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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.

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。

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