Human Equilibrative Nucleoside Transporter-3 (hENT3) Spectrum Disorder Mutations Impair Nucleoside Transport, Protein Localization, and Stability

被引:72
作者
Kang, Nayoung [1 ]
Jun, Ah Hyun [1 ]
Bhutia, Yangzom Doma [1 ]
Kannan, Natarajan [2 ]
Unadkat, Jashvant D. [3 ]
Govindarajan, Rajgopal [1 ]
机构
[1] Univ Georgia, Dept Pharmaceut & Biomed Sci, Athens, GA 30602 USA
[2] Univ Georgia, Dept Biochem & Mol Biol, Athens, GA 30602 USA
[3] Univ Washington, Dept Pharmaceut, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
MEMBRANE-PROTEINS; ESCHERICHIA-COLI; GENE; MITOCHONDRIA; DELTA-F508; GLYCINE; PACKING; RESCUE; FAMILY; CELLS;
D O I
10.1074/jbc.M110.109199
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulating evidence reveals that sole mutations in hENT3 cause a spectrum of human genetic disorders. Among these include H syndrome, characterized by scleroderma, hyperpigmentation, hypertrichosis, hepatomegaly, cardiac abnormalities and musculoskeletal deformities, pigmented hypertrichotic dermatosis with insulin-dependent diabetes syndrome, characterized by autoantibody-negative diabetes mellitus and skin deformities, familial Rosai-Dorfman disease, characterized by short stature, familial histiocytosis and sinus histiocytosis with massive lymphadenopathy (SHML), characterized by severe tissue infiltration of immune cells and swollen lymph nodes. hENT3 spectrum disorders share a common mutation and share overlapping clinical manifestations that display many intriguing resemblances to mitochondrial and lysosomal disorders. Although earlier studies identify hENT3 as a mitochondrial and a lysosomal nucleoside transporter, the precise connections between hENT3 and the pathophysiology of these disorders remain unresolved. In this study, we performed functional and biochemical characterization of these mutations in hENT3. We report severe reductions/losses of hENT3 nucleoside transport functions of hENT3 syndrome mutants. In addition to transport alterations, we provide evidence for possible loss of hENT3 functions in all H and pigmented hypertrichotic dermatosis with insulin-dependent diabetes syndromes due to either mis-trafficking or altered stability of mutant hENT3 proteins.
引用
收藏
页码:28343 / 28352
页数:10
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