Jolly D J, Esty A C, Subramani S, Friedmann T, Verma I M
Nucleic Acids Res. 1983 Mar 25;11(6):1855-72. doi: 10.1093/nar/11.6.1855.
We have investigated the effects of long terminal repeats (LTRs) of murine retroviruses on the frequency of obtaining stable transfectants by the herpes virus thymidine kinase (TK) gene. The results indicate that addition of LTRs enhances the number of TK+ transformants by 10-20 fold. A 5-12 fold enhancement was also observed when chromosomal DNA from either human or hamster cells was mixed with a plasmid containing LTR sequences and transfected onto LTR- cells. The LTR sequences involved in the enhancement were localized in the region which contains tandem repeats. All other regions of the LTR did not show any enhancement of stable TK+ transfectants. The location or the orientation of the enhancer sequences with respect to the TK gene did not exert any influence on the frequency of transformation. The enhancement effect does not appear to be linked to either increased numbers of chromosomal integrations or elevated levels of transcription of the TK gene.
我们研究了鼠逆转录病毒的长末端重复序列(LTR)对通过疱疹病毒胸苷激酶(TK)基因获得稳定转染子频率的影响。结果表明,添加LTR可使TK+转化体的数量增加10至20倍。当将来自人或仓鼠细胞的染色体DNA与含有LTR序列的质粒混合并转染到LTR-细胞上时,也观察到了5至12倍的增强。参与增强作用的LTR序列位于包含串联重复序列的区域。LTR的所有其他区域均未显示出稳定的TK+转染子有任何增强。增强子序列相对于TK基因的位置或方向对转化频率没有任何影响。增强作用似乎与染色体整合数量的增加或TK基因转录水平的提高均无关。