Abstract

NAD(+) is an essential metabolic cofactor involved in various cellular biochemical processes. Nicotinamide riboside (NR) is an endogenously produced key pyridine metabolite that plays important roles in the maintenance of NAD(+) pool. Using a NR-specific cell-based screen, we identified mutants that exhibit altered NR release phenotype. Yeast cells lacking the ORF YCL047C/POF1 release considerably more NR compared with wild type, suggesting that POF1 plays an important role in NR/NAD(+) metabolism. The amino acid sequence of Pof1 indicates that it is a putative nicotinamide mononucleotide adenylyltransferase (NMNAT). Unlike other yeast NMNATs, Pof1 exhibits NMN-specific adenylyltransferase activity. Deletion of POF1 significantly lowers NAD(+) levels and decreases the efficiency of NR utilization, resistance to oxidative stress, and NR-induced life span extension. We also show that NR is constantly produced by multiple nucleotidases and that the intracellular NR pools are likely to be compartmentalized, which contributes to the regulation of NAD(+) homeostasis. Our findings may contribute to the understanding of the molecular basis and regulation of NAD(+) metabolism in higher eukaryotes.

Highlights

  • Factors regulating NADϩ metabolism and homeostasis remain unclear because of the dynamic nature of NADϩ synthesis pathways

  • We found that cells lacking the ORF YCL047C/POF1 displayed strong cross-feeding activity (NR release), indicating altered Nicotinamide riboside (NR) metabolism in this mutant (Fig. 1C)

  • Our genetic screen revealed that deleting POF1 significantly increased NR levels, which suggested a role for Pof1 in NR and NADϩ metabolism

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Summary

Introduction

Factors regulating NADϩ metabolism and homeostasis remain unclear because of the dynamic nature of NADϩ synthesis pathways. YCL047C/POF1 Affects NR Metabolism and Encodes a Putative NMNAT—To identify novel players in the NR/NADϩ metabolic pathway, we exploited the NR release property of yeast cells [12] and carried out a genetic screen to identify mutants that showed altered NR release activity, using the nonessential haploid single gene deletion mutants [20] (Fig. 1B). We found that cells lacking the ORF YCL047C/POF1 displayed strong cross-feeding activity (NR release), indicating altered NR metabolism in this mutant (Fig. 1C).

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