Dhar V N, Miller D A, Kulkarni A B, Miller O J
Mol Cell Biol. 1987 Mar;7(3):1289-92. doi: 10.1128/mcb.7.3.1289-1292.1987.
Cloned human rRNA gene fragments that included the promoter region were introduced into Chinese hamster dihydrofolate reductase-deficient (dhfr-) cells by cotransformation with a dhfr minigene and amplified by selection for methotrexate resistance. The human ribosomal DNA was transcribed by RNA polymerase II, not RNA polymerase I or III. The metaphase chromosome regions containing the transcriptionally active human ribosomal DNA failed to show silver staining.
将包含启动子区域的克隆人rRNA基因片段与二氢叶酸还原酶小基因共转化,导入中国仓鼠二氢叶酸还原酶缺陷(dhfr-)细胞,并通过选择甲氨蝶呤抗性进行扩增。人核糖体DNA由RNA聚合酶II转录,而非RNA聚合酶I或III。含有转录活性人核糖体DNA的中期染色体区域未显示银染。