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Homologous recombination of monkey alpha-satellite repeats in an in vitro simian virus 40 replication system: possible association of recombination with DNA replication.

机译:在体外猿猴病毒40复制系统中猴α-卫星重复序列的同源重组:重组与DNA复制的可能关联。

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摘要

To study homologous recombination between repeated sequences in an in vitro simian virus 40 (SV40) replication system, we constructed a series of substrate DNAs that contain two identical fragments of monkey alpha-satellite repeats. Together with the SV40-pBR322 composite vector encoding Apr and Kmr, the DNAs also contain the Escherichia coli galactokinase gene (galK) positioned between two alpha-satellite fragments. The alpha-satellite sequence used consists of multiple units of tandem 172-bp sequences which differ by microheterogeneity. The substrate DNAs were incubated in an in vitro SV40 DNA replication system and used to transform the E. coli galK strain DH10B after digestion with DpnI. The number of E. coli galK Apr Kmr colonies which contain recombinant DNAs were determined, and their structures were analyzed. Products of equal and unequal crossovers between identical 172-bp sequences and between similar but not identical (homeologous) 172-bp sequences, respectively, were detected, although those of the equal crossover were predominant among all of the galK mutant recombinants. Similar products were also observed in the in vivo experiments with COS1 cells. The in vitro experiments showed that these recombinations were dependent on the presence of both the SV40 origin of DNA replication and SV40 large T antigen. Most of the recombinant DNAs were generated from newly synthesized DpnI-resistant DNAs. These results suggest that the homologous recombination observed in this SV40 system is associated with DNA replication and is suppressed by mismatches in heteroduplexes formed between similar but not identical sequences.
机译:为了研究体外猿猴病毒40(SV40)复制系统中重复序列之间的同源重组,我们构建了一系列底物DNA,其中包含两个相同的猴α-卫星重复序列片段。这些DNA与编码Apr和Kmr的SV40-pBR322复合载体一起,还包含位于两个α卫星片段之间的大肠杆菌半乳糖激酶基因(galK)。所使用的α-卫星序列由串联的172个bp序列的多个单元组成,这些序列在微异质性方面有所不同。将底物DNA在体外SV40 DNA复制系统中孵育,并在用DpnI消化后用于转化大肠杆菌galK菌株DH10B。确定了含有重组DNA的大肠杆菌galK Apr Kmr菌落的数量,并对其结构进行了分析。尽管在所有galK突变体重组子中,相等交换的占主导地位,但分别检测到相同172bp序列之间以及相似但不相同(同源)的172bp序列之间相等和不相等交换的产物。在COS1细胞的体内实验中也观察到了类似的产物。体外实验表明,这些重组依赖于DNA复制的SV40起源和SV40大T抗原的存在。大部分重组DNA是从新合成的耐DpnI的DNA产生的。这些结果表明,在该SV40系统中观察到的同源重组与DNA复制有关,并被相似但不相同序列之间形成的异源双链体错配抑制。

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