Fujiwara T, Mizuuchi K
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
Cell. 1988 Aug 12;54(4):497-504. doi: 10.1016/0092-8674(88)90071-2.
The structure of a presumptive DNA intermediate in the integration of retroviral DNA was studied in a cell-free reaction with exogenously added target DNA. The product made by viral core particles of Moloney murine leukemia virus (Mo-MLV) containing linear viral DNA has a structure consistent with an integration mechanism similar to that observed during bacteriophage Mu transposition. In this intermediate, the 3' ends of the LTR sequences are joined to the target DNA, while the 5' ends of the viral DNA remain unjoined. The 5' ends of the LTR sequences in the intermediate are exactly the same as those found in the unintegrated linear double-stranded viral DNA. This result demonstrates that the linear form of Mo-MLV DNA can integrate directly without prior circularization.
利用外源性添加的靶DNA,在无细胞反应中研究了逆转录病毒DNA整合过程中假定的DNA中间体的结构。含有线性病毒DNA的莫洛尼鼠白血病病毒(Mo-MLV)的病毒核心颗粒产生的产物,其结构与在噬菌体Mu转座过程中观察到的整合机制相似。在这个中间体中,LTR序列的3'端与靶DNA相连,而病毒DNA的5'端仍未连接。中间体中LTR序列的5'端与未整合的线性双链病毒DNA中的5'端完全相同。这一结果表明,Mo-MLV DNA的线性形式可以直接整合,无需事先环化。