Dohda Takeaki, Kaneoka Hidenori, Inayoshi Yujin, Kamihira Masamichi, Miyake Katsuhide, Iijima Shinji
Department of Biotechnology, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.
J Biochem. 2004 Sep;136(3):313-9. doi: 10.1093/jb/mvh123.
Transcriptional coactivators, CREB-binding protein (CBP) and p300, exhibit high homology in structure and similar functions. In the present study, we analyzed the function of CBP and p300 proteins as transcriptional coactivators in the expression of albumin in hepatocytes. The expression levels of CBP and p300 were high in fetal hepatocytes, but low in adult ones. Immunoprecipitation assays showed that both CBP and p300 interacted with hepatocyte nuclear factor-1alpha (HNF-1alpha) in primary hepatocytes. Furthermore, CBP and p300 were co-precipitated without HNF-1alpha. Chromatin immunoprecipitation (ChIP) assays revealed that both CBP and p300 are located in the albumin promoter region in hepatocytes. These results suggested that HNF-1alpha, CBP and p300 were incorporated into a preinitiation complex of RNA polymerase II at the albumin promoter. Luciferase reporter assays showed that CBP and p300 cooperatively triggered HNF-1alpha-mediated transcription of the albumin promoter. In addition, inhibition of CBP or p300 using small interfering RNAs (siRNAs) resulted in a reduction in albumin expression. These results suggest that both CBP and p300 are required for enhanced expression of albumin.
转录共激活因子,即CREB结合蛋白(CBP)和p300,在结构上具有高度同源性且功能相似。在本研究中,我们分析了CBP和p300蛋白作为转录共激活因子在肝细胞白蛋白表达中的作用。CBP和p300在胎儿肝细胞中的表达水平较高,但在成体肝细胞中较低。免疫沉淀试验表明,CBP和p300在原代肝细胞中均与肝细胞核因子-1α(HNF-1α)相互作用。此外,CBP和p300在没有HNF-1α的情况下也会被共沉淀。染色质免疫沉淀(ChIP)试验显示,CBP和p300均位于肝细胞白蛋白启动子区域。这些结果表明,HNF-1α、CBP和p300在白蛋白启动子处被纳入RNA聚合酶II的起始前复合物中。荧光素酶报告基因试验表明,CBP和p300协同触发HNF-1α介导的白蛋白启动子转录。此外,使用小干扰RNA(siRNA)抑制CBP或p300会导致白蛋白表达降低。这些结果表明,CBP和p300都是白蛋白增强表达所必需的。