Crooke S T, Sitz T O, Bannon M, Busch H
Physiol Chem Phys. 1975;7(2):177-90.
Purified nucleolar DNA was markedly degraded at a concentration of 13 mug/ml by bleomycin A2; bleomycin concentrations 20-30 times greater were required to degrade nucleoplasmic DNA. Whole nuclear DNA was degraded to only a small extent at 13 mug/ml but was markedly degraded at higher bleomycin concentrations. Treatment of the various types of DNA with high concentrations of bleomycin A2 produced low molecular weight (approximately 6S) fragments that were no longer sensitive to degradation by bleomycin A2. Hybridization studies demonstrated a loss of ribosomal DNA sequences from nucleolar DNA treated with bleomycin A2 in vitro. Studies on RNA synthesis in Novikoff hepatoma ascites cells in vitro showed there was a decreased uptake of 32Pi into high molecular weight nuclear RNA in the presence of bleomycin A2. These results indicate that nucleolar function is inhibited by a direct effect of bleomycin A2 on nucleolar DNA.
在博来霉素A2浓度为13微克/毫升时,纯化的核仁DNA会显著降解;而降解核质DNA则需要比这高20至30倍的博来霉素浓度。全核DNA在13微克/毫升时仅少量降解,但在更高的博来霉素浓度下会显著降解。用高浓度的博来霉素A2处理各种类型的DNA会产生低分子量(约6S)的片段,这些片段对博来霉素A2的降解不再敏感。杂交研究表明,体外经博来霉素A2处理的核仁DNA中核糖体DNA序列有所丢失。对体外培养的诺维科夫肝癌腹水细胞中RNA合成的研究表明,在存在博来霉素A2的情况下,32P进入高分子量核RNA的摄取量减少。这些结果表明,博来霉素A2对核仁DNA的直接作用会抑制核仁功能。