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Comprehensive review highlights NAT10's roles in RNA modification and protein acetylation across diseases, suggesting therapeutic strategies.
The rapid advances in epigenetic and epitranscriptomic regulatory mechanisms have opened new prospects for precision therapies in various diseases. N-acetyltransferase 10 (NAT10) is currently the only known eukaryotic RNA ac4C acetyltransferase and has also been reported to acetylate multiple protein substrates, regulating diverse physiological processes. In this review, we comprehensively describe the domain organization, structural features and subcellular localization of NAT10. The molecular mechanisms underlying NAT10-mediated RNA ac4C modification and protein acetylation, as well as their biological functions across physiological and pathological contexts, are systematically summarized, with the aim of facilitating its clinical translation. Furthermore, we review the recent advances in NAT10-targeted therapeutic strategies, discuss the potential for combining NAT10-targeted strategies with existing treatment modalities, and propose possible approaches for optimization. By integrating current evidence, this review provides insights into the functions of NAT10 and highlights future research directions for its validation and translational development as a clinical therapeutic target in various diseases. Graphical overview of NAT10 domain organization, RNA ac4C and reported protein-lysine acetylation activities, biological functions across major organ systems, and emerging therapeutic strategies. Since the direct binding between Remodelin and NAT10 remains unconfirmed, relevant effects exerted by this small molecule should be indicated with dashed arrows.
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Zhang et al. (2026) studied this question.
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