Haseltine W A, Coffin J M, Hageman T C
J Virol. 1979 Apr;30(1):375-83. doi: 10.1128/JVI.30.1.375-383.1979.
We have investigated the process by which the single-stranded RNA genome of Moloney murine leukemia virus is copied into DNA in vitro. DNA synthesis if initiated near the 5' end of the genome, and the elongation of the growing chain occurs by a jumping mechanism whereby the DNA synthesized at the 5' end of the genome is elongated along the 3' end. Unique DNA fragments synthesized beyond the 5' end of the genome in vitro have, at their 5' and 3' ends, copies of unique sequences from the 5' and 3' ends of the genome. These flank a copy of the 49- to 60-nucleotide terminally redundant sequence. These results indicate that the terminal redundancy serves as a "bridge" to allow a DNA molecule synthesized at the 5' end of the genome to serve as a primer for synthesis from the 3' end.
我们研究了莫洛尼鼠白血病病毒的单链RNA基因组在体外被复制成DNA的过程。DNA合成在基因组的5'端附近起始,生长链的延伸通过一种跳跃机制进行,即基因组5'端合成的DNA沿着3'端延伸。在体外合成的超出基因组5'端的独特DNA片段,在其5'和3'端具有来自基因组5'和3'端的独特序列的拷贝。这些序列位于49至60个核苷酸的末端冗余序列的一个拷贝两侧。这些结果表明,末端冗余充当“桥梁”,使在基因组5'端合成的DNA分子能够作为从3'端进行合成的引物。