University of Teramo, Department of Veterinary Medicine, 64100 Teramo, Italy.
University Grenoble-Alpes, CNRS UMR 5309, INSERM U1209, Institute for Advanced Biosciences, 38706 La Tronche, France.
Int J Mol Sci. 2024 Jul 9;25(14):7528. doi: 10.3390/ijms25147528.
Nucleoside diphosphate (NDP) kinases 1 and 2 (NME1/2) are well-characterized enzymes known for their NDP kinase activity. Recently, these enzymes have been shown by independent studies to bind coenzyme A (CoA) or acyl-CoA. These findings suggest a hitherto unknown role for NME1/2 in the regulation of CoA/acyl-CoA-dependent metabolic pathways, in tight correlation with the cellular NTP/NDP ratio. Accordingly, the regulation of NME1/2 functions by CoA/acyl-CoA binding has been described, and additionally, NME1/2 have been shown to control the cellular pathways consuming acetyl-CoA, such as histone acetylation and fatty acid synthesis. NME1/2-controlled histone acetylation in turn mediates an important transcriptional response to metabolic changes, such as those induced following a high-fat diet (HFD). This review discusses the CoA/acyl-CoA-dependent NME1/2 activities and proposes that these enzymes be considered as the first identified carriers of CoA/short-chain acyl-CoAs.
核苷二磷酸激酶 1 和 2(NME1/2)是两种特征明确的酶,其以核苷二磷酸激酶活性而闻名。最近的独立研究表明,这些酶能够结合辅酶 A(CoA)或酰基辅酶 A。这些发现表明 NME1/2 在调节依赖辅酶 A/酰基辅酶 A 的代谢途径方面具有迄今为止未知的作用,与细胞内 NTP/NDP 比值密切相关。因此,已经描述了 CoA/酰基辅酶 A 结合对 NME1/2 功能的调节,并且还表明 NME1/2 能够控制消耗乙酰辅酶 A 的细胞途径,例如组蛋白乙酰化和脂肪酸合成。NME1/2 控制的组蛋白乙酰化反过来介导对代谢变化的重要转录反应,例如高脂肪饮食(HFD)诱导的反应。这篇综述讨论了依赖 CoA/酰基辅酶 A 的 NME1/2 活性,并提出应将这些酶视为第一个被鉴定的 CoA/短链酰基辅酶 A 载体。