, H Elliott Albers, Samantha R Eck, Brandon A Fricker, Aubrey M Kelly, Joseph E LeDoux, Simone C Motta, Prerana Shrestha, Jack H Taylor and 3 more

Abstract read
In one paragraph

Article in Science advances, 2023. 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
–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

12 citing papers in PubMed.

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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

13 authors.

Arjen J BoenderCenter for Translational Social Neuroscience, Silvio O. Conte Center for Oxytocin and Social Cognition, Emory National Primate Research Center, Emory University, Atlanta, GA, USA.ORCID 0000-0002-6018-3588
Marina BoonCenter for Translational Social Neuroscience, Silvio O. Conte Center for Oxytocin and Social Cognition, Emory National Primate Research Center, Emory University, Atlanta, GA, USA.ORCID 0000-0003-1367-527X
H Elliott AlbersNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Samantha R EckDepartment of Psychology, University of California, Davis, Davis, CA, USA.
Brandon A FrickerDepartment of Psychology, Emory University, Atlanta, GA, USA.ORCID 0000-0002-6037-814X
Aubrey M KellyDepartment of Psychology, Emory University, Atlanta, GA, USA.ORCID 0000-0002-6013-3943
Joseph E LeDouxCenter for Neural Science, New York University, New York, NY, USA.
Simone C MottaInstitute of Biomedical Sciences, Department of Anatomy, University of São Paulo, São Paulo, SP, Brazil.ORCID 0000-0002-2038-529X
Prerana ShresthaDepartment of Neurobiology and Behavior, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.ORCID 0000-0002-4677-0225
Jack H TaylorNeuroscience Institute, Georgia State University, Atlanta, GA, USA.ORCID 0000-0002-4334-1468
Brian C TrainorDepartment of Psychology, University of California, Davis, Davis, CA, USA.ORCID 0000-0002-4627-5478
Rodrigo Triana-Del RioCenter for Neural Science, New York University, New York, NY, USA.ORCID 0000-0003-2794-6157
Larry J YoungCenter for Translational Social Neuroscience, Silvio O. Conte Center for Oxytocin and Social Cognition, Emory National Primate Research Center, Emory University, Atlanta, GA, USA.ORCID 0000-0003-2044-2239

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
The Impact of Oxytocin on the Neural Representation Social Stimuli P50MH100023 · NIMH · EMORY UNIVERSITY · PI YOUNG, LARRY J · 2013 to 2022
$21.8M
Genetic Regulation of Variability in Brain Oxytocin ReceptorsR01MH112788 · NIMH · EMORY UNIVERSITY · PI YOUNG, LARRY J · 2018 to 2022
$2.5M
Supplement: Oxytocin-department circuits of social approach and vigilanceR01MH121829 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TRAINOR, BRIAN C · 2020 to 2024
$2.0M
Development of viral vector mediated CRISPR/Cas9 editing of the prairie vole oxytocin receptor geneR21MH114151 · NIMH · EMORY UNIVERSITY · PI YOUNG, LARRY J · 2017 to 2018
$491k
Advances in the Study of Social NeuroendocrinologyR21MH109302 · NIMH · GEORGIA STATE UNIVERSITY · PI ALBERS, H. ELLIOTT, HUHMAN, KIM L · 2016 to 2017
$417k
NIH HHS P51 OD011132NIMH NIH HHS P50 MH100023NIMH NIH HHS R01 MH112788NIMH NIH HHS R01 MH121829NIMH NIH HHS R21 MH109302NIMH NIH HHS R21 MH114151
6 · The paper itself

Abstract

A major issue in neuroscience is the poor translatability of research results from preclinical studies in animals to clinical outcomes. Comparative neuroscience can overcome this barrier by studying multiple species to differentiate between species-specific and general mechanisms of neural circuit functioning. Targeted manipulation of neural circuits often depends on genetic dissection, and use of this technique has been restricted to only a few model species, limiting its application in comparative research. However, ongoing advances in genomics make genetic dissection attainable in a growing number of species. To demonstrate the potential of comparative gene editing approaches, we developed a viral-mediated CRISPR/Cas9 strategy that is predicted to target the oxytocin receptor (

Indexed as

CRISPR-Cas SystemsGene EditingAnimalsOxytocinReceptors, OxytocinOxytocinReceptors, Oxytocin

Identifiers

PMID37256960
PMCPMC10413677

What OpenQuestion holds

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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.