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Structural and mechanistic basis of mammalian Nudt12 RNA deNADding.


ABSTRACT: We recently demonstrated that mammalian cells harbor nicotinamide adenine dinucleotide (NAD)-capped messenger RNAs that are hydrolyzed by the DXO deNADding enzyme. Here, we report that the Nudix protein Nudt12 is a second mammalian deNADding enzyme structurally and mechanistically distinct from DXO and targeting different RNAs. The crystal structure of mouse Nudt12 in complex with the deNADding product AMP and three Mg2+ ions at 1.6?Å resolution provides insights into the molecular basis of the deNADding activity in the NAD pyrophosphate. Disruption of the Nudt12 gene stabilizes transfected NAD-capped RNA in cells, and its endogenous NAD-capped mRNA targets are enriched in those encoding proteins involved in cellular energetics. Furthermore, exposure of cells to nutrient or environmental stress manifests changes in NAD-capped RNA levels that are selectively responsive to Nudt12 or DXO, respectively, indicating an association of deNADding to cellular metabolism.

SUBMITTER: Grudzien-Nogalska E 

PROVIDER: S-EPMC6527130 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Structural and mechanistic basis of mammalian Nudt12 RNA deNADding.

Grudzien-Nogalska Ewa E   Wu Yixuan Y   Jiao Xinfu X   Cui Huijuan H   Mateyak Maria K MK   Hart Ronald P RP   Tong Liang L   Kiledjian Megerditch M  

Nature chemical biology 20190517 6


We recently demonstrated that mammalian cells harbor nicotinamide adenine dinucleotide (NAD)-capped messenger RNAs that are hydrolyzed by the DXO deNADding enzyme. Here, we report that the Nudix protein Nudt12 is a second mammalian deNADding enzyme structurally and mechanistically distinct from DXO and targeting different RNAs. The crystal structure of mouse Nudt12 in complex with the deNADding product AMP and three Mg<sup>2+</sup> ions at 1.6 Å resolution provides insights into the molecular ba  ...[more]

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