In Sickness and in Health: The Role of TRAPP and Associated Proteins in Disease

被引:42
作者
Brunet, Stephanie [1 ]
Sacher, Michael [1 ,2 ]
机构
[1] Concordia Univ, Dept Biol, Montreal, PQ H4B 1R6, Canada
[2] McGill Univ, Dept Anat & Cell Biol, Montreal, PQ H3A 0G4, Canada
基金
加拿大创新基金会; 加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
autophagy; COP I; COP II; disease; endoplasmic reticulum; Golgi; membrane traffic; Rab1; sedlin; SEDT; TRAPP; NF-KAPPA-B; OLIGOMERIC GOLGI-COMPLEX; RECESSIVE INTELLECTUAL DISABILITY; LENTICULO-SUTURAL DYSPLASIA; BETA-BINDING PROTEIN; ALPHA-SYNUCLEIN; ENDOPLASMIC-RETICULUM; PARKINSONS-DISEASE; COPII VESICLES; WOBBLER MOUSE;
D O I
10.1111/tra.12183
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transport protein particle (TRAPP) represents a series of related protein complexes that function in specific stages of inter-organelle traffic. They share a core of subunits that can activate the GTPase Rab1 through a guanine nucleotide exchange factor (GEF) activity and are distinguished by 'accessory' subunits giving each complex its distinct function. The subunits are ubiquitously expressed and, thus, mutations in TRAPP subunits would be expected to be embryonic lethal. However, since its discovery, a number of subunits have been found to be mutated in several diverse human disorders suggesting that some of these subunits may have cell-or tissue-specific functions. Here we review the current state of knowledge with respect to TRAPP subunit mutations in human disease. We suggest ideas to explain their tissue-specific phenotypes and present avenues for future investigation.
引用
收藏
页码:803 / 818
页数:16
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