Frappier D, Gendron D, Bourgaux-Ramoisy D, Bourgaux P
Département de Microbiologie, Faculté de Médecine, Université de Sherbrooke, Québec, Canada.
J Virol. 1990 Oct;64(10):5058-65. doi: 10.1128/JVI.64.10.5058-5065.1990.
RmI, a chimeric DNA molecule containing polyomavirus (Py) and mouse sequences, generates unit-length Py DNA via intramolecular recombination between two directly repeated viral sequences of 182 base pairs (S repeats). To analyze the contribution of the S repeats in this process, we produced mutants of RmI carrying deletions in either one or both S repeats and tested them for their ability to recombine in mouse 3T6 cells. Mutant DNAs were found to yield unit-length Py DNA as long as they carried a minimal internal homology of 40 to 50 base pairs. Unlike RmI itself, however, the mutants also gave rise to nonhomologous recombination products. These results suggest that when the generation of homologous products is hampered by a limiting homology, nonhomologous products may arise instead of homologous ones. Therefore, the initial step(s) in the mechanisms yielding the two kinds of products could be identical.
RmI是一种包含多瘤病毒(Py)和小鼠序列的嵌合DNA分子,它通过两个182个碱基对的直接重复病毒序列(S重复序列)之间的分子内重组产生单位长度的Py DNA。为了分析S重复序列在此过程中的作用,我们构建了在一个或两个S重复序列中携带缺失的RmI突变体,并在小鼠3T6细胞中测试它们的重组能力。发现突变DNA只要携带40至50个碱基对的最小内部同源性就能产生单位长度的Py DNA。然而,与RmI本身不同的是,这些突变体还产生了非同源重组产物。这些结果表明,当同源产物的产生因同源性有限而受阻时,可能会产生非同源产物而非同源产物。因此,产生这两种产物的机制的初始步骤可能是相同的。