Suppr超能文献

急性乙醇会改变大脑皮层中模型基因启动子处的多种组蛋白修饰。

Acute ethanol alters multiple histone modifications at model gene promoters in the cerebral cortex.

作者信息

Finegersh Andrey, Homanics Gregg E

机构信息

Departments of Anesthesiology and Pharmacology & Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

Alcohol Clin Exp Res. 2014 Jul;38(7):1865-73. doi: 10.1111/acer.12465. Epub 2014 Jun 18.

Abstract

BACKGROUND

Ethanol (EtOH) exposure alters gene expression in the cerebral cortex (CCx); however, mechanisms of EtOH-induced gene regulation are not well understood. We hypothesized that EtOH regulates gene expression by differentially altering histone modifications at gene promoters that are up- and down-regulated by EtOH. Such epigenetic mechanisms may ultimately contribute to EtOH-induced neuro-adaptations that underlie tolerance, dependence, and EtOH-use disorders.

METHODS

Eight-week-old, male C57BL/6J mice were treated with 3 g/kg EtOH (intraperitoneally) or saline and sacrificed 6 hours after injection; the CCx and hippocampus (HC) were immediately removed and flash frozen. Chromatin immunoprecipitation was used to study the association of model gene promoters with histone modifications. Western blot was used to detect global changes in the histone modifications studied. We also used a polymerase chain reaction (PCR) array to identify changes in expression of chromatin-modifying enzymes.

RESULTS

In CCx, acute EtOH decreased expression of Gad1, Hdac2, and Hdac11, which was associated with decreased histone acetylation at the Gad1 and Hdac2 promoters; we also identified increased expression of Mt1, Mt2, Egr1, which was associated with increased H3K4me3 levels at the Mt2 promoter and decreased H3K27me3 levels at the Mt1 promoter. We identified an increase in global levels of H3K4me3 in CCx as well as a global increase in H3K9ac and H3K14ac in HC. The PCR array identified decreased expression of Csrp2 bp, Hdac2, and Hdac11 as well as increased expression of Kat2b in CCx.

CONCLUSIONS

Acute EtOH induces chromatin remodeling at model up- and down-regulated genes in CCx. Different patterns of histone modifications at these gene promoters indicate that EtOH may be acting through multiple histone-modifying enzymes to alter gene expression; in particular, differential expression of Kat2b, Hdac2, Hdac11, and Csrp2 bp in CCx may mediate EtOH-induced chromatin remodeling. Additional studies are necessary to determine the relationship between EtOH-induced changes in histone-modifying enzymes, specific EtOH-induced histone modifications, and gene expression.

摘要

背景

乙醇(EtOH)暴露会改变大脑皮质(CCx)中的基因表达;然而,乙醇诱导基因调控的机制尚未完全明确。我们推测,乙醇通过差异性地改变其上调和下调基因启动子处的组蛋白修饰来调控基因表达。这种表观遗传机制最终可能导致乙醇诱导的神经适应性变化,而这些变化是耐受性、依赖性和乙醇使用障碍的基础。

方法

对8周龄雄性C57BL/6J小鼠腹腔注射3 g/kg乙醇或生理盐水,并在注射后6小时处死;立即取出CCx和海马体(HC)并速冻。采用染色质免疫沉淀法研究模型基因启动子与组蛋白修饰的关联。使用蛋白质免疫印迹法检测所研究组蛋白修饰的整体变化。我们还使用聚合酶链反应(PCR)芯片来鉴定染色质修饰酶表达的变化。

结果

在CCx中,急性乙醇降低了Gad1、Hdac2和Hdac11的表达,这与Gad1和Hdac2启动子处组蛋白乙酰化的降低有关;我们还发现Mt1、Mt2、Egr1的表达增加,这与Mt2启动子处H3K4me3水平升高以及Mt1启动子处H3K27me3水平降低有关。我们发现CCx中H3K4me3的整体水平增加,以及HC中H3K9ac和H3K14ac的整体水平增加。PCR芯片鉴定出CCx中Csrp2 bp、Hdac2和Hdac11的表达降低以及Kat2b的表达增加。

结论

急性乙醇诱导CCx中模型上调和下调基因的染色质重塑。这些基因启动子处不同的组蛋白修饰模式表明,乙醇可能通过多种组蛋白修饰酶来改变基因表达;特别是,CCx中Kat2b、Hdac2、Hdac11和Csrp2 bp的差异表达可能介导乙醇诱导的染色质重塑。需要进一步研究以确定乙醇诱导的组蛋白修饰酶变化、特定的乙醇诱导组蛋白修饰与基因表达之间的关系。

相似文献

1
Acute ethanol alters multiple histone modifications at model gene promoters in the cerebral cortex.
Alcohol Clin Exp Res. 2014 Jul;38(7):1865-73. doi: 10.1111/acer.12465. Epub 2014 Jun 18.
4
In Vivo Metabolic Tracing Demonstrates the Site-Specific Contribution of Hepatic Ethanol Metabolism to Histone Acetylation.
Alcohol Clin Exp Res. 2018 Oct;42(10):1909-1923. doi: 10.1111/acer.13843. Epub 2018 Aug 16.
5
Epigenetic mechanisms are involved in the regulation of ethanol consumption in mice.
Int J Neuropsychopharmacol. 2014 Oct 31;18(2):pyu072. doi: 10.1093/ijnp/pyu072.
6
Acute Ethanol Produces Ataxia and Induces Fmr1 Expression via Histone Modifications in the Rat Cerebellum.
Alcohol Clin Exp Res. 2019 Jun;43(6):1191-1198. doi: 10.1111/acer.14044. Epub 2019 May 14.
7
Aberrant histone deacetylase2-mediated histone modifications and synaptic plasticity in the amygdala predisposes to anxiety and alcoholism.
Biol Psychiatry. 2013 Apr 15;73(8):763-73. doi: 10.1016/j.biopsych.2013.01.012. Epub 2013 Feb 26.
9
Ethanol induces epigenetic modulation of prodynorphin and pronociceptin gene expression in the rat amygdala complex.
J Mol Neurosci. 2013 Feb;49(2):312-9. doi: 10.1007/s12031-012-9829-y. Epub 2012 Jun 10.
10
`Up-regulation of histone acetylation induced by social defeat mediates the conditioned rewarding effects of cocaine.
Prog Neuropsychopharmacol Biol Psychiatry. 2016 Oct 3;70:39-48. doi: 10.1016/j.pnpbp.2016.04.016. Epub 2016 May 12.

引用本文的文献

1
Evaluation of Salivary Carcinogenic microR-21 and miR-125a Expression Associated with Alcohol Consumption and Smoking.
Asian Pac J Cancer Prev. 2025 Feb 1;26(2):551-556. doi: 10.31557/APJCP.2025.26.2.551.
2
Decreased voluntary alcohol intake and ventral striatal epigenetic and transcriptional remodeling in male Acss2 KO mice.
Neuropharmacology. 2025 Mar 1;265:110258. doi: 10.1016/j.neuropharm.2024.110258. Epub 2024 Dec 9.
3
Epigenetic drugs and psychedelics as emerging therapies for alcohol use disorder: insights from preclinical studies.
J Neural Transm (Vienna). 2024 May;131(5):525-561. doi: 10.1007/s00702-024-02757-3. Epub 2024 Mar 30.
4
The Impact of Alcohol-Induced Epigenetic Modifications in the Treatment of Alcohol use Disorders.
Curr Med Chem. 2024;31(36):5837-5855. doi: 10.2174/0109298673256937231004093143.
5
Adolescent binge ethanol impacts H3K36me3 regulation of synaptic genes.
Front Mol Neurosci. 2023 Mar 3;16:1082104. doi: 10.3389/fnmol.2023.1082104. eCollection 2023.
7
Histone Methylation Regulation in Neurodegenerative Disorders.
Int J Mol Sci. 2021 Apr 28;22(9):4654. doi: 10.3390/ijms22094654.
9
Epigenetic mechanisms underlying pathobiology of alcohol use disorder.
Curr Pathobiol Rep. 2020 Sep;8(3):61-73. doi: 10.1007/s40139-020-00210-0. Epub 2020 Jul 29.
10
Morphopathological approaches in alcoholism.
Rom J Morphol Embryol. 2020 Apr-Jun;61(2):345-351. doi: 10.47162/RJME.61.2.04.

本文引用的文献

1
Repressive epigenetic changes at the mGlu2 promoter in frontal cortex of 5-HT2A knockout mice.
Mol Pharmacol. 2013 Jun;83(6):1166-75. doi: 10.1124/mol.112.084582. Epub 2013 Mar 18.
2
Blockade of ethanol-induced behavioral sensitization by sodium butyrate: descriptive analysis of gene regulations in the striatum.
Alcohol Clin Exp Res. 2013 Jul;37(7):1143-53. doi: 10.1111/acer.12088. Epub 2013 Mar 12.
3
Aberrant histone deacetylase2-mediated histone modifications and synaptic plasticity in the amygdala predisposes to anxiety and alcoholism.
Biol Psychiatry. 2013 Apr 15;73(8):763-73. doi: 10.1016/j.biopsych.2013.01.012. Epub 2013 Feb 26.
4
Chromatin remodeling--a novel strategy to control excessive alcohol drinking.
Transl Psychiatry. 2013 Feb 19;3(2):e231. doi: 10.1038/tp.2013.4.
5
Histone lysine methylation dynamics: establishment, regulation, and biological impact.
Mol Cell. 2012 Nov 30;48(4):491-507. doi: 10.1016/j.molcel.2012.11.006.
6
Expression of ethanol-induced behavioral sensitization is associated with alteration of chromatin remodeling in mice.
PLoS One. 2012;7(10):e47527. doi: 10.1371/journal.pone.0047527. Epub 2012 Oct 22.
7
Ethanol induces epigenetic modulation of prodynorphin and pronociceptin gene expression in the rat amygdala complex.
J Mol Neurosci. 2013 Feb;49(2):312-9. doi: 10.1007/s12031-012-9829-y. Epub 2012 Jun 10.
9
Changes in histone acetylation in the prefrontal cortex of ethanol-exposed adolescent rats are associated with ethanol-induced place conditioning.
Neuropharmacology. 2012 Jun;62(7):2309-19. doi: 10.1016/j.neuropharm.2012.01.011. Epub 2012 Feb 11.
10
Direct recruitment of polycomb repressive complex 1 to chromatin by core binding transcription factors.
Mol Cell. 2012 Feb 10;45(3):330-43. doi: 10.1016/j.molcel.2011.11.032.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验