Bashkirov V I, Lakomova N M, Prozorov A A
Genetika. 1986 Dec;22(12):2750-7.
The pUB110 and pE194 plasmid cointegrates have been isolated and examined in rec+ and recE4 strains of Bacillus subtilis. Cointegrates were shown to be formed by recombination at the specific site present on both parental plasmids as a short region of homology designated RSA. The RSA consists of 63 nucleotides in pE194 and 49 in pUB110; the length of its fully conserved core segment is 10 nucleotides. All cointegrates examined were formed by single crossover event taking place within the core segment, and as a result they have identical nucleotide sequences of recombination junctions. No conversion of mismatched base pairs to nucleotide sequences originally belonging to one of the parental plasmids was found. Though the action of RecE gene did not affect the frequency of cointegrate formation, it was reduced in rec149 host by one order of magnitude. Cointegrates retained their stability during transformation.
已分离出pUB110和pE194质粒共整合体,并在枯草芽孢杆菌的rec⁺和recE4菌株中进行了检测。共整合体显示是通过两个亲本质粒上存在的特定位点处的重组形成的,该特定位点是一个称为RSA的短同源区域。RSA在pE194中由63个核苷酸组成,在pUB110中由49个核苷酸组成;其完全保守的核心片段长度为10个核苷酸。所有检测的共整合体都是由发生在核心片段内的单交换事件形成的,因此它们具有相同的重组连接点核苷酸序列。未发现错配碱基对转换为原本属于亲本质粒之一的核苷酸序列的情况。虽然RecE基因的作用不影响共整合体形成的频率,但在rec149宿主中其形成频率降低了一个数量级。共整合体在转化过程中保持其稳定性。