Atlung T, Løbner-Olesen A, Hansen F G
Mol Gen Genet. 1987 Jan;206(1):51-9. doi: 10.1007/BF00326535.
Increased synthesis of DnaA protein, obtained with plasmids carrying the dnaA gene controlled by the heat inducible lambda pL promoter, stimulated initiation of replication from oriC about threefold. The overinitiation was determined both as an increase in copy number of a minichromosome and as an increase in chromosomal gene dosage of oriC proximal DNA. The additional replication forks which were initiated on the chromosome did not lead to an overall increase in DNA content. DNA/DNA hybridization showed an amplification encompassing less than a few hundred kilobases on each side of oriC. Kinetic studies showed that the overinitiation occurred very rapidly after the induction, and that the initiation frequency then decreased to a near normal frequency per oriC. The results indicate that the DnaA protein is one important factor in regulation of initiation of DNA replication from oriC.
用携带受热诱导型λ pL启动子控制的dnaA基因的质粒获得的DnaA蛋白合成增加,刺激了从oriC起始的复制约三倍。过量起始既通过微型染色体拷贝数的增加来确定,也通过oriC近端DNA的染色体基因剂量的增加来确定。在染色体上起始的额外复制叉并未导致DNA含量的总体增加。DNA/DNA杂交显示在oriC两侧各有不到几百千碱基的扩增。动力学研究表明,诱导后过量起始非常迅速地发生,然后起始频率降至每个oriC接近正常的频率。结果表明,DnaA蛋白是调控从oriC起始DNA复制的一个重要因素。