Hatzoglou M, Lamers W, Bosch F, Wynshaw-Boris A, Clapp D W, Hanson R W
Pew Center for Molecular Nutrition, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.
J Biol Chem. 1990 Oct 5;265(28):17285-93.
Two methods are described for directing the expression of genes to the livers of animals using retroviral vectors containing the predominantly liver-specific promoter from the gene for phosphoenolpyruvate carboxykinase (PEPCK)-linked to the structural gene for either amino 3'-glycosyl phosphotransferase (neo) or bovine growth hormone (bGH). Replication-incompetent retrovirus was used to infect the livers of fetal rats by intraperitoneal injection of animals in utero or to infect adult rats by direct injection into the portal vein after partial hepatectomy. The proviruses were integrated into the hepatic DNA, and the chimeric genes were expressed from the PEPCK promoter for as long as 8 months after infection. The expression of the PEPCK-bGH gene was regulated by diet and hormones in a manner similar to the regulation of the endogenous PEPCK gene in the liver. The potential of this method for targeting genes to the liver is discussed.
本文描述了两种利用逆转录病毒载体将基因定向表达于动物肝脏的方法。这些逆转录病毒载体含有主要来自磷酸烯醇丙酮酸羧激酶(PEPCK)基因的肝脏特异性启动子,并与氨基3'-糖基磷酸转移酶(neo)或牛生长激素(bGH)的结构基因相连。无复制能力的逆转录病毒通过子宫内腹腔注射感染胎鼠肝脏,或在部分肝切除后通过门静脉直接注射感染成年大鼠。前病毒整合到肝脏DNA中,嵌合基因在感染后长达8个月的时间里从PEPCK启动子表达。PEPCK-bGH基因的表达受饮食和激素调节,其方式类似于肝脏中内源性PEPCK基因的调节。本文还讨论了这种将基因靶向肝脏的方法的潜力。