Fiser-Littell R M, Hanas J S
J Biol Chem. 1987 Sep 5;262(25):11916-9.
Novobiocin and coumermycin, inhibitors of the B subunit of Escherichia coli DNA gyrase, inhibit the binding of Xenopus transcription factor IIIA (TFIIIA) to the 5 S RNA gene. Nalidixic acid and oxolinic acid, inhibitors of the A subunit of DNA gyrase, have no effect on the TFIIIA-5 S RNA gene interaction. Novobiocin and coumermycin inhibit TFIIIA-dependent DNA renaturation. Novobiocin dissociates TFIIIA.5 S RNA gene complexes and TFIIIA.5 S RNA complexes (7 S particles). Novobiocin induces TFIIIA aggregation, a phenomenon likely to be responsible for the inhibition of TFIIIA-DNA interactions. Novobiocin inhibition of TFIIIA can be reversed by dilution.
新生霉素和香豆霉素是大肠杆菌DNA促旋酶B亚基的抑制剂,它们能抑制非洲爪蟾转录因子IIIA(TFIIIA)与5S RNA基因的结合。萘啶酸和恶喹酸是DNA促旋酶A亚基的抑制剂,对TFIIIA与5S RNA基因的相互作用没有影响。新生霉素和香豆霉素抑制TFIIIA依赖的DNA复性。新生霉素使TFIIIA-5S RNA基因复合物和TFIIIA-5S RNA复合物(7S颗粒)解离。新生霉素诱导TFIIIA聚集,这种现象可能是抑制TFIIIA与DNA相互作用的原因。新生霉素对TFIIIA的抑制作用可通过稀释逆转。