Disqué-Kochem C, Seidel U, Helsberg M, Eichenlaub R
Mol Gen Genet. 1986 Jan;202(1):132-5. doi: 10.1007/BF00330529.
At the XhoI site (45.08F) of plasmid mini-F a deletion of 649 bp was generated employing exonuclease Bal31. By this deletion nucleotide sequences functioning as origin II and the four 19 bp direct repeats constituting the incB region in front of the E protein gene were removed from the plasmid. Analysis of proteins radioactively labelled in Escherichia coli mini-cells indicated that all mini-F encoded proteins are expressed. However, the plasmid carrying the deletion was not capable of replicating from the primary origin (origin I, 42.6F). Recently a smaller deletion at the XhoI site (45.08F) of about 300 bp, removing only the region functioning as origin II and replicating from origin I, was described by Tanimoto and Iino (1984, 1985). The data presented suggest that the incB repeats are essential for the initiation of replication from origin I, and possibly also from origin II, and seem not to be engaged in the autoregulation of E protein expression.
在质粒mini-F的XhoI位点(45.08F),利用核酸外切酶Bal31产生了一个649 bp的缺失。通过该缺失,作为II型复制起点的核苷酸序列以及构成E蛋白基因前incB区域的四个19 bp同向重复序列从质粒中被去除。在大肠杆菌微型细胞中对放射性标记蛋白的分析表明,所有mini-F编码的蛋白都能表达。然而,携带该缺失的质粒无法从主要复制起点(I型复制起点,42.6F)进行复制。最近,Tanimoto和Iino(1984年、1985年)描述了在XhoI位点(45.08F)有一个约300 bp的较小缺失,该缺失仅去除了作为II型复制起点的区域,并能从I型复制起点进行复制。所呈现的数据表明,incB重复序列对于从I型复制起点起始复制是必不可少的,可能对从II型复制起点起始复制也是必不可少的,而且似乎不参与E蛋白表达的自动调节。