Colicelli J, Goff S P
Cell. 1985 Sep;42(2):573-80. doi: 10.1016/0092-8674(85)90114-x.
Soon after infection, retroviruses synthesize a DNA copy of the genomic RNA and insert that DNA into the cellular genome by recombination at inverted repeat sequences at the termini of the viral genome. We have generated mutations that alter one terminus of the genome of Moloney murine leukemia virus (M-MuLV). Some mutations did not prevent integration of the viral DNA even though the very terminal bases were disrupted. Other mutations had dramatic effects on the efficiency of infection; in these cases the formation of preintegrative DNA was normal but the establishment of the productive provirus was prevented. One of these defective mutants gave rise to a pseudorevertant which differed from the wild type but displayed normal infectivity. An unusual number of bases of viral DNA were removed during the integration reaction carried out by this virus.
感染后不久,逆转录病毒会合成基因组RNA的DNA拷贝,并通过在病毒基因组末端的反向重复序列处进行重组,将该DNA插入细胞基因组。我们已经产生了改变莫洛尼鼠白血病病毒(M-MuLV)基因组一个末端的突变。一些突变即使破坏了最末端的碱基,也没有阻止病毒DNA的整合。其他突变对感染效率有显著影响;在这些情况下,整合前DNA的形成是正常的,但有生产性原病毒的建立受到了阻止。其中一个缺陷突变体产生了一个假回复体,它与野生型不同,但具有正常的感染性。在这种病毒进行的整合反应过程中,病毒DNA有异常数量的碱基被去除。