METTL3 介导的 lncRNA HNF1A-AS1/HNF4A-AS1 m6A 修饰调节 CYP 的表达。

IF 4.4 3区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Metabolism and Disposition Pub Date : 2024-09-16 DOI:10.1124/dmd.124.001832
Yihang Yu, Jingya Wang, Zaihuan Xiong, Anqi Du, Xiaofei Wang, Yiting Wang, Shengna Han, Pei Wang, Lirong Zhang
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引用次数: 0

摘要

细胞色素 P450 酶(CYPs)表达和活性的个体差异会导致疗效降低或药物不良反应。我们以前曾证实,CYPs 受长非编码 RNA(lncRNA)HNF1A-AS1 和 HNF4A-AS1 的调控,其调控途径是转录因子(TF),包括肝细胞核因子 1a(HNF1A)、肝细胞核因子 4a(HNF4A)和孕烷 X 受体(PXR)。然而,人们对调节 HNF1A-AS1 和 HNF4A-AS1 的上游机制知之甚少。N6-甲基腺苷(m6A)是哺乳动物 RNA 中普遍存在的表转录组修饰。因此,本研究旨在探讨 m6A 修饰是否调控 HNF1A-AS1 和 HNF4A-AS1 的表达,以及是否影响 HepG2 和 Huh7 细胞中 CYP 的表达。甲基转移酶样 3(METTL3)抑制剂 STM2457 能显著抑制 HNF1A-AS1 的表达,并诱导 HNF4A-AS1 的表达。与此相一致的是,细胞系中的 METTL3 功能缺失试验导致 HNF1A-AS1 及其下游 HNF1A、PXR 和 CYPs 在 RNA 水平上下调,以及一些 CYPs 蛋白的下调和 HNF4A-AS1 的上调。功能增益实验的结果显示了相反的趋势。从机理上讲,随后的RNA稳定性实验证实,METTL3影响了这两个lncRNA的稳定性,但影响的方式相反,即METTL3降低了HNF1A-AS1的稳定性,提高了HNF4A-AS1的稳定性。拯救实验证实,METTL3对TFs和CYPs的调控可能需要这两个lncRNA的参与。总之,我们的研究表明,METTL3通过影响HNF1A-AS1/HNF4A-AS1的稳定性参与了TFs介导的CYPs表达。意义声明 虽然lncRNA(HNF1A-AS1和HNF4A-AS1)对下游TF和CYP表达的影响已被充分研究,但METTL3对这两个lncRNA的上游调控仍未被探索。本研究系统研究了METTL3对HepG2和Huh7细胞中lncRNA(HNF1A-AS1和HNF4A-AS1)及其下游TF(HNF1A、HNF4A和PXR)和CYP表达的调控,发现METTL3通过影响HNF1A-AS1和HNF4A-AS1的稳定性参与lncRNA-TF-CYP表达的调控。
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Methyltransferase Like-3-Mediated N6-Methyladenosine Modification of Long Noncoding RNA Hepatocyte Nuclear Factor 1a Antisense RNA 1/Hepatocyte Nuclear Factor 4a Antisense RNA 1 Regulates Cytochrome P450 Enzyme Expression.

Interindividual variations in the expression and activity of cytochrome P450 enzymes (CYPs) led to lower therapeutic efficacy or adverse drug events. We previously demonstrated that CYPs are regulated by the long noncoding RNAs (lncRNAs) hepatocyte nuclear factor 1a antisense RNA 1 (HNF1A-AS1) and HNF4A-AS1 via transcription factors (TFs) including hepatocyte nuclear factor 1a (HNF1A), hepatocyte nuclear factor 4a (HNF4A), and pregnane X receptor (PXR). However, the upstream mechanisms regulating HNF1A-AS1 and HNF4A-AS1 are poorly understood. N6-methyladenosine (m6A) is a prevalent epitranscriptomic modification in mammalian RNA. Therefore, the aim of this study was to investigate whether m6A modification regulates the expression of HNF1A-AS1 and HNF4A-AS1 and affects CYP expression in HepG2 and Huh7 cells. The methyltransferase-like 3 (METTL3) inhibitor, STM2457, significantly suppressed the expression of HNF1A-AS1 and induced HNF4A-AS1 expression. Consistent with this, a loss-of-function assay of METTL3 in the cell lines resulted in the downregulation of HNF1A-AS1 and its downstream HNF1A, PXR, and CYPs at the RNA level, as well as the downregulation of some CYPs proteins, and upregulation of HNF4A-AS1. The results of gain-of-function experiments showed the opposite trend. Mechanistically, subsequent RNA stability experiments confirmed that METTL3 affected the stability of both lncRNAs, but in opposite ways; that is, METTL3 reduced HNF1A-AS1 stability and increased HNF4A-AS1 stability. Rescue experiments confirmed that the regulation of METTL3 on TFs and CYPs may require the involvement of these two lncRNAs. Altogether, our study demonstrates that METTL3 is involved in TFs-mediated CYP expression by affecting HNF1A-AS1/HNF4A-AS1 stability. SIGNIFICANCE STATEMENT: Although the impact of long noncoding RNAs (lncRNAs) including hepatocyte nuclear factor 1a antisense RNA 1 (HNF1A-AS1) and hepatocyte nuclear factor 4a antisense RNA 1 (HNF4A-AS1) on the downstream transcription factor (TF) and cytochrome P450 enzyme (CYP) expression is well studied, the upstream regulation of these two lncRNAs by methyltransferase-like 3 (METTL3) remains unexplored. This study reveals that METTL3 is involved in the regulation of lncRNA-TF-CYP expression by affecting the stability of HNF1A-AS1 and HNF4A-AS1 in HepG2 and Huh7 cells.

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来源期刊
CiteScore
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自引率
12.80%
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期刊介绍: An important reference for all pharmacology and toxicology departments, DMD is also a valuable resource for medicinal chemists involved in drug design and biochemists with an interest in drug metabolism, expression of drug metabolizing enzymes, and regulation of drug metabolizing enzyme gene expression. Articles provide experimental results from in vitro and in vivo systems that bring you significant and original information on metabolism and disposition of endogenous and exogenous compounds, including pharmacologic agents and environmental chemicals.
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