Hogan A, Faust E A
Mol Cell Biol. 1986 Aug;6(8):3005-9. doi: 10.1128/mcb.6.8.3005-3009.1986.
The mechanism of nonhomologous recombination in murine cells infected with the parvovirus minute virus of mice (MVM) has been investigated by analysis of DNA sequences at recombination junctions in naturally occurring deletion variants of the virus. We report here that nonhomologous recombination in the MVM chromosome is characterized by short homologies, by insertion at recombination junctions of foreign DNA sequences that are enriched for preferred eucaryotic topoisomerase I cleavage sites, and by an association with a common DNA sequence motif of the type 5'-CTATTTCT-3'. Additional analyses of broken MVM chromosomes provided evidence for specific enzymatic cleavage within 5'-CTTATC-3' and 5'-CTATTC-3' sequences. The results indicate that the 5'-CTATTTCT-3' motif is an important genetic element for nonhomologous recombination in the parvovirus chromosome.
通过分析小鼠细小病毒(MVM)天然缺失变异体中重组连接点处的DNA序列,对感染该细小病毒的鼠细胞中非同源重组的机制进行了研究。我们在此报告,MVM染色体中的非同源重组具有以下特征:存在短同源性,在重组连接点处插入富含真核生物拓扑异构酶I优先切割位点的外源DNA序列,并且与5'-CTATTTCT-3'类型的常见DNA序列基序相关。对断裂的MVM染色体的进一步分析为5'-CTTATC-3'和5'-CTATTC-3'序列内的特异性酶切提供了证据。结果表明,5'-CTATTTCT-3'基序是细小病毒染色体中非同源重组的重要遗传元件。