Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108608
Title: Visualizing K48 Ubiquitination during Presynaptic Formation By Ubiquitination-Induced Fluorescence Complementation (UiFC)
Authors: Pinto, Maria J. 
Pedro, Joana R. 
Costa, Rui O. 
Almeida, Ramiro D. 
Keywords: ubiquitination; presynaptic terminal; presynaptic differentiation; axon development; lysine 48 polyubiquitin
Issue Date: 2016
Publisher: Frontiers Media S.A.
Project: SFRH/BD/51196/2010 
SFRH/BD/77789/2011 
SFRH/BPD/84593/2012 
PTDC/SAU-NEU/104100/2008 
EXPL/NEU- NMC/0541/2012 
UID/NEU/04539/2013 
Marie Curie Actions—International reintegration Grant,7th Framework programme, EU 
Serial title, monograph or event: Frontiers in Molecular Neuroscience
Volume: 9
Issue: JUNE
Abstract: In recent years, signaling through ubiquitin has been shown to be of great importance for normal brain development. Indeed, fluctuations in ubiquitin levels and spontaneous mutations in (de)ubiquitination enzymes greatly perturb synapse formation and neuronal transmission. In the brain, expression of lysine (K) 48-linked ubiquitin chains is higher at a developmental stage coincident with synaptogenesis. Nevertheless, no studies have so far delved into the involvement of this type of polyubiquitin chains in synapse formation. We have recently proposed a role for polyubiquitinated conjugates as triggering signals for presynaptic assembly. Herein, we aimed at characterizing the axonal distribution of K48 polyubiquitin and its dynamics throughout the course of presynaptic formation. To accomplish so, we used an ubiquitination-induced fluorescence complementation (UiFC) strategy for the visualization of K48 polyubiquitin in live hippocampal neurons. We first validated its use in neurons by analyzing changing levels of polyubiquitin. UiFC signal is diffusely distributed with distinct aggregates in somas, dendrites and axons, which perfectly colocalize with staining for a K48-specific antibody. Axonal UiFC aggregates are relatively stable and new aggregates are formed as an axon grows. Approximately 65% of UiFC aggregates colocalize with synaptic vesicle clusters and they preferentially appear in the axonal domains of axo-somatodendritic synapses when compared to isolated axons. We then evaluated axonal accumulation of K48 ubiquitinated signals in bead-induced synapses. We observed rapid accumulation of UiFC signal and endogenous K48 ubiquitin at the sites of newly formed presynapses. Lastly, we show by means of a microfluidic platform, for the isolation of axons, that presynaptic clustering on beads is dependent on E1-mediated ubiquitination at the axonal level. Altogether, these results indicate that enrichment of K48 polyubiquitin at the site of nascent presynaptic terminals is an important axon-intrinsic event for presynaptic differentiation.
URI: https://hdl.handle.net/10316/108608
ISSN: 1662-5099
DOI: 10.3389/fnmol.2016.00043
Rights: openAccess
Appears in Collections:IIIUC - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais

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