Hino Kimihiro, Tsuchiya Kiichiro, Fukao Taro, Kiga Kotaro, Okamoto Ryuichi, Kanai Takanori, Watanabe Mamoru
Department of Gastroenterology and Hepatology, Graduate School, Tokyo Medical and Dental University, Tokyo 113-8519, Japan.
RNA. 2008 Jul;14(7):1433-42. doi: 10.1261/rna.810208. Epub 2008 May 20.
Maintenance of the intestinal epithelium is based on well-balanced molecular mechanisms that confer the stable and continuous supply of specialized epithelial cell lineages from multipotent progenitors. Lineage commitment decisions in the intestinal epithelium system involve multiple regulatory systems that interplay with each other to establish the cellular identities. Here, we demonstrate that the microRNA system could be involved in intestinal epithelial cell differentiation, and that microRNA-194 (miR-194) is highly induced during this process. To investigate this inducible expression mechanism, we identified the genomic structure of the miR-194-2, -192 gene, one of the inducible class of miR-194 parental genes. Furthermore, we identified its transcriptional regulatory region that contains a consensus-binding motif for hepatocyte nuclear factor-1alpha (HNF-1alpha), which is well known as a transcription factor to regulate gene expression in intestinal epithelial cells. By chromatin immunoprecipitation assay and luciferase reporter analysis, we revealed that pri-miR-194-2 expression is controlled by HNF-1alpha, and its consensus binding region is required for the transcription of pri-miR-194-2 in vivo in an intestinal epithelial cell line, Caco-2. Our observations indicate that microRNA genes could be targets of lineage-specific transcription factors and that microRNAs are regulated by a tissue-specific manner in the intestinal epithelium. Therefore, our work suggests that induced expression of these microRNAs have important roles in intestinal epithelium maturation.
肠道上皮的维持基于平衡良好的分子机制,这些机制能确保多能祖细胞稳定且持续地供应特化的上皮细胞谱系。肠道上皮系统中的谱系定向决定涉及多个相互作用的调节系统,以确立细胞身份。在此,我们证明微小RNA系统可能参与肠道上皮细胞分化,且微小RNA - 194(miR - 194)在此过程中被高度诱导。为研究这种诱导表达机制,我们确定了miR - 194 - 2、- 192基因的基因组结构,它是miR - 194亲本基因的可诱导类别之一。此外,我们确定了其转录调控区域,该区域包含肝细胞核因子 - 1α(HNF - 1α)的共有结合基序,HNF - 1α是一种众所周知的在肠道上皮细胞中调节基因表达的转录因子。通过染色质免疫沉淀测定和荧光素酶报告基因分析,我们发现初级miR - 194 - 2的表达受HNF - 1α控制,且其共有结合区域对于肠道上皮细胞系Caco - 2中体内初级miR - 194 - 2的转录是必需的。我们的观察结果表明,微小RNA基因可能是谱系特异性转录因子的靶标,且微小RNA在肠道上皮中以组织特异性方式受到调控。因此,我们的研究表明这些微小RNA的诱导表达在肠道上皮成熟中具有重要作用。