Seery L, Devine K M
Department of Genetics, Trinity College, Dublin, Ireland.
J Bacteriol. 1993 Apr;175(7):1988-94. doi: 10.1128/jb.175.7.1988-1994.1993.
The features which contribute to the activity of the single-stranded origin of the Bacillus plasmid pBAA1 were investigated. This origin is contained on a DNA fragment greater than 116 but less than 191 bases in size. There is the potential to form three stem-loop structures within this fragment. Comparison of the sequence of this origin from pBAA1 with the sequence of a homologous fragment from the Bacillus thuringiensis plasmid pGI2 indicates that both the structure and the relative positioning of the predicted stem-loops are important for origin activity. Deletion analysis suggests that it is the structure of stem-loop III which is important, because it can be replaced by a nonrelated dyad element without significant loss of origin activity. Three sequence motifs are conserved between the origins from pBAA1 and pGI2. Mutation of motif 1 leads to attenuation of single-stranded origin activity. A second motif (motif 3) shares significant homology with a group of single-strand initiation (ssi) sites found on plasmids isolated from Escherichia coli, suggesting that it also contributes to single-stranded origin activity. Our results also indicate that RNA polymerase is utilized to synthesize the RNA primer at the pBAA1 single-stranded origin and that this origin can function in both Bacillus subtilis and Staphylococcus aureus.
对芽孢杆菌质粒pBAA1单链复制起点活性的相关特征进行了研究。该复制起点位于一个大小大于116个碱基但小于191个碱基的DNA片段上。在这个片段内有形成三个茎环结构的潜力。将pBAA1中该复制起点的序列与苏云金芽孢杆菌质粒pGI2的同源片段序列进行比较,结果表明预测的茎环结构及其相对位置对复制起点活性都很重要。缺失分析表明,茎环III的结构很重要,因为它可以被一个不相关的二元元件取代,而不会显著丧失复制起点活性。pBAA1和pGI2的复制起点之间有三个序列基序是保守的。基序1的突变会导致单链复制起点活性减弱。第二个基序(基序3)与从大肠杆菌分离的质粒上发现的一组单链起始(ssi)位点具有显著同源性,这表明它也有助于单链复制起点活性。我们的结果还表明,RNA聚合酶被用于在pBAA1单链复制起点合成RNA引物,并且这个复制起点在枯草芽孢杆菌和金黄色葡萄球菌中都能发挥作用。