SNARE complex in developmental psychiatry: neurotransmitter exocytosis and beyond

被引:0
作者
Renata Basso Cupertino
Djenifer B. Kappel
Cibele Edom Bandeira
Jaqueline Bohrer Schuch
Bruna Santos da Silva
Diana Müller
Claiton Henrique Dotto Bau
Nina Roth Mota
机构
[1] Instituto de Biociências—Universidade Federal do Rio Grande do Sul,Department of Genetics
来源
Journal of Neural Transmission | 2016年 / 123卷
关键词
SNARE; Development; Psychiatry disorders; ADHD; DEVELOPM.PSYCH;
D O I
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中图分类号
学科分类号
摘要
Multiple biological processes throughout development require intracellular vesicular trafficking, where the SNARE (soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptors) complex plays a major role. The core proteins forming the SNARE complex are SNAP-25 (synaptosomal-associated protein 25), VAMP (vesicle-associated membrane protein) and Syntaxins, besides its regulatory proteins, such as Synaptotagmin. Genes encoding these proteins (SNAP25, VAMP1, VAMP2, STX1A, SYT1 and SYT2) have been studied in relation to psychiatric disorders susceptibility. Here, we review physiological aspects of SNARE complex and genetic association results reported for attention deficit hyperactivity disorder, both in children and adults, autism spectrum disorders, major depressive disorder, bipolar disorder and schizophrenia. Moreover, we included findings from expression, pharmacogenetics and animal model studies regarding these clinical phenotypes. The overall scenario depicted here suggests that the SNARE complex may exert distinct roles throughout development, with age-specific effects of genetic variants in psychiatric disorders. Such perspective should be considered in future studies regarding SNARE complex genes.
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页码:867 / 883
页数:16
相关论文
共 531 条
[91]  
Elfving B(2014)Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders BMC Med 375 372-377
[92]  
Bonefeld BE(2006)The endogenous and reactive depression subtypes revisited: integrative animal and human studies implicate multiple distinct molecular mechanisms underlying major depressive disorder J Am Acad Child Adolesc Psychiatry 114 269-89
[93]  
Rosenberg R(2009)Pharmacogenetics of methylphenidate response in preschoolers with ADHD J Am Acad Child Adolesc Psychiatry 9 801-37
[94]  
Wegener G(2000)An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities Nature 133 68-9286
[95]  
Falbo V(2008)Compartmental specificity of cellular membrane fusion encoded in SNARE proteins Biochem Biophys Res Commun 102 5606-5685
[96]  
Floridia G(2002)Syntaxin 1A is required for normal in utero development Am J Med Genet Part B Neuropsychiatr Genet 317 161-643
[97]  
Gaudi S(2004)Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder Mol Psychiatry 75 371-1084
[98]  
Fanous AH(2005)Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD Am J Med Genet Part B Neuropsychiatr Genet 379 81-458
[99]  
Zhao Z(2005)Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B P Natl Acad Sci USA 1385 26-13
[100]  
Van Den Oord EJCG(2002)Glutamate receptor activation triggers a calcium-dependent and SNARE protein-dependent release of the gliotransmitter Neurosci Lett 22 9278-800