Persson C, Nordström K
Mol Gen Genet. 1986 Apr;203(1):189-92. doi: 10.1007/BF00330402.
A 500 bp DNA fragment located in the vicinity of the origin of replication of plasmid RSF1010 was cloned into the plasmid vector pBR322 and shown to exhibit incompatibility against parental RSF1010. The rightmost region of this fragment contains three perfect 20 bp direct repeats and a fourth half-repeat of 11 bp, as shown by DNA sequencing. Deletion of the four repeats from the cloned fragment resulted in complete loss of incompatibility whereas partial deletion of the repeated sequence resulted in a concurrent decrease in the expression of incompatibility. We conclude that the incompatibility determinant of RSF1010 is defined by the four repeats and also that the incompatibility expressed is not very strong, since the presence of about 1.5 times as many copies of the repeated sequence as are normally in a cell does not cause a total switch off of RSF1010 replication, but only a 40% reduction in the rate of replication.
将位于质粒RSF1010复制起点附近的一段500 bp DNA片段克隆到质粒载体pBR322中,并显示出与亲本RSF1010不相容。DNA测序表明,该片段的最右侧区域包含三个完美的20 bp直接重复序列和一个11 bp的第四个半重复序列。从克隆片段中删除这四个重复序列导致不相容性完全丧失,而重复序列的部分缺失导致不相容性表达同时降低。我们得出结论,RSF1010的不相容性决定因素由这四个重复序列定义,并且所表达的不相容性不是很强,因为重复序列的拷贝数约为细胞中正常拷贝数的1.5倍时,不会导致RSF1010复制完全关闭,而只会使复制速率降低40%。