Emerson J A, Vacher J, Cirillo L A, Tilghman S M, Tyner A L
Howard Hughes Medical Institute, Princeton University, New Jersey.
Dev Dyn. 1992 Sep;195(1):55-66. doi: 10.1002/aja.1001950106.
The developmental regulation of the alpha-fetoprotein (AFP) gene in liver results in high-level expression in the fetus, followed by dramatic transcriptional repression after birth. We have examined the mouse AFP gene for transcriptional control sequences that may be involved in its postnatal repression in liver. We showed previously that removal of a DNA region between positions -250 base pairs (bp) and -838 bp of the AFP gene resulted in the persistence of expression of an AFP minigene in the postpartum liver of transgenic mice (Vacher and Tilghman, Science 250:1732-1735, 1990). This study examines the distribution of these transgene transcripts in liver using in situ hybridization. We show that there is a zonal distribution of minigene transcripts in the adult livers of these animals. Hepatocytes surrounding the central veins express high levels of minigene transcripts, while hepatocytes in the intermediate and portal areas contain few, if any, transcripts. Quantitative RNAse protection analysis shows a decrease in transgene RNA levels after birth, consistent with repression in all but a small subset of hepatocytes. These results indicate that repression in the pericentral hepatocytes is dependent upon the presence of a cis-acting, negative-regulatory domain, which is located between the enhancers and the proximal promoter of the AFP gene. In contrast, this domain is not essential for complete repression of AFP transgenes in the intermediate zone and periportal hepatocytes.
肝脏中α-甲胎蛋白(AFP)基因的发育调控导致其在胎儿期高水平表达,出生后转录则受到显著抑制。我们研究了小鼠AFP基因中可能参与其出生后肝脏抑制的转录控制序列。我们之前表明,去除AFP基因中位于-250碱基对(bp)至-838 bp之间的DNA区域,会导致转基因小鼠产后肝脏中AFP小基因的表达持续存在(Vacher和Tilghman,《科学》250:1732 - 1735,1990)。本研究使用原位杂交技术检测了这些转基因转录本在肝脏中的分布。我们发现这些动物成年肝脏中存在小基因转录本的区域分布。中央静脉周围的肝细胞表达高水平的小基因转录本,而中间区域和门静脉区域的肝细胞即使有也很少含有转录本。定量核糖核酸酶保护分析表明出生后转基因RNA水平下降,这与除一小部分肝细胞外所有肝细胞中的抑制情况一致。这些结果表明,中央周围肝细胞中的抑制依赖于位于AFP基因增强子和近端启动子之间的顺式作用负调控结构域的存在。相比之下,该结构域对于中间区域和门静脉周围肝细胞中AFP转基因的完全抑制并非必需。