• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Distinct methylation patterns in histone H3 at Lys-4 and Lys-9 correlate with up- & down-regulation of genes by ethanol in hepatocytes.组蛋白H3赖氨酸-4和赖氨酸-9位点不同的甲基化模式与乙醇对肝细胞中基因的上调和下调相关。
Life Sci. 2007 Sep 1;81(12):979-87. doi: 10.1016/j.lfs.2007.07.030. Epub 2007 Aug 16.
2
Acetylation of histone H3 at lysine 9 by ethanol in rat hepatocytes.乙醇对大鼠肝细胞中组蛋白H3赖氨酸9位点的乙酰化作用。
Biochem Biophys Res Commun. 2003 Jun 27;306(2):501-4. doi: 10.1016/s0006-291x(03)01040-4.
3
Histone h3 modifications in rat hepatic stellate cells by ethanol.乙醇对大鼠肝星状细胞组蛋白H3的修饰作用
Alcohol Alcohol. 2005 Sep-Oct;40(5):367-72. doi: 10.1093/alcalc/agh170. Epub 2005 Jun 6.
4
Gene-selective histone H3 acetylation in the absence of increase in global histone acetylation in liver of rats chronically fed alcohol.长期摄入酒精的大鼠肝脏中基因选择性组蛋白 H3 乙酰化,而全局组蛋白乙酰化没有增加。
Alcohol Alcohol. 2012 May-Jun;47(3):233-9. doi: 10.1093/alcalc/ags004. Epub 2012 Feb 2.
5
Involvement of histone acetyltransferase (HAT) in ethanol-induced acetylation of histone H3 in hepatocytes: potential mechanism for gene expression.组蛋白乙酰转移酶(HAT)参与乙醇诱导的肝细胞中组蛋白H3乙酰化:基因表达的潜在机制。
Am J Physiol Gastrointest Liver Physiol. 2005 Dec;289(6):G1124-36. doi: 10.1152/ajpgi.00091.2005. Epub 2005 Aug 4.
6
Sequence specificity and role of proximal amino acids of the histone H3 tail on catalysis of murine G9A lysine 9 histone H3 methyltransferase.组蛋白H3尾巴近端氨基酸对小鼠G9A赖氨酸9组蛋白H3甲基转移酶催化作用的序列特异性及作用
Biochemistry. 2005 Oct 4;44(39):12998-3006. doi: 10.1021/bi0509907.
7
Surrogate alcohols and their metabolites modify histone H3 acetylation: involvement of histone acetyl transferase and histone deacetylase.替代醇类及其代谢产物可改变组蛋白H3的乙酰化:组蛋白乙酰转移酶和组蛋白去乙酰化酶的作用
Alcohol Clin Exp Res. 2008 May;32(5):829-39. doi: 10.1111/j.1530-0277.2008.00630.x. Epub 2008 Mar 11.
8
Methylation patterns of histone H3 Lys 4, Lys 9 and Lys 27 in transcriptionally active and inactive Arabidopsis genes and in atx1 mutants.拟南芥转录活跃和不活跃基因以及atx1突变体中组蛋白H3赖氨酸4、赖氨酸9和赖氨酸27的甲基化模式。
Nucleic Acids Res. 2005 Sep 12;33(16):5199-207. doi: 10.1093/nar/gki830. Print 2005.
9
A trans-tail histone code defined by monomethylated H4 Lys-20 and H3 Lys-9 demarcates distinct regions of silent chromatin.由单甲基化的H4赖氨酸-20和H3赖氨酸-9所定义的跨尾部组蛋白密码划分出沉默染色质的不同区域。
J Biol Chem. 2006 May 5;281(18):12760-6. doi: 10.1074/jbc.M513462200. Epub 2006 Mar 3.
10
Histone H4-lysine 20 monomethylation is increased in promoter and coding regions of active genes and correlates with hyperacetylation.组蛋白H4赖氨酸20单甲基化在活性基因的启动子和编码区域增加,并与高乙酰化相关。
J Biol Chem. 2005 Nov 18;280(46):38814-22. doi: 10.1074/jbc.M505563200. Epub 2005 Sep 15.

引用本文的文献

1
Distinct peroxisome populations differentially respond to alcohol-associated hepatic injury.不同的过氧化物酶体群体对酒精相关肝损伤有不同反应。
Mol Biol Cell. 2024 Dec 1;35(12):ar156. doi: 10.1091/mbc.E24-06-0252. Epub 2024 Nov 13.
2
Advances in DNA, histone, and RNA methylation mechanisms in the pathophysiology of alcohol use disorder.酒精使用障碍病理生理学中DNA、组蛋白和RNA甲基化机制的进展。
Adv Drug Alcohol Res. 2023 Feb 15;3:10871. doi: 10.3389/adar.2023.10871. eCollection 2023.
3
Epigenetic Aspects and Prospects in Autoimmune Hepatitis.自身免疫性肝炎的表观遗传学方面及展望。
Front Immunol. 2022 Jun 30;13:921765. doi: 10.3389/fimmu.2022.921765. eCollection 2022.
4
Epigenetics in inflammatory liver diseases: A clinical perspective (Review).炎症性肝病中的表观遗传学:临床视角(综述)
Exp Ther Med. 2022 May;23(5):366. doi: 10.3892/etm.2022.11293. Epub 2022 Apr 4.
5
Epigenetics of alcohol-related liver diseases.酒精性肝病的表观遗传学
JHEP Rep. 2022 Mar 10;4(5):100466. doi: 10.1016/j.jhepr.2022.100466. eCollection 2022 May.
6
Alcohol: basic and translational research; 15th annual Charles Lieber &1st Samuel French satellite symposium.酒精:基础与转化研究;第 15 届查尔斯·利伯与第 1 届塞缪尔·弗伦奇卫星研讨会。
Exp Mol Pathol. 2022 Jun;126:104750. doi: 10.1016/j.yexmp.2022.104750. Epub 2022 Feb 19.
7
Alcohol-Associated Tissue Injury: Current Views on Pathophysiological Mechanisms.酒精相关组织损伤:病理生理机制的当前观点。
Annu Rev Physiol. 2022 Feb 10;84:87-112. doi: 10.1146/annurev-physiol-060821-014008.
8
A large scale mass spectrometry-based histone screening for assessing epigenetic developmental toxicity.基于大规模质谱的组蛋白筛选,用于评估表观遗传发育毒性。
Sci Rep. 2022 Jan 24;12(1):1256. doi: 10.1038/s41598-022-05268-x.
9
Mechanism and Therapeutic Opportunities of Histone Modifications in Chronic Liver Disease.慢性肝病中组蛋白修饰的机制与治疗机遇
Front Pharmacol. 2021 Nov 23;12:784591. doi: 10.3389/fphar.2021.784591. eCollection 2021.
10
The Role of Epigenetic Changes in the Progression of Alcoholic Steatohepatitis.表观遗传变化在酒精性脂肪性肝炎进展中的作用
Front Physiol. 2021 Jul 16;12:691738. doi: 10.3389/fphys.2021.691738. eCollection 2021.

本文引用的文献

1
The role of gut-derived bacterial toxins and free radicals in alcohol-induced liver injury.肠道源性细菌毒素和自由基在酒精性肝损伤中的作用。
J Gastroenterol Hepatol. 1998 Sep;13(S1):S39-S50. doi: 10.1111/jgh.1998.13.s1.39.
2
Epigenetic effects of ethanol on liver and gastrointestinal injury.乙醇对肝脏和胃肠道损伤的表观遗传效应。
World J Gastroenterol. 2006 Sep 7;12(33):5265-71. doi: 10.3748/wjg.v12.i33.5265.
3
Microarray analysis of gene expression in the liver during the urinary ethanol cycle in rats fed ethanol intragastrically at a constant rate.以恒定速率经胃内给予乙醇的大鼠在尿乙醇循环过程中肝脏基因表达的微阵列分析。
Exp Mol Pathol. 2005 Oct;79(2):87-94. doi: 10.1016/j.yexmp.2005.06.006.
4
Involvement of histone acetyltransferase (HAT) in ethanol-induced acetylation of histone H3 in hepatocytes: potential mechanism for gene expression.组蛋白乙酰转移酶(HAT)参与乙醇诱导的肝细胞中组蛋白H3乙酰化:基因表达的潜在机制。
Am J Physiol Gastrointest Liver Physiol. 2005 Dec;289(6):G1124-36. doi: 10.1152/ajpgi.00091.2005. Epub 2005 Aug 4.
5
Genomic imprinting and methylation: epigenetic canalization and conflict.基因组印记与甲基化:表观遗传的定向发育与冲突
Trends Genet. 2005 Jun;21(6):356-65. doi: 10.1016/j.tig.2005.04.005.
6
Pro- and anti-apoptotic roles of c-Jun N-terminal kinase (JNK) in ethanol and acetaldehyde exposed rat hepatocytes.c-Jun氨基末端激酶(JNK)在乙醇和乙醛暴露的大鼠肝细胞中的促凋亡和抗凋亡作用
Eur J Pharmacol. 2005 Jan 31;508(1-3):31-45. doi: 10.1016/j.ejphar.2004.12.006. Epub 2005 Jan 13.
7
Gene expression in the liver of rats fed alcohol by means of intragastric infusion.通过胃内灌注给予酒精的大鼠肝脏中的基因表达。
Alcohol. 2004 May;33(1):17-30. doi: 10.1016/j.alcohol.2004.04.001.
8
A chromosomal memory triggered by Xist regulates histone methylation in X inactivation.由Xist触发的染色体记忆在X染色体失活过程中调节组蛋白甲基化。
PLoS Biol. 2004 Jul;2(7):E171. doi: 10.1371/journal.pbio.0020171. Epub 2004 Jul 13.
9
Molecular aspects of alcohol metabolism: transcription factors involved in early ethanol-induced liver injury.酒精代谢的分子层面:参与早期乙醇诱导肝损伤的转录因子
Annu Rev Nutr. 2004;24:55-78. doi: 10.1146/annurev.nutr.24.012003.132258.
10
Microarray gene analysis of the liver in a rat model of chronic, voluntary alcohol intake.慢性自愿饮酒大鼠模型肝脏的基因芯片分析
Alcohol. 2004 Feb;32(2):113-27. doi: 10.1016/j.alcohol.2003.12.001.

组蛋白H3赖氨酸-4和赖氨酸-9位点不同的甲基化模式与乙醇对肝细胞中基因的上调和下调相关。

Distinct methylation patterns in histone H3 at Lys-4 and Lys-9 correlate with up- & down-regulation of genes by ethanol in hepatocytes.

作者信息

Pal-Bhadra Manika, Bhadra Utpal, Jackson Daniel E, Mamatha Linga, Park Pil-Hoon, Shukla Shivendra D

机构信息

Department of Chemical Biology, Indian Institute of Chemical Technology, Hyderabad-500007, India.

出版信息

Life Sci. 2007 Sep 1;81(12):979-87. doi: 10.1016/j.lfs.2007.07.030. Epub 2007 Aug 16.

DOI:10.1016/j.lfs.2007.07.030
PMID:17826801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2706023/
Abstract

Ethanol induced liver injury is associated with a global change in gene expression but its mechanisms are not known. We studied whether alcohol-induced gene expression is associated with post-translational methylations of histone H3. Primary culture of rat hepatocytes was treated with ethanol (50 or 100 mM) for 24 h and the status of methylation of H3 at lys 4 (H3dimeK4) or lys 9 (H3dimeK9) was monitored by Western blotting using antibodies to dimethylated histone H3 at lys 4 or lys 9. The cells exposed to ethanol showed strikingly opposing behaviors in methylation patterns; H3dimeK9 methylation was decreased whereas H3dimeK4 increased. Similar results were obtained in the interphase nuclei. Their binding on the metaphase chromosomes exhibits distinct site specific pattern of accumulation. Next, chromatin immunoprecipitation of the ethanol treated samples with antibodies for methylated lys 4 or lys 9 histone H3 followed by amplification of the immunoprecipitated DNA, was used to determine their association with the promoters of genes up- or downregulated by ethanol. Lys4 methylation was associated with ethanol upregulated genes (Adh, GST-yc2) whereas lys 9 methylation with downregulated genes (Lsdh, cytP4502c11) demonstrating a difference between these two methylations. These results suggest that exposure of hepatocytes to ethanol changes the expression of several susceptible genes which are associated with site specific modification of dimethylated forms of histone H3 amino termini at their regulatory regions.

摘要

乙醇诱导的肝损伤与基因表达的整体变化有关,但其机制尚不清楚。我们研究了酒精诱导的基因表达是否与组蛋白H3的翻译后甲基化有关。用乙醇(50或100 mM)处理大鼠肝细胞原代培养物24小时,使用针对赖氨酸4或赖氨酸9处二甲基化组蛋白H3的抗体通过蛋白质印迹法监测赖氨酸4(H3dimeK4)或赖氨酸9(H3dimeK9)处H3的甲基化状态。暴露于乙醇的细胞在甲基化模式上表现出明显相反的行为;H3dimeK9甲基化减少而H3dimeK4增加。在间期核中也获得了类似的结果。它们在中期染色体上的结合表现出明显的位点特异性积累模式。接下来,用针对甲基化赖氨酸4或赖氨酸9组蛋白H3的抗体对乙醇处理的样品进行染色质免疫沉淀,然后对免疫沉淀的DNA进行扩增,以确定它们与乙醇上调或下调基因的启动子的关联。赖氨酸4甲基化与乙醇上调基因(Adh、GST-yc2)相关,而赖氨酸9甲基化与下调基因(Lsdh、cytP4502c11)相关,这表明这两种甲基化之间存在差异。这些结果表明,肝细胞暴露于乙醇会改变几个易感基因的表达,这些基因与它们调控区域的组蛋白H3氨基末端二甲基化形式的位点特异性修饰有关。