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Lethal Accumulation of Guanylic Nucleotides inSaccharomyces cerevisiae HPT1-Deregulated Mutants
Author(s) -
Annick M. Breton,
Benoı̂t Pinson,
Fanny Coulpier,
MarieFrance Giraud,
Alain Dautant,
Bertrand DaignanFornier
Publication year - 2008
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.107.083295
Subject(s) - nucleotide , biology , saccharomyces cerevisiae , mutant , guanine , hypoxanthine guanine phosphoribosyltransferase , mutation , biochemistry , hypoxanthine , repressor , phosphoribosyltransferase , yeast , extracellular , microbiology and biotechnology , genetics , gene , gene expression , enzyme
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.

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