Acetaldehyde-driven mRNA methylation and expression changes in ethanol-metabolizing enzyme genes.

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Epigenetics Pub Date : 2025-12-01 Epub Date: 2025-04-19 DOI:10.1080/15592294.2025.2493865
Ji Sun Koo, Qiansheng Zhan, Huiping Zhang
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引用次数: 0

Abstract

This study examines how the alcohol metabolite acetaldehyde modulates mRNA methylation and expression of ethanol-metabolizing genes, uncovering its epigenetic role in ethanol metabolism. Using neuron-like (SH-SY5Y) and non-neuronal (SW620) cellular models, we examined the effects of chronic intermittent acetaldehyde (CIA) exposure and subsequent withdrawal (CIA+WD) on global RNA m6A modifications and the methylation and expression of three brain ethanol-metabolizing genes: CAT (catalase), CYP2E1 (cytochrome P450 2E1), and ALDH2 (aldehyde dehydrogenase 2). A 3-week CIA exposure, with or without 24-hour withdrawal, did not significantly alter global m6A methylation levels in either cell line. However, acetaldehyde exposure/withdrawal induced hypermethylation at the mRNA stop codon regions of ALDH2 (CIA: p = 0.002; CIA+WD: p = 0.055) and CAT (CIA: p = 0.077; CIA+WD: p = 0.036) in SH-SY5Y cells, but not in SW620 cells. Furthermore, ALDH2 mRNA expression was significantly upregulated in both cell types following exposure (SH-SY5Y: p = 0.073 [CIA] and 0.00002 [CIA+WD]; SW620: p = 0.0009 [CIA] and 0.00008 [CIA+WD]). In contrast, CYP2E1 mRNA methylation and the expression of CYP2E1 and CAT remained unchanged. These findings highlight the cell-specific epigenetic effects of acetaldehyde, particularly its role in modulating mRNA methylation and expression of ALDH2, a key enzyme in alcohol metabolism.

乙醛驱动的mRNA甲基化和乙醇代谢酶基因的表达变化。
本研究探讨了酒精代谢物乙醛如何调节乙醇代谢基因的mRNA甲基化和表达,揭示了其在乙醇代谢中的表观遗传作用。使用神经元样(SH-SY5Y)和非神经元(SW620)细胞模型,我们研究了慢性间歇性乙醛(CIA)暴露和随后的戒断(CIA+WD)对全局RNA m6A修饰以及三种脑乙醇代谢基因:CAT(过氧化氢酶)、CYP2E1(细胞色素P450 2E1)和ALDH2(醛脱氢酶2)的甲基化和表达的影响。暴露于CIA 3周,无论是否有24小时停药,两种细胞系的m6A甲基化水平都没有显著改变。然而,乙醛暴露/戒断诱导ALDH2 mRNA停止密码子区域的超甲基化(CIA: p = 0.002;CIA+WD: p = 0.055)和CAT (CIA: p = 0.077;CIA+WD: p = 0.036)在SH-SY5Y细胞中存在,而在SW620细胞中不存在。此外,暴露后两种细胞类型的ALDH2 mRNA表达均显著上调(SH-SY5Y: p = 0.073 [CIA]和0.00002 [CIA+WD];SW620: p = 0.0009 [CIA]和0.00008 [CIA+WD])。相比之下,CYP2E1 mRNA甲基化以及CYP2E1和CAT的表达保持不变。这些发现强调了乙醛的细胞特异性表观遗传效应,特别是其在调节mRNA甲基化和ALDH2表达中的作用,ALDH2是酒精代谢的关键酶。
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来源期刊
Epigenetics
Epigenetics 生物-生化与分子生物学
CiteScore
6.80
自引率
2.70%
发文量
82
审稿时长
3-8 weeks
期刊介绍: Epigenetics publishes peer-reviewed original research and review articles that provide an unprecedented forum where epigenetic mechanisms and their role in diverse biological processes can be revealed, shared, and discussed. Epigenetics research studies heritable changes in gene expression caused by mechanisms others than the modification of the DNA sequence. Epigenetics therefore plays critical roles in a variety of biological systems, diseases, and disciplines. Topics of interest include (but are not limited to): DNA methylation Nucleosome positioning and modification Gene silencing Imprinting Nuclear reprogramming Chromatin remodeling Non-coding RNA Non-histone chromosomal elements Dosage compensation Nuclear organization Epigenetic therapy and diagnostics Nutrition and environmental epigenetics Cancer epigenetics Neuroepigenetics
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