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Nicotinamide mononucleotide adenylyltransferase maintains active zone structure by stabilizing Bruchpilot
Author(s) -
Zang Shaoyun,
Ali Yousuf O,
Ruan Kai,
Zhai R Grace
Publication year - 2013
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.1038/embor.2012.181
Subject(s) - nicotinamide mononucleotide , ubiquitin , chemistry , active zone , microbiology and biotechnology , proteasome , active site , biochemistry , biology , biophysics , nicotinamide adenine dinucleotide , enzyme , nad+ kinase , vesicle , membrane , synaptic vesicle , gene
Active zones are specialized presynaptic structures critical for neurotransmission. We show that a neuronal maintenance factor, nicotinamide mononucleotide adenylyltransferase (NMNAT), is required for maintaining active zone structural integrity in Drosophila by interacting with the active zone protein, Bruchpilot (BRP), and shielding it from activity‐induced ubiquitin–proteasome‐mediated degradation. NMNAT localizes to the peri‐active zone and interacts biochemically with BRP in an activity‐dependent manner. Loss of NMNAT results in ubiquitination, mislocalization and aggregation of BRP, and subsequent active zone degeneration. We propose that, as a neuronal maintenance factor, NMNAT specifically maintains active zone structure by direct protein–protein interaction.
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