Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects.
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Summary
The analysis indicates the requirement for Smn in motoneurons to maintain SV2 in presynaptic terminals indicating that Smn, either directly or indirectly, plays a role in Presynaptic integrity.
- Type
- article
- Published
- 2009-10-01
- Cited by
- 117
- References
- 52
- Access
- Open access
- OpenAlex
- https://openalex.org/W19592581
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:17337196
Keywords
Computer science
References
- The Synaptic Vesicle Protein SV2 Is Complexed with an α5-Containing Laminin on the Nerve Terminal Surface*
- A high-throughput method for identifying N-ethyl-N-nitrosourea (ENU)-induced point mutations in zebrafish.
- Paralytic Zebrafish Lacking Acetylcholine Receptors Fail to Localize Rapsyn Clusters to the Synapse
- An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)
- Identification and characterization of a spinal muscular atrophy-determining gene
- A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.
- Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number.
- Correlation between severity and SMN protein level in spinal muscular atrophy
- Plastin 3 Is a Protective Modifier of Autosomal Recessive Spinal Muscular Atrophy
- SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing.
- Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice
- Identification of a transmembrane glycoprotein specific for secretory vesicles of neural and endocrine cells
- Synaptic Vesicle Protein 2 Enhances Release Probability at Quiescent Synapses
- Ribonucleoprotein Assembly Defects Correlate with Spinal Muscular Atrophy Severity and Preferentially Affect a Subset of Spliceosomal snRNPs
- Transposon tools and methods in zebrafish
- Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy
- SV2 Renders Primed Synaptic Vesicles Competent for Ca2+-Induced Exocytosis
- Smn, the spinal muscular atrophy–determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons
- The Maternal-Zygotic Transition: Death and Birth of RNAs
- SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens
Cited by
- Limited Phenotypic Effects of Selectively Augmenting the SMN Protein in the Neurons of a Mouse Model of Severe Spinal Muscular Atrophy
- Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD.
- Étude des voies de signalisation impliquées dans le contrôle de l’expression de SMN dans des modèles murins d’Amyotrophie Spinale Infantile
- Spinal muscular atrophies.
- The development of zebrafish ( Danio rerio ) as a rapid and efficient model system for therapeutic drug screening for Spinal Muscular Atrophy
- Pathogenetic role of MFN2 gene: genetic analysis in patients with charcot-marie-tooth neuropathy and disease modeling in zebrafish
- Effective heritable gene knockdown in zebrafish using synthetic microRNAs
- Development of Therapies for Spinal Muscular Atrophy Using Gene Therapy and Nanotechnology
- Advances and challenges in developing a therapy for spinal muscular atrophy
- The motor neuron response to SMN1 deficiency in spinal muscular atrophy
- Spinal muscular atrophy: a clinical and research update.
- PTEN Depletion Decreases Disease Severity and Modestly Prolongs Survival in a Mouse Model of Spinal Muscular Atrophy
- The many faces of SMN: deciphering the function critical to spinal muscular atrophy pathogenesis
- Small Molecule Suppressors of Drosophila Kinesin Deficiency Rescue Motor Axon Development in a Zebrafish Model of Spinal Muscular Atrophy
- Plasticity of tyrosine hydroxylase and serotonergic systems in the regenerating spinal cord of adult zebrafish
- Vincristine and bortezomib cause axon outgrowth and behavioral defects in larval zebrafish
- Early Development of the Gonadotropin-Releasing Hormone Neuronal Network in Transgenic Zebrafish
- Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy.
- Kisspeptins Modulate the Biology of Multiple Populations of Gonadotropin-Releasing Hormone Neurons during Embryogenesis and Adulthood in Zebrafish (Danio rerio)
- Axonal Transport Defects in a Mitofusin 2 Loss of Function Model of Charcot-Marie-Tooth Disease in Zebrafish
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