Quintrell N, Fanshier L, Evans B, Levinson W, Bishop J M
J Virol. 1971 Jul;8(1):17-27. doi: 10.1128/JVI.8.1.17-27.1971.
Purified preparations of Rous sarcoma virus (RSV) contain ribonuclease which is either a constituent of the virion surface or an adsorbed contaminant. Treatment of the virus with nonionic detergent to activate ribonucleic acid (RNA)-dependent deoxyribonucleic acid (DNA) polymerase renders the viral genome susceptible to hydrolysis by the external ribonuclease. The extent of this susceptibility can be substantially reduced by the use of limited amounts of detergent. At a concentration of detergent which provides a maximum initial rate of DNA synthesis, the degradation of endogenous viral RNA results in a reduced yield of high molecular weight DNA: RNA hybrid from the polymerase reaction. Attempts to detect virion-associated deoxyribonuclease, by using a variety of double helical DNA species as substrates, have been unsuccessful, but small amounts of nuclease activity directed against single-stranded DNA may be present in purified virus.
劳氏肉瘤病毒(RSV)的纯化制剂含有核糖核酸酶,它要么是病毒粒子表面的组成成分,要么是吸附的污染物。用非离子去污剂处理病毒以激活依赖核糖核酸(RNA)的脱氧核糖核酸(DNA)聚合酶,会使病毒基因组易于被外部核糖核酸酶水解。通过使用限量的去污剂,这种易感性的程度可大幅降低。在提供最大初始DNA合成速率的去污剂浓度下,内源性病毒RNA的降解导致聚合酶反应中高分子量DNA:RNA杂交体的产量降低。通过使用多种双链DNA作为底物来检测病毒粒子相关的脱氧核糖核酸酶的尝试均未成功,但纯化病毒中可能存在少量针对单链DNA的核酸酶活性。