Evidence map›Paper›PMID 28678579›Full record

ArticleJournal of neurogenetics2017

Heritable natural variation of an anxiety-like behavior in larval zebrafish.

Mahendra Wagle, Juliana Nguyen, Shinwoo Lee, Noah Zaitlen, Su Guo

Open access · greenAbstract read
In one paragraph

Article in Journal of neurogenetics, 2017. 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
0.9field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Mahendra Waglea Department of Bioengineering and Therapeutic Sciences, Programs in Human Genetics and Biological Sciences, Wheeler Center for the Neurobiology of Addiction , University of California , San Francisco , CA , USA.ORCID 0000-0003-1802-9330
Juliana Nguyena Department of Bioengineering and Therapeutic Sciences, Programs in Human Genetics and Biological Sciences, Wheeler Center for the Neurobiology of Addiction , University of California , San Francisco , CA , USA.
Shinwoo Leea Department of Bioengineering and Therapeutic Sciences, Programs in Human Genetics and Biological Sciences, Wheeler Center for the Neurobiology of Addiction , University of California , San Francisco , CA , USA.
Noah Zaitlenb Department of Medicine , University of California , San Francisco , CA , USA.
Su Guoa Department of Bioengineering and Therapeutic Sciences, Programs in Human Genetics and Biological Sciences, Wheeler Center for the Neurobiology of Addiction , University of California , San Francisco , CA , USA.
University of California, San Francisco · US

Funding

Developing tools for understanding neuromodulation of hypothalamic funcR01DA035680 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUO, SU · 2013 to 2017
$1.7M
Richer Models of Asthma Risk: Bridging the Environment-Genetics DivideK25HL121295 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAITLEN, NOAH A · 2014 to 2018
$784k
A novel RNA-guided platform for dissecting cannabinoid signaling in reward circuit developmentR21DA038447 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUO, SU · 2015 to 2016
$383k
NHLBI NIH HHS K25 HL121295NIDA NIH HHS R01 DA035680NIDA NIH HHS R21 DA038447
6 · The paper itself

Abstract

Complex behaviors are often observed at a spectrum in the population, and psychiatric disorders represent extremes of such behavioral spectra. While grasping the underlying cellular and molecular basis of these disorders represents a major challenge, it is believed that studies of complex behaviors in model organisms, where genotyping and phenotyping can be more conveniently carried out and cause-effect relationships can be further discerned, will help address this challenge. Here we report the characterization of a natural dark aversion behavior in larval zebrafish, which is previously shown to be fear or anxiety-associated. Phenotyping ∼200 individuals using a light/dark choice assay uncovered that, while a majority of individuals displayed medium level of dark aversion (mda), a small number of individuals exhibited strong dark aversion (sda), and a third small cohort showed variable dark aversion (vda). Through selective breeding and phenotyping of the next generation, we demonstrated that both the sda and vda traits are heritable, with sda being invariable while vda being highly variable across multiple trials. Additionally, sda appears to be recessive and vda appears to be dominant over the common allele(s) in the population. Moreover, compared to vda, sda showed increased thigmotaxis (preference for the walls in an open field), another measure of anxiety. Together, these findings reveal a naturally heritable variation of anxiety-like behavior in a tractable model organism, thereby laying foundation for future dissection of the underlying molecular and cellular mechanisms.

Indexed as

Disease Models, AnimalAnalysis of VarianceAnimalsAnimals, Genetically ModifiedAnxietyAvoidance LearningChoice BehaviorDark AdaptationEmbryo, NonmammalianFemaleGenotypeLarvaMaleSex FactorsZebrafishZebrafish ProteinsZebrafish ProteinsAnxietycomplex traitheritablelight preferencepopulation geneticsvariationzebrafish

Identifiers

PMID28678579
PMCPMC6051355
OpenAlexW2725668569

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.