Kim Hye Jin, Seong Je Kyung
Laboratory of Developmental Biology and Genomics, College of Veterinary Medicine, Seoul National University, Seoul 08826; Korea Model Animal Priority Center (KMPC), Seoul 08826, Korea.
Laboratory of Developmental Biology and Genomics, College of Veterinary Medicine, Seoul National University, Seoul 08826; Korea Model Animal Priority Center (KMPC), Seoul 08826; BK21 PLUS Program for Creative Veterinary Science Research and Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University, Seoul 08826; Interdisciplinary Program in Bioinformatics and BIO MAX/N-Bio Institute, Seoul National University, Seoul 08826, Korea.
BMB Rep. 2025 Jun;58(6):269-275.
Exercise is a key driver of metabolic enhancement, and the impact of exercise on methyltransferase-like14 protein (Mettl14)-mediated N-methyladenosine (mA) modification remains unexplored. This study investigates the role of Mettl14 in inguinal white adipose tissue (iWAT) concerning exercise-induced metabolic improvement and its underlying mechanisms. We examined voluntary wheel-running exercise in C57BL/6N mice and Mettl14 heterozygous knockout (HET) mice models. We assessed metabolic phenotyping and molecular responses through body composition analysis, blood profiles, indirect calorimetry, real-time PCR, immunoblotting, and immunohistology. mA levels were significantly elevated in the iWAT of trained mice, a result of increased Mettl14 expression. Additionally, higher Mettl14 levels induced by exercise were positively associated with browning markers in iWAT. Mettl14 HET led to increased weight gain and fat accumulation in a mechanism dependent on mA levels. Furthermore, HET mice demonstrated notable reductions in oxygen consumption and energy expenditure at baseline. mA levels were notably reduced in the iWAT of exercise-induced HET mice, yet the associated metabolic impairment was significantly mitigated. Exercise substantially correlates with enhanced browning and metabolic improvements by modulating mA levels through Mettl14 expression in iWAT. However, this pathway does not critically regulate exercise-induced browning and the enhancement of whole-body metabolism. [BMB Reports 2025; 58(6): 269-275].
运动是代谢增强的关键驱动因素,而运动对甲基转移酶样14蛋白(Mettl14)介导的N-甲基腺苷(mA)修饰的影响尚未得到探索。本研究探讨了Mettl14在腹股沟白色脂肪组织(iWAT)中对运动诱导的代谢改善的作用及其潜在机制。我们在C57BL/6N小鼠和Mettl14杂合敲除(HET)小鼠模型中检测了自愿轮转运动情况。我们通过身体成分分析、血液检测、间接量热法、实时PCR、免疫印迹和免疫组织学评估了代谢表型和分子反应。训练小鼠的iWAT中mA水平显著升高,这是Mettl14表达增加的结果。此外,运动诱导的较高Mettl14水平与iWAT中的褐色化标记物呈正相关。Mettl14 HET导致体重增加和脂肪堆积增加,其机制依赖于mA水平。此外,HET小鼠在基线时的氧气消耗和能量消耗显著降低。运动诱导的HET小鼠的iWAT中mA水平显著降低,但其相关的代谢损伤得到了显著缓解。运动通过调节iWAT中Mettl14的表达来调节mA水平,从而与褐色化增强和代谢改善密切相关。然而,该途径并非运动诱导褐色化和全身代谢增强的关键调节因素。[《BMB报告》2025年;58(6):269 - 275]