Lethal accumulation of guanylic nucleotides in Saccharomyces cerevisiae HPT1-deregulated mutants

被引:19
作者
Breton, Annick [1 ,2 ]
Pinson, Benoit [1 ,2 ]
Coulpier, Fanny [3 ]
Giraud, Marie-France [1 ,2 ]
Dautant, Alain [1 ,2 ]
Daignan-Fornier, Bertrand [1 ,2 ]
机构
[1] CNRS, Inst Biochim & Genet Cellulaires, UMR 5095, F-33077 Bordeaux, France
[2] Univ Victor Segalen Bordeaux 2, Inst Biochim & Genet Cellulaires, F-33077 Bordeaux, France
[3] Ecole Normale Super, IFR36, F-75230 Paris, France
关键词
D O I
10.1534/genetics.107.083295
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Guanylic nucleotide biosynthesis is a conserved and highly regulated process. Drugs reducing GMP synthesis affect the immunological response and mutations enabling guanylic-derivative recycling lead to severe mental retardation. While the effects of decreased GMP synthesis have been well documented, the consequences of GMP overproduction in eukaryotes are poorly understood. In this work, we selected and characterized several mutations making yeast hypoxanthine-guanine phosphoribosyltransferase insensitive to feedback inhibition by GMP. In these mutants, accumulation of guanylic nucleotides can be triggered by addition of extracellular guanine. We show that such an accumulation is highly toxic for yeast cells and results in arrest of proliferation and massive cell death. This growth defect could be partially suppressed by overexpression of Rfx1p, a transcriptional repressor of the DNA damage response pathway. Importantly, neither guanylic nucleotide toxicity nor its suppression by Rfx1p was associated with an alteration of forward mutation frequency.
引用
收藏
页码:815 / 824
页数:10
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