Ribonuclease RNase Z is an evolutionarily conserved deAMPylase

Protein AMPylation is a highly conserved posttranslational modification in which adenosine monophosphate (AMP) is covalently attached to protein substrates. Our studies revealed that the mitochondrial AMPylase, Selenoprotein O (SelO), regulates cellular metabolism and oxidative stress response through AMPylation of key metabolic enzymes. Remarkably, SelO-mediated AMPylation is conserved in bacteria and humans, yet the enzyme that removes the AMP from modified proteins remains unknown. We show that the ribonuclease, RNase Z, is both necessary and sufficient to catalyze deAMPylation of AMPylated substrates. These results establish RNase Z as a moonlighting enzyme with previously unrecognized functional roles beyond tRNA processing, expanding our understanding of its biological significance. Furthermore, identification of an evolutionarily conserved deAMPylase highlights the importance of reversible AMPylation as a biological regulatory mechanism, akin to well-studied post translational modifications such as protein phosphorylation.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-11-20
DOI
https://doi.org/10.1073/pnas.2515155122
Primary Topic
Legionella and Acanthamoeba research
Type
article
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article

Ribonuclease RNase Z is an evolutionarily conserved deAMPylase

Meghomukta Mukherjee, Anju Sreelatha, Krzysztof Pawłowski, Alex Pon et al.
Proceedings of the National Academy of Sciences
Legionella and Acanthamoeba research
article

Ribonuclease RNase Z is an evolutionarily conserved deAMPylase

Meghomukta Mukherjee, Anju Sreelatha, Krzysztof Pawłowski, Alex Pon, Timea Goldberg
article en

Abstract

Protein AMPylation is a highly conserved posttranslational modification in which adenosine monophosphate (AMP) is covalently attached to protein substrates. Our studies revealed that the mitochondrial AMPylase, Selenoprotein O (SelO), regulates cellular metabolism and oxidative stress response through AMPylation of key metabolic enzymes. Remarkably, SelO-mediated AMPylation is conserved in bacteria and humans, yet the enzyme that removes the AMP from modified proteins remains unknown. We show that the ribonuclease, RNase Z, is both necessary and sufficient to catalyze deAMPylation of AMPylated substrates. These results establish RNase Z as a moonlighting enzyme with previously unrecognized functional roles beyond tRNA processing, expanding our understanding of its biological significance. Furthermore, identification of an evolutionarily conserved deAMPylase highlights the importance of reversible AMPylation as a biological regulatory mechanism, akin to well-studied post translational modifications such as protein phosphorylation.

Proceedings of the National Academy of SciencesVol. 122(47)
Southwestern Medical Center (US), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 70%
Legionella and Acanthamoeba research
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Ribonuclease RNase Z is an evolutionarily conserved deAMPylase — Meghomukta Mukherjee, Anju Sreelatha, et al. · Proceedings of the National Academy of Sciences (2025) | TGRS Research Map | TGRS