Rothenberg E, Baltimore D
J Virol. 1977 Jan;21(1):168-78. doi: 10.1128/JVI.21.1.168-178.1977.
Conditions have been developed for reverse transcription by detergent-disrupted virions of Moloney murine leukemia virus which permit synthesis of molecules that appear to be complete transcripts of the 35S RNA subunits. At limiting Mg2+ concentration, DNA is synthesized in good yield, up to a maximum size of about 2.4 X 10(6) daltons. DNA larger than 2 X 10(6) daltons, taken from alkaline sucrose gradients, has no detectable self-complementarity and was protected from digestion by S1 nuclease to an extent of 90% by annealing to 70S RNA. All size classes of DNA made in these reactions are primed with RNA, because all are initiated with a pApdAjunction. To produce such long molecules, it is necessary to keep the concentration of Mg2+ in the reaction mixture below the total concentration of deoxyribonucleoside triphosphates. Under these conditions, degradation of the RNA template is minimized. The rate of DNA synthesis is also slowed by 30 to 50%, but products longer than 5,000 nucleotides, which are not found otherwise, are completed between 3 and 6h of reaction.
已经为莫洛尼鼠白血病病毒的去污剂裂解病毒粒子的逆转录开发了条件,该条件允许合成似乎是35S RNA亚基完整转录本的分子。在极限Mg2+浓度下,DNA以良好的产率合成,最大尺寸约为2.4×10(6)道尔顿。从碱性蔗糖梯度中获取的大于2×10(6)道尔顿的DNA没有可检测到的自我互补性,并且通过与70S RNA退火,可在90%的程度上免受S1核酸酶的消化。这些反应中产生的所有大小类别的DNA都以RNA为引物,因为所有DNA都以pApdA连接开始。为了产生如此长的分子,有必要将反应混合物中Mg2+的浓度保持在脱氧核糖核苷三磷酸的总浓度以下。在这些条件下,RNA模板的降解最小化。DNA合成速率也减慢了30%至50%,但在反应3至6小时之间完成了否则无法找到的长度超过5000个核苷酸的产物。