Smith J D, Plump A S, Hayek T, Walsh A, Breslow J L
Laboratory of Biochemical Genetics and Metabolism, Rockefeller University, New York, New York 10021.
J Biol Chem. 1990 Sep 5;265(25):14709-12.
Three separate lines of transgenic mice were created with integrated copies of an 11.1-kilobase pair human DNA fragment containing the apolipoprotein (apo) E gene. The endogenous mouse apoE gene is primarily expressed in the liver with varying levels of expression in other tissues. However, in all three transgenic lines high levels of human apoE mRNA were detected only in the kidney, with lower levels found in the liver and other tissues; despite this profile of human apoE mRNA, human apoE was found in the plasma of the transgenic mice at levels comparable to those found in human plasma. All of the human apoE in the plasma of the transgenic mice was associated with lipoproteins. These results suggest that the domain responsible for the high level of apoE expression in liver lies outside of the microinjected DNA fragment and that an ectopic site of expression of an introduced gene may be permissive for the accumulation of its protein in plasma.
构建了三个独立品系的转基因小鼠,它们整合了一个包含载脂蛋白(apo)E基因的11.1千碱基对的人类DNA片段。内源性小鼠apoE基因主要在肝脏中表达,在其他组织中的表达水平各不相同。然而,在所有三个转基因品系中,仅在肾脏中检测到高水平的人类apoE mRNA,在肝脏和其他组织中水平较低;尽管人类apoE mRNA呈现这种分布情况,但在转基因小鼠的血浆中发现人类apoE的水平与在人类血浆中发现的水平相当。转基因小鼠血浆中的所有人类apoE都与脂蛋白相关。这些结果表明,负责肝脏中apoE高水平表达的结构域位于显微注射的DNA片段之外,并且导入基因的异位表达位点可能有利于其蛋白质在血浆中的积累。