Odorants are volatile molecules that efficiently carry chemical information, providing one of the main ways for communicating with the environment in all kingdoms of life. In the other hand, mammalian genomes codify for hundreds of olfactory receptors (ORs), e.g. about 400 in human and more than 1000 in mouse, underlying the crucial role of the sense of smell during evolution. Therefore, the olfactory system is capable to discriminate between ~10,000 different odors. The possibility of collecting and compiling information about odorants and their receptors is thus fundamental for a functional characterization of the signaling firing event. OlfactionDB, a manually curated database providing comprehensive information for nearly 400 odorant-receptor interactions at the current state, has been developed for managing information about odorants and their receptors. OlfactionDB is a free publicly database available online from: http://molsim.sci.univr.it/OlfactionDB.
α-synuclein is a small protein that is mainly expressed in the synaptic terminals of nervous tissue. Although its implication in neurodegeneration is well established, the physiological role of α-synuclein remains elusive. Given its involvement in the modulation of synaptic transmission and the emerging role of microtubules at the synapse, the current study aimed at investigating whether α-synuclein becomes involved with this cytoskeletal component at the presynapse. We first analyzed the expression of α-synuclein and its colocalization with α-tubulin in murine brain. Differences were found between cortical and striatal/midbrain areas, with substantia nigra pars compacta and corpus striatum showing the lowest levels of colocalization. Using a proximity ligation assay, we revealed the direct interaction of α-synuclein with α-tubulin in murine and in human brain. Finally, the previously unexplored interaction of the two proteins in vivo at the synapse was disclosed in murine striatal presynaptic boutons through multiple approaches, from confocal spinning disk to electron microscopy. Collectively, our data strongly suggest that the association with tubulin/microtubules might actually be an important physiological function for α-synuclein in the synapse, thus suggesting its potential role in a neuropathological context.
