Johnson-Thompson M, Rosenthal L J
Antimicrob Agents Chemother. 1979 Nov;16(5):667-73. doi: 10.1128/AAC.16.5.667.
Simian virus 40 nucleoprotein complexes synthesized in the presence of 5-azacytidine showed small differences in sedimentation rate on neutral sucrose and buoyant density in metrizamide and cesium chloride. Simian virus 40 deoxyribonucleic acid (DNA) I, isolated from the nucleoprotein complexes of drug-treated cultures, was found to band at a higher buoyant density and therefore had a decreased ability to bind ethidium bromide. The data indicated that these molecules were deficient in superhelical turns. Treatment with 5-azacytidine was shown to inhibit protein synthesis, which preceded the inhibition of DNA synthesis. Under the same conditions, protein synthesis was inhibited to a greater degree and occurred much faster than inhibition of DNA syntheses. Upon removal of the drug, resumption of protein and DNA synthesis occurred slowly. It is concluded that the inhibition of simian virus 40 DNA synthesis and the conformational alterations in DNA I isolated from nucleoprotein complexes result from the inhibition of protein synthesis.
在5-氮杂胞苷存在的情况下合成的猴病毒40核蛋白复合物,在中性蔗糖中的沉降速率以及在甲泛影酰胺和氯化铯中的浮力密度显示出微小差异。从经药物处理的培养物的核蛋白复合物中分离出的猴病毒40脱氧核糖核酸(DNA)I,被发现以更高的浮力密度形成条带,因此结合溴化乙锭的能力降低。数据表明这些分子缺乏超螺旋结构。结果显示,5-氮杂胞苷处理会抑制蛋白质合成,且这种抑制先于DNA合成的抑制。在相同条件下,蛋白质合成受到的抑制程度更大,且比DNA合成的抑制发生得更快。去除药物后,蛋白质和DNA合成的恢复缓慢。得出的结论是,猴病毒40 DNA合成的抑制以及从核蛋白复合物中分离出的DNA I的构象改变是由蛋白质合成的抑制导致的。