Spear B T
Departments of Microbiology and Immunology and Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY 40536-0084, USA.
Semin Cancer Biol. 1999 Apr;9(2):109-16. doi: 10.1006/scbi.1998.0087.
The mouse alpha-fetoprotein (AFP) gene provides an excellent model system to study developmental gene activation and different aspects of liver-specific transcriptional control. AFP is activated early in hepatogenesis, repressed post-natally, and can be reactivated during liver regeneration and in hepatocellular carcinomas. Transgenic studies have also revealed that AFP enhancers, when linked individually to a heterologous promoter, can confer zonal control in the adult liver. Continued transgenic studies, combined with analysis using in vitro and tissue culture systems, will help elucidate mechanisms of transcriptional regulation during liver development and hepatocarcinogenesis.
小鼠甲胎蛋白(AFP)基因提供了一个出色的模型系统,用于研究发育过程中的基因激活以及肝脏特异性转录调控的不同方面。AFP在肝脏发生早期被激活,出生后受到抑制,并且在肝脏再生和肝细胞癌中可被重新激活。转基因研究还表明,AFP增强子单独与异源启动子相连时,可在成年肝脏中赋予区域控制。持续的转基因研究,结合体外和组织培养系统的分析,将有助于阐明肝脏发育和肝癌发生过程中的转录调控机制。