Li Ya-Jun, Wei Yu-Sheng, Fu Xiang-Hui, Hao De-Long, Xue Zheng, Gong Huan, Zhang Zhu-Qin, Liu De-Pei, Liang Chih-Chuan
National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Beijing, 100005 China.
J Biol Chem. 2008 Oct 17;283(42):28436-44. doi: 10.1074/jbc.M710289200. Epub 2008 Aug 4.
The apolipoprotein (apo) AI/CIII/AIV/AV cluster genes are expressed at different levels in the liver and intestine. The apoCIII enhancer, a common regulatory element, regulates the tissue-specific expression of apoAI, apoCIII, and apoAIV but not apoAV. To study this regulation at the chromatin level, the histone modifications and intergenic transcription in the human apoAI/CIII/AIV/AV cluster were investigated in HepG2 and Caco-2 cells and in the livers of transgenic mice carrying the human gene cluster constructs with or without the apoCIII enhancer. We found that both the promoters and the intergenic regions of the apoAI/CIII/AIV genes were hyperacetylated and formed an open subdomain that did not include the apoAV gene. Hepatic and intestinal intergenic transcripts were identified to transcribe bidirectionally with strand preferences along the cluster. The deletion of the apoCIII enhancer influenced both histone modification and intergenic transcription in the apoAI/CIII/AIV gene region. These results demonstrate that the apoCIII enhancer contributes to the maintenance of an active chromatin subdomain of the apoAI/CIII/AIV genes, but not apoAV.
载脂蛋白(apo)AI/CIII/AIV/AV基因簇在肝脏和肠道中以不同水平表达。载脂蛋白CIII增强子作为一种常见的调控元件,可调节载脂蛋白AI、载脂蛋白CIII和载脂蛋白AIV的组织特异性表达,但不调节载脂蛋白AV。为了在染色质水平研究这种调控,我们在HepG2和Caco-2细胞以及携带有人基因簇构建体(有或无载脂蛋白CIII增强子)的转基因小鼠肝脏中,研究了人类载脂蛋白AI/CIII/AIV/AV基因簇中的组蛋白修饰和基因间转录。我们发现,载脂蛋白AI/CIII/AIV基因的启动子和基因间区域均发生了高度乙酰化,并形成了一个不包括载脂蛋白AV基因的开放亚结构域。已鉴定出肝脏和肠道的基因间转录本沿基因簇双向转录且具有链偏好性。载脂蛋白CIII增强子的缺失影响了载脂蛋白AI/CIII/AIV基因区域的组蛋白修饰和基因间转录。这些结果表明,载脂蛋白CIII增强子有助于维持载脂蛋白AI/CIII/AIV基因而非载脂蛋白AV的活性染色质亚结构域。