Boone L R, Skalka A M
J Virol. 1981 Jan;37(1):109-16. doi: 10.1128/JVI.37.1.109-116.1981.
We have examined the kinetics of synthesis of minus [(-)]- and plus [(+)]-strand viral DNA in melittin-permeabilized avian retrovirus particles. The reaction was biphasic. There was a very rapid initial rate, followed, after approximately 1 h, by a lower rate. Many discrete bands of subgenomic-length (-) strands were produced after 10 and 20 min of synthesis; genome-length (7.7-kilobase [kb]) (-) strands were detected within 30 min. Extension to an 8.0-kb (-)-strand species was evident by 60 min. This extension was inhibited by actinomycin D. Synthesis of (+) strands (which is also inhibited by actinomycin D) began early, before any (-) strands were completed, and continued for more than 4 h beyond the time when synthesis of full-length DNA had terminated. Two distinct species of (+)-strand DNA, 0.27 and 0.35 kb, could be observed at the earliest times. Their presence was quickly obscured by subsequent formation of (+)-strand molecules of molecular length between 0.2 and 2.0 kb.
我们研究了蜂毒肽通透处理的禽逆转录病毒颗粒中负链[(-)]和正链[(+)]病毒DNA合成的动力学。该反应呈双相性。最初速率非常快,大约1小时后,速率降低。合成10分钟和20分钟后产生了许多亚基因组长度的负链离散条带;30分钟内检测到基因组长度(7.7千碱基[kb])的负链。到60分钟时,延伸至8.0 kb的负链种类明显可见。这种延伸受到放线菌素D的抑制。正链的合成(也受到放线菌素D的抑制)在任何负链完成之前就早早开始,并在全长DNA合成终止后持续超过4小时。最早可观察到两种不同的正链DNA种类,分别为0.27 kb和0.35 kb。它们的存在很快被随后形成的分子长度在0.2至2.0 kb之间的正链分子所掩盖。