Roth M J, Schwartzberg P L, Goff S P
Department of Biochemistry, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854.
Cell. 1989 Jul 14;58(1):47-54. doi: 10.1016/0092-8674(89)90401-7.
Linear retroviral DNA, the major precursor to the integrated provirus of the murine leukemia viruses, contains a mixture of two structures at its ends: some termini are full-length and blunt, and some have recessed 3' strands. A temporal study of the end structures showed that the proportion of the DNA with recessed ends increases during the course of infection, and suggests that the blunt ends are precursors to the recessed ends. We have examined the DNA structures of the ends of retroviral mutants defective in the integration (IN) function. The results show that the formation of the recessed ends requires the presence of IN. Finally, we have analyzed the structures at the ends of mutant genomes with alterations in the terminal DNA sequence. The exact position of the recessed 3' end can be recessed one, two, or four nucleotides relative to the 5' end. In all cases the position of the recessed 3' end correlates perfectly with, and thus presumably determines, the site of joining to the target DNA.
线性逆转录病毒DNA是鼠白血病病毒整合前病毒的主要前体,其末端含有两种结构的混合物:一些末端是全长且平端的,一些则有凹陷的3'链。对末端结构的时间研究表明,具有凹陷末端的DNA比例在感染过程中增加,这表明平端是凹陷末端的前体。我们已经研究了整合(IN)功能缺陷的逆转录病毒突变体末端的DNA结构。结果表明,凹陷末端的形成需要IN的存在。最后,我们分析了末端DNA序列发生改变的突变基因组末端的结构。凹陷的3'末端相对于5'末端可以凹陷一个、两个或四个核苷酸。在所有情况下,凹陷的3'末端的位置都与靶DNA的连接位点完美相关,因此推测它决定了连接位点。