NUDT5 regulates purine metabolism and thiopurine sensitivity by interacting with PPAT

Cells generate purine nucleotides through de novo purine biosynthesis (DNPB) and purine salvage. Purine salvage represses DNPB to prevent excessive purine nucleotide synthesis through mechanisms that are incompletely understood. We identified Nudix hydrolase 5 (NUDT5) as a DNPB regulator. During purine salvage, NUDT5 suppresses DNPB independently of its catalytic function but rather through interaction with phosphoribosyl pyrophosphate amidotransferase (PPAT), the rate-limiting enzyme in the DNPB pathway. The NUDT5-PPAT interaction promoted PPAT oligomerization, suppressed PPAT's enzymatic activity, and facilitated disassembly of the purinosome, a metabolon that functions in DNPB. Disrupting the NUDT5-PPAT interaction overcame DNPB suppression during purine salvage, permitting excessive DNPB and inducing thiopurine resistance. Therefore, NUDT5 governs the balance between DNPB and salvage to maintain appropriate cellular purine nucleotide concentrations.

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Publication Details

Journal
Science
Published
2025-11-06
DOI
https://doi.org/10.1126/science.adx9717
Citations
1
Primary Topic
Biochemical and Molecular Research
Type
article
Field-Weighted Citation Impact
0.81
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article

NUDT5 regulates purine metabolism and thiopurine sensitivity by interacting with PPAT

Ralph J. DeBerardinis, Phong Nguyen, João S. Patrício, Zeng‐Fu Shang et al.
1 citations
Science
Biochemical and Molecular Research
0.81
article

NUDT5 regulates purine metabolism and thiopurine sensitivity by interacting with PPAT

Ralph J. DeBerardinis, Phong Nguyen, João S. Patrício, Zeng‐Fu Shang, Thomas P. Mathews, Qian Cong, Jui‐Chung Chiang, Tao Dai, Xiangyi Li, Islam Alshamleh, Yuanyuan Zhang, Eliot B. Blatt, Varun Sondhi, Run-Wen Yao, Lauren G. Zacharias, Feng Cai, Zheng Wu, Limei Zhang, Wei‐Min Chen, Jing Zhang, Zhifang Lu, Ling Cai, R. Winston, I. Williams, Mya D Moore, Tamaratare Ogu, Xandria Johnson
article en
1 citations

Abstract

Cells generate purine nucleotides through de novo purine biosynthesis (DNPB) and purine salvage. Purine salvage represses DNPB to prevent excessive purine nucleotide synthesis through mechanisms that are incompletely understood. We identified Nudix hydrolase 5 (NUDT5) as a DNPB regulator. During purine salvage, NUDT5 suppresses DNPB independently of its catalytic function but rather through interaction with phosphoribosyl pyrophosphate amidotransferase (PPAT), the rate-limiting enzyme in the DNPB pathway. The NUDT5-PPAT interaction promoted PPAT oligomerization, suppressed PPAT's enzymatic activity, and facilitated disassembly of the purinosome, a metabolon that functions in DNPB. Disrupting the NUDT5-PPAT interaction overcame DNPB suppression during purine salvage, permitting excessive DNPB and inducing thiopurine resistance. Therefore, NUDT5 governs the balance between DNPB and salvage to maintain appropriate cellular purine nucleotide concentrations.

ScienceVol. 390(6778)
University of Nebraska–Lincoln (US), Children's Medical Center (US), Howard Hughes Medical Institute (US), Southwestern Medical Center (US), Southwestern Medical Center (US), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 22%
Biochemical and Molecular Research
0.81
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