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ADRA1A 基因启动子区域的高甲基化与汉族人群中的阿片类药物使用障碍有关。

Hypermethylation in the promoter region of the ADRA1A gene is associated with opioid use disorder in Han Chinese.

机构信息

Key Laboratory of National Health Commission for Forensic Science, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.

Key Laboratory of National Health Commission for Forensic Science, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China; Bioengineering College, Chongqing University, Chongqing 400044, China.

出版信息

Brain Res. 2022 Oct 15;1793:148050. doi: 10.1016/j.brainres.2022.148050. Epub 2022 Aug 11.

Abstract

Opioid use disorder is a chronic brain disease influenced by genetic and epigenetic factors, accounting for approximately 50% of the liability. Adrenergic signaling is involved in opioid use disorder. To demonstrate the associations between methylation alterations in the alpha-1-adrenergic receptor (ADRA1A) gene and opioid use disorder, in the present study, we first examined and compared the methylation levels of 97 CpG sites in the promoter region of the ADRA1A gene in the peripheral blood in 120 patients with heroin use disorder and 111 healthy controls. Correlations between methylation levels and duration of heroin/methadone use were then analyzed. Finally, the predicted binding transcription factors (TFs) and their target sequences in the promoter region of the ADRA1A gene, which include the selected CpG sites, were screened in the JASPAR database. Our results demonstrated that hypermethylation in the promoter region of the ADRA1A gene in the blood was associated with opioid use disorder. Correlations between methylation levels of several CpG sites and duration of heroin/methadone use were observed. TFs TFAP2A and RUNX1 were predicted to bind to the target sequences, which include the CpG sites selected in the current study, in the promoter region of the ADRA1A gene. Our findings further extend the associations between methylation alterations in the ADRA1A gene and opioid use disorder potentially through mechanisms of gene expression regulations in the ADRA1A gene.

摘要

阿片类使用障碍是一种受遗传和表观遗传因素影响的慢性脑部疾病,约占 50%的易感性。肾上腺素能信号参与阿片类使用障碍。为了证明 ADRA1A 基因启动子区域的甲基化改变与阿片类使用障碍之间的关联,本研究首先在 120 名海洛因使用障碍患者和 111 名健康对照者的外周血中检测并比较了 ADRA1A 基因启动子区域的 97 个 CpG 位点的甲基化水平。然后分析了甲基化水平与海洛因/美沙酮使用时间的相关性。最后,在 JASPAR 数据库中筛选了 ADRA1A 基因启动子区域中包含所选 CpG 位点的预测结合转录因子(TF)及其靶序列。我们的结果表明,血液中 ADRA1A 基因启动子区域的过度甲基化与阿片类使用障碍有关。观察到几个 CpG 位点的甲基化水平与海洛因/美沙酮使用时间之间存在相关性。预测 TFAP2A 和 RUNX1 与 ADRA1A 基因启动子区域的靶序列结合,其中包括本研究中选择的 CpG 位点。我们的研究结果进一步扩展了 ADRA1A 基因甲基化改变与阿片类使用障碍之间的关联,可能通过 ADRA1A 基因表达调控的机制。

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