Fuhrman S A, Van Beveren C, Verma I M
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5411-5. doi: 10.1073/pnas.78.9.5411.
We have used a soluble in vitro RNA polymerase II transcription system to define the site of initiation of Moloney murine leukemia viral RNA synthesis. Molecularly cloned integrated and unintegrated Moloney murine leukemia virus DNAs were used as templates. The 5' ends of in vitro transcripts and virion RNA of Moloney murine leukemia virus were compared by nuclease S1 protection experiments. Our results indicate that viral sequences upstream of the in vivo cap site are implicated in the transcription of viral RNA and that the 5' end of an in vitro transcript derived from an integrated Moloney murine leukemia virus clone corresponds to the 5' end of viral genomic RNA.
我们使用了一种可溶性体外RNA聚合酶II转录系统来确定莫洛尼鼠白血病病毒RNA合成的起始位点。分子克隆的整合型和未整合型莫洛尼鼠白血病病毒DNA被用作模板。通过核酸酶S1保护实验比较了莫洛尼鼠白血病病毒体外转录本和病毒粒子RNA的5'末端。我们的结果表明,体内帽位点上游的病毒序列与病毒RNA的转录有关,并且来自整合型莫洛尼鼠白血病病毒克隆的体外转录本的5'末端与病毒基因组RNA的5'末端相对应。