PUBLICATION
A Neurexin2aa deficiency results in axon pathfinding defects and increased anxiety in zebrafish
- Authors
- Koh, A., Tao, S., Jing, G.Y., Chaganty, V., See, K., Purushothaman, K., Orbán, L., Mathuru, A.S., Wohland, T., Winkler, C.
- ID
- ZDB-PUB-201208-31
- Date
- 2020
- Source
- Human molecular genetics 29(23): 3765-3780 (Journal)
- Registered Authors
- Mathuru, Ajay, Winkler, Christoph, Wohland, Thorsten
- Keywords
- none
- MeSH Terms
-
- Animals
- Anxiety/etiology
- Anxiety/metabolism
- Anxiety/pathology*
- Axon Guidance*
- CRISPR-Cas Systems
- Gene Expression Regulation, Developmental*
- Motor Neurons/metabolism
- Motor Neurons/pathology*
- Nerve Tissue Proteins/deficiency*
- Nerve Tissue Proteins/genetics
- Neurogenesis*
- Zebrafish
- Zebrafish Proteins/deficiency*
- Zebrafish Proteins/genetics
- PubMed
- 33276371 Full text @ Hum. Mol. Genet.
Citation
Koh, A., Tao, S., Jing, G.Y., Chaganty, V., See, K., Purushothaman, K., Orbán, L., Mathuru, A.S., Wohland, T., Winkler, C. (2020) A Neurexin2aa deficiency results in axon pathfinding defects and increased anxiety in zebrafish. Human molecular genetics. 29(23):3765-3780.
Abstract
Neurexins are presynaptic transmembrane proteins that control synapse activity and are risk factors for autism spectrum disorder (ASD). Zebrafish, a popular model for behavioral studies, has six neurexin genes, but their functions in embryogenesis and behavior remain largely unknown. We have previously reported that nrxn2a is aberrantly spliced and specifically dysregulated in motor neurons (MNs) in models of Spinal Muscular Atrophy (SMA). In this study, we generated nrxn2aa-/- mutants by CRISPR/Cas9 to understand nrxn2aa function at the zebrafish neuromuscular junction (NMJ) and to determine the effects of its deficiency on adult behavior. Homozygous mutant embryos derived from heterozygous parents did not show obvious defects in axon outgrowth or synaptogenesis of MNs. In contrast, maternal-zygotic (MZ) nrxn2aa-/- mutants displayed extensively branched axons and defective MNs, suggesting a cell-autonomous role for maternally provided nrxn2aa in MN development. Analysis of the NMJs revealed enlarged choice points in MNs of mutant larvae and reduced co-localization of pre- and post-synaptic terminals, indicating impaired synapse formation. Severe early NMJ defects partially recovered in late embryos when mutant transcripts became strongly upregulated. Ultimately, however, the induced defects result in muscular atrophy symptoms in adult MZ mutants. Zygotic homozygous mutants developed normally but displayed increased anxiety at adult stages. Together, our data demonstrate an essential role for maternal nrxn2aa in NMJ synapse establishment, while zygotic nrxn2aa expression appears dispensable for synapse maintenance. The viable nrxn2aa-/- mutant furthermore serves as a novel model to study how an increase in anxiety-like behaviors impacts other deficits.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping