McKnight R A, Wall R J, Hennighausen L
Department of Pediatrics, University of Pittsburg School of Medicine, Children's Hospital of Pittsburgh, PA 15213.
Transgenic Res. 1995 Jan;4(1):39-43. doi: 10.1007/BF01976500.
In general, genomic transgenes are expressed efficiently in mice, while their cDNA-based transgenes are frequently silent. Clark et al. (1992) have shown that silent cDNA transgenes under the control of the sheep beta-lactoglobulin promoter can be activated after co-injecting them with a genomic sheep beta-lactoglobulin transgene. We have tested the general utility of this concept using mouse whey acidic protein (WAP) transgenes. Here we show that WAP cDNA transgenes are virtually silent in transgenic mice. In contrast, WAP transgenes containing all introns are expressed in approximately 50% of the lines at levels ranging from 1% to more than 100% of the endogenous RNA (McKnight et al., 1992). When a WAP-genomic transgene was co-injected with a WAP-cDNA, basal activation of the cDNA was possible. However, the activity of the WAP-cDNA transgene did not exceed 1% of the WAP-genomic transgene. This suggests that a permissive integration site capable of supporting basal level transcription can be established, but further events are required for full activation of the transgene.
一般来说,基因组转基因在小鼠中能高效表达,而基于cDNA的转基因则常常沉默。克拉克等人(1992年)表明,在绵羊β-乳球蛋白启动子控制下的沉默cDNA转基因,与基因组绵羊β-乳球蛋白转基因共注射后可被激活。我们使用小鼠乳清酸性蛋白(WAP)转基因测试了这一概念的普遍适用性。在此我们表明,WAP cDNA转基因在转基因小鼠中实际上是沉默的。相比之下,包含所有内含子的WAP转基因在大约50%的品系中表达,表达水平为内源性RNA的1%至超过100%(麦克奈特等人,1992年)。当一个WAP基因组转基因与一个WAP cDNA共注射时,cDNA的基础激活是可能的。然而,WAP cDNA转基因的活性不超过WAP基因组转基因的1%。这表明能够支持基础水平转录的允许整合位点可以建立,但转基因的完全激活还需要进一步的事件。