Identification of Yeast and Human 5-Aminoimidazole-4-carboxamide-1-β-D-ribofuranoside (AICAr) Transporters

被引:20
作者
Ceschin, Johanna [1 ,2 ]
Saint-Marc, Christelle [1 ,2 ]
Laporte, Jean [1 ,2 ]
Labriet, Adrien [1 ,2 ]
Philippe, Chloe [1 ,2 ]
Moenner, Michel [1 ,2 ]
Daignan-Fornier, Bertrand [1 ,2 ]
Pinson, Benoit [1 ,2 ]
机构
[1] Univ Bordeaux, IBGC, UMR 5095 1, F-33077 Bordeaux, France
[2] CNRS, Inst Biochim & Genet Cellulaires, UMR 5095 1, F-33077 Bordeaux, France
关键词
ACTIVATED PROTEIN-KINASE; NICOTINAMIDE RIBOSIDE; GENE-EXPRESSION; SHUTTLE VECTORS; AMP; INHIBITION; PHOSPHORYLATION; SENSITIVITY; AGONISTS; THIAMIN;
D O I
10.1074/jbc.M114.551192
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
5-Aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAr) is the precursor of the active monophosphate form (AICAR), a small molecule with potent anti-proliferative and low energy mimetic properties. The molecular bases for AICAR toxicity at the cellular level are poorly understood. Here, we report the isolation and characterization of several yeast AICAr-hypersensitive mutants. Identification of the cognate genes allowed us to establish that thiamine transporters Thi7 and Thi72 can efficiently take up AICAr under conditions where they are overexpressed. We establish that, under standard growth conditions, Nrt1, the nicotinamide riboside carrier, is the major AICAr transporter in yeast. A study of AICAR accumulation in human cells revealed substantial disparities among cell lines and confirmed that AICAr enters cells via purine nucleoside transporters. Together, our results point to significant differences between yeast and human cells for both AICAr uptake and AICAR accumulation.
引用
收藏
页码:16844 / 16854
页数:11
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