Colicelli J, Goff S P
Department of Biochemistry and Molecular Biophysics, Columbia University College of Physicians and Surgeons, New York, New York 10032.
J Virol. 1988 Feb;62(2):633-6. doi: 10.1128/JVI.62.2.633-636.1988.
We have previously described the construction of a mutant of Moloney murine leukemia virus, in594-2, which carries a 2-base-pair insertion in the U5 region of the genome and is partially defective in forming the integrated proviral DNA. We have now recovered a cloned copy of an unusual provirus from rat cells infected with this mutant. The viral genome is flanked by long terminal repeats in inverted orientation, with U3 sequences joined to cellular DNA at both of the outer edges. In addition, the provirus is a recombinant, containing a segment of a VL30 element in inverted orientation in place of the Moloney murine leukemia virus env region. The recovery of this provirus indicates that two U3 regions can be used for viral integration and suggests that there may be no absolute requirement in the reaction for those U5 sequences outside the 13-base-pair inverted repeats.
我们之前描述过莫洛尼鼠白血病病毒的一个突变体in594 - 2的构建,该突变体在基因组的U5区域有一个2碱基对的插入,并且在形成整合的前病毒DNA方面存在部分缺陷。我们现在从感染了这种突变体的大鼠细胞中获得了一个异常前病毒的克隆拷贝。病毒基因组两侧是反向排列的长末端重复序列,U3序列在两个外边缘都与细胞DNA相连。此外,该前病毒是一个重组体,包含一段反向排列的VL30元件,取代了莫洛尼鼠白血病病毒的env区域。这个前病毒的获得表明两个U3区域可用于病毒整合,并提示在该反应中对于13碱基对反向重复序列之外的那些U5序列可能没有绝对要求。