Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.heliyon.2020.e04600
Title: Vesicle transport through interaction with t-SNAREs 1a (Vti1a)'s roles in neurons
Authors: Tang, B.L. 
Keywords: Cellular neuroscience
Gene mutation
Membrane
Molecular neuroscience
Neuron
Neuroscience
Soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE)
VAMP4
VAMP7
Vti1a
Issue Date: 2020
Publisher: Elsevier Ltd
Citation: Tang, B.L. (2020). Vesicle transport through interaction with t-SNAREs 1a (Vti1a)'s roles in neurons. Heliyon 6 (8) : e04600. ScholarBank@NUS Repository. https://doi.org/10.1016/j.heliyon.2020.e04600
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Neuron, Soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE), VAMP4, VAMP7, Vti1a, Neuroscience, Cellular neuroscience, Molecular neuroscience, Membrane, Gene mutation. � 2020 The Author(s)The Soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) family mediates membrane fusion during membrane trafficking and autophagy in all eukaryotic cells, with a number of SNAREs having cell type-specific functions. The endosome-trans-Golgi network (TGN) localized SNARE, Vesicle transport through interaction with t-SNAREs 1A (Vti1a), is unique among SNAREs in that it has numerous neuron-specific functions. These include neurite outgrowth, nervous system development, spontaneous neurotransmission, synaptic vesicle and dense core vesicle secretion, as well as a process of unconventional surface transport of the Kv4 potassium channel. Furthermore, the human VT11A gene is known to form fusion products with neighboring genes in cancer tissues, and VT11A variants are associated with risk in cancers, including glioma. In this review, I highlight VTI1A's known physio-pathological roles in brain neurons, as well as unanswered questions in these regards. � 2020 The Author(s)
Source Title: Heliyon
URI: https://scholarbank.nus.edu.sg/handle/10635/197651
ISSN: 24058440
DOI: 10.1016/j.heliyon.2020.e04600
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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