Abstract
We report a random disruption in the mouse genome that resulted in lethal paralysis in homozygous newborns. The disruption blocked expression of neurobeachin, a protein containing a BEACH (beige and Chediak-Higashi) domain implicated in synaptic vesicle trafficking and an AKAP (A-kinase anchor protein) domain linked to localization of cAMP-dependent protein kinase activity. nbea-null mice demonstrated a complete block of evoked synaptic transmission at neuromuscular junctions, whereas nerve conduction, synaptic structure, and spontaneous synaptic vesicle release were completely normal. These findings support an essential role for neurobeachin in evoked neurotransmitter release at neuromuscular junctions and suggest that it plays an important role in synaptic transmission.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Action Potentials / physiology
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Animals
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Animals, Newborn
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Brain / embryology
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Brain / pathology
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Carrier Proteins / biosynthesis
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Carrier Proteins / genetics*
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Carrier Proteins / physiology*
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Cells, Cultured
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Dwarfism / genetics
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Dwarfism / pathology
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Gene Expression
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Genes, Dominant
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Genes, Lethal
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Genes, Recessive
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Homozygote
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Humans
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Membrane Proteins
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Mice
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Mice, Transgenic
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Mutagenesis, Insertional
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Nerve Tissue Proteins / biosynthesis
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Nerve Tissue Proteins / genetics*
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Nerve Tissue Proteins / physiology*
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Neural Conduction / physiology
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Neuromuscular Junction / embryology
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Neuromuscular Junction / physiology*
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Neuromuscular Junction / ultrastructure
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Organ Specificity
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Paralysis / congenital
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Paralysis / genetics
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Phenotype
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RNA, Messenger / analysis
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RNA, Messenger / biosynthesis
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Sequence Analysis, DNA
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Synaptic Transmission / genetics
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Synaptic Transmission / physiology*
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Transgenes
Substances
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Carrier Proteins
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Membrane Proteins
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NBEA protein, human
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Nbea protein, mouse
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Nerve Tissue Proteins
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RNA, Messenger