Webb M L, Maguire K A, Jacob S T
Department of Pharmacology, Pennsylvania State University, College of Medicine, Hershey 17033.
Nucleic Acids Res. 1987 Oct 26;15(20):8547-60. doi: 10.1093/nar/15.20.8547.
The requirement for ATP hydrolysis in the initiation of RNA polymerase II (Pol II)-directed transcription and the relationship between ATP and novobiocin action led us to investigate whether novobiocin could inhibit transcription of the mouse metallothionein-I (MT-I) gene. Novobiocin inhibited the MT-I gene transcription in a fractionated rat hepatoma nuclear extract in a dose-dependent manner by direct interaction with a nuclear factor(s). This interaction prevented formation of stable preinitiation complexes but did not affect elongation of MT-I mRNA. Preincubation of the nuclear extract with ATP prevented the action of novobiocin on MT-I gene transcription. Although novobiocin is known to inhibit DNA topoisomerase II, VM-26, a specific inhibitor of this enzyme had no effect on the transcription. These results indicate that novobiocin blocks the Pol II-directed transcription by inhibiting formation of preinitiation complexes at an ATP-dependent step.
RNA聚合酶II(Pol II)介导的转录起始过程中对ATP水解的需求以及ATP与新生霉素作用之间的关系,促使我们研究新生霉素是否能够抑制小鼠金属硫蛋白-I(MT-I)基因的转录。新生霉素通过与一种核因子直接相互作用,以剂量依赖的方式抑制了大鼠肝癌细胞核提取物中的MT-I基因转录。这种相互作用阻止了稳定的起始前复合物的形成,但不影响MT-I mRNA的延伸。用ATP对核提取物进行预孵育可阻止新生霉素对MT-I基因转录的作用。尽管已知新生霉素可抑制DNA拓扑异构酶II,但该酶的特异性抑制剂VM-26对转录没有影响。这些结果表明,新生霉素通过在ATP依赖步骤抑制起始前复合物的形成来阻断Pol II介导的转录。