Evidence map›Paper›PMID 36717082›Full record

ArticleGenes, brain, and behavior2023

Morphological and sensorimotor phenotypes in a zebrafish CHARGE syndrome model are domain-dependent.

Dana R Hodorovich, Patrick M Lindsley, Austen A Berry, Derek F Burton, Kurt C Marsden

Abstract read
In one paragraph

Article in Genes, brain, and behavior, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 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

5 authors.

Dana R HodorovichDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, USA.
Patrick M LindsleyDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, USA.
Austen A BerryDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, USA.
Derek F BurtonDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, USA.
Kurt C MarsdenDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, USA.ORCID 0000-0001-8087-6181

Funding

Cellular and Molecular Mechanisms of Behavioral Dysfunction in a Zebrafish Model of CHARGE SyndromeR21NS120079 · NINDS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MARSDEN, KURT C. · 2021 to 2021
$411k
NINDS NIH HHS R21 NS120079NINDS NIH HHS R21NS120079-01
6 · The paper itself

Abstract

CHARGE syndrome is a heterogeneous disorder characterized by a spectrum of defects affecting multiple tissues and behavioral difficulties such as autism, attention-deficit/hyperactivity disorder, obsessive-compulsive disorder, anxiety, and sensory deficits. Most CHARGE cases arise from de novo, loss-of-function mutations in chromodomain-helicase-DNA-binding-protein-7 (CHD7). CHD7 is required for processes such as neuronal differentiation and neural crest cell migration, but how CHD7 affects neural circuit function to regulate behavior is unclear. To investigate the pathophysiology of behavioral symptoms in CHARGE, we established a mutant chd7 zebrafish line that recapitulates multiple CHARGE phenotypes including ear, cardiac, and craniofacial defects. Using a panel of behavioral assays, we found that chd7 mutants have specific auditory and visual behavior deficits that are independent of defects in sensory structures. Mauthner cell-dependent short-latency acoustic startle responses are normal in chd7 mutants, while Mauthner-independent long-latency responses are reduced. Responses to sudden decreases in light are also reduced in mutants, while responses to sudden increases in light are normal, suggesting that the retinal OFF pathway may be affected. Furthermore, by analyzing multiple chd7 alleles we observed that the penetrance of morphological and behavioral phenotypes is influenced by genetic background but that it also depends on the mutation location, with a chromodomain mutation causing the highest penetrance. This pattern is consistent with analysis of a CHARGE patient dataset in which symptom penetrance was highest in subjects with mutations in the CHD7 chromodomains. These results provide new insight into the heterogeneity of CHARGE and will inform future work to define CHD7-dependent neurobehavioral mechanisms.

Indexed as

CHARGE SyndromeAnimalsDNA-Binding ProteinsMutationPhenotypeReflex, StartleZebrafishDNA-Binding ProteinsbehaviorCHARGE syndromechd7CRISPR/Cas9zebrafish

Identifiers

PMID36717082
PMCPMC10242184

What Socratic holds

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LicenceCC BY-NC
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Registered trials

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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 Socratic graph.