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On-demand utilization of phosphoribosyl pyrophosphate by downstream anabolic pathways
The pentose phosphate pathway (PPP) is critical for anabolism and biomass production. Here we show that the essential function of PPP in yeast is the synthesis of phosphoribosyl pyrophosphate (PRPP) catalyzed by PRPP-synthetase. Using combinations of yeast mutants, we found that a mildly decreased s...
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Published in: | The Journal of biological chemistry 2023-08, Vol.299 (8), p.105011-105011, Article 105011 |
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creator | Pinson, Benoît Moenner, Michel Saint-Marc, Christelle Granger-Farbos, Alexandra Daignan-Fornier, Bertrand |
description | The pentose phosphate pathway (PPP) is critical for anabolism and biomass production. Here we show that the essential function of PPP in yeast is the synthesis of phosphoribosyl pyrophosphate (PRPP) catalyzed by PRPP-synthetase. Using combinations of yeast mutants, we found that a mildly decreased synthesis of PRPP affects biomass production, resulting in reduced cell size, while a more severe decrease ends up affecting yeast doubling time. We establish that it is PRPP itself that is limiting in invalid PRPP-synthetase mutants and that the resulting metabolic and growth defect can be bypassed by proper supplementation of the medium with ribose-containing precursors or by the expression of bacterial or human PRPP-synthetase. In addition, using documented pathologic human hyperactive forms of PRPP-synthetase, we show that intracellular PRPP as well as its derived products can be increased in both human and yeast cells, and we describe the ensuing metabolic and physiological consequences. Finally, we found that PRPP consumption appears to take place “on demand” by the various PRPP-utilizing pathways, as shown by blocking or increasing the flux in specific PRPP-consuming metabolic routes. Overall, our work reveals important similarities between human and yeast for both synthesis and consumption of PRPP. |
doi_str_mv | 10.1016/j.jbc.2023.105011 |
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Here we show that the essential function of PPP in yeast is the synthesis of phosphoribosyl pyrophosphate (PRPP) catalyzed by PRPP-synthetase. Using combinations of yeast mutants, we found that a mildly decreased synthesis of PRPP affects biomass production, resulting in reduced cell size, while a more severe decrease ends up affecting yeast doubling time. We establish that it is PRPP itself that is limiting in invalid PRPP-synthetase mutants and that the resulting metabolic and growth defect can be bypassed by proper supplementation of the medium with ribose-containing precursors or by the expression of bacterial or human PRPP-synthetase. In addition, using documented pathologic human hyperactive forms of PRPP-synthetase, we show that intracellular PRPP as well as its derived products can be increased in both human and yeast cells, and we describe the ensuing metabolic and physiological consequences. Finally, we found that PRPP consumption appears to take place “on demand” by the various PRPP-utilizing pathways, as shown by blocking or increasing the flux in specific PRPP-consuming metabolic routes. Overall, our work reveals important similarities between human and yeast for both synthesis and consumption of PRPP.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1016/j.jbc.2023.105011</identifier><identifier>PMID: 37414150</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biochemistry ; Biochemistry, Molecular Biology ; Life Sciences ; nucleotide biosynthesis ; pentose phosphate pathway ; phosphoribosyl pyrophosphate ; yeast</subject><ispartof>The Journal of biological chemistry, 2023-08, Vol.299 (8), p.105011-105011, Article 105011</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Inc. 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subjects | Biochemistry Biochemistry, Molecular Biology Life Sciences nucleotide biosynthesis pentose phosphate pathway phosphoribosyl pyrophosphate yeast |
title | On-demand utilization of phosphoribosyl pyrophosphate by downstream anabolic pathways |
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