Deng T L, Li Y, Johnson L F
Department of Biochemistry, Ohio State University, Columbus 43210.
Nucleic Acids Res. 1989 Jan 25;17(2):645-58. doi: 10.1093/nar/17.2.645.
We previously described the construction of an intronless mouse thymidylate synthase (TS) minigene that has the normal 5' and 3' flanking regions of the gene linked to full length TS cDNA. Transfection of the minigene into ts- hamster V79 cells led to low level expression of normal mouse TS mRNA and protein. In the present study we analyzed the effect of introns on the expression of the TS minigene in transient transfection assays. Inclusion of introns 5 and 6 at their normal locations in the coding region led to an 8-9-fold stimulation of the level of TS and TS mRNA. Almost all of introns 5 and 6 could be deleted without diminishing the stimulatory effect. Inclusion of intron 3 also stimulated the expression of the minigene, although to a lesser extent than introns 5 and 6. However, inclusion of intron 4 had no stimulatory effect. Analysis of minigenes that contained various combinations of introns revealed that the stimulatory effects of the introns were not additive.
我们之前描述了一种无内含子的小鼠胸苷酸合成酶(TS)小基因的构建,该基因具有与全长TS cDNA相连的正常基因5'和3'侧翼区域。将该小基因转染到ts - 仓鼠V79细胞中,导致正常小鼠TS mRNA和蛋白质的低水平表达。在本研究中,我们在瞬时转染实验中分析了内含子对TS小基因表达的影响。在编码区的正常位置包含内含子5和6导致TS和TS mRNA水平有8 - 9倍的刺激。几乎所有的内含子5和6都可以删除而不减弱刺激作用。包含内含子3也刺激了小基因的表达,尽管程度小于内含子5和6。然而,包含内含子4没有刺激作用。对包含各种内含子组合的小基因的分析表明,内含子的刺激作用不是累加的。