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Modification of human beta-globin locus PAC clones by homologous recombination in Escherichia coli.

机译:通过在大肠杆菌中的同源重组修饰人β-珠蛋白基因座PAC克隆。

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We report here modifications of human beta-globin PAC clones by homologous recombination in Escherichia coli DH10B, utilising a plasmid temperature sensitive for replication, the recA gene and a wild-type copy of the rpsL gene which allows for an efficient selection for plasmid loss in this host. High frequencies of recombination are observed even with very small lengths of homology and the method has general utility for introducing insertions, deletions and point mutations. No rearrangements were detected with the exception of one highly repetitive genomic sequence when either the E.COLI: RecA- or the lambdoid phage encoded RecT and RecE-dependent recombination systems were used.
机译:我们在这里报告人β-珠蛋白PAC克隆的修饰,通过在大肠杆菌DH10B中进行同源重组,利用对复制敏感的质粒温度,recA基因和rpsL基因的野生型拷贝,从而可以有效选择质粒在这个主人。即使具有非常短的同源性,也观察到了高频率的重组,并且该方法对于引入插入,缺失和点突变具有普遍的实用性。当使用E.COLI:RecA-或lambdoid噬菌体编码的RecT和RecE依赖性重组系统时,除了一个高度重复的基因组序列外,未检测到重排。

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