Boye E, Skarstad K, Løbner-Olesen A
Department of Cell Biology, Institute for Cancer Research, Montebello, 0310, Oslo, Norway.
Biochim Biophys Acta. 2001 Oct 31;1521(1-3):73-80. doi: 10.1016/s0167-4781(01)00292-5.
Initiation of chromosomal replication in Escherichia coli is dependent on availability of the initiator protein DnaA. We have introduced into E. coli cells plasmids carrying the chromosomal locus datA, which has a high affinity for DnaA. To be able to monitor oriC initiation as a function of datA copy number, we introduced a minichromosome which only replicates from oriC, using a host cell which replicates its chromosome independently of oriC. Our data show that a moderate increase in datA copy number is accompanied by increased DnaA protein synthesis that allows oriC initiation to occur normally, as measured by minichromosome copy number. As datA gene dosage is increased dnaA expression cannot be further derepressed, and the minichromosome copy number is dramatically reduced. Under these conditions the minichromosome was maintained by integration into the chromosome. These findings suggest that the datA locus plays a significant role in regulating oriC initiation, by its capacity to bind DnaA. They also suggest that auto regulation of the dnaA gene is of minor importance in regulation of chromosome initiation.
大肠杆菌中染色体复制的起始依赖于起始蛋白DnaA的可用性。我们已将携带对DnaA具有高亲和力的染色体位点datA的质粒导入大肠杆菌细胞。为了能够监测oriC起始作为datA拷贝数的函数,我们引入了一个仅从oriC复制的微型染色体,使用一个独立于oriC复制其染色体的宿主细胞。我们的数据表明,datA拷贝数适度增加伴随着DnaA蛋白合成增加,这使得oriC起始能够正常发生,如通过微型染色体拷贝数所测量的那样。随着datA基因剂量增加,dnaA表达不能进一步去阻遏,并且微型染色体拷贝数显著降低。在这些条件下,微型染色体通过整合到染色体中得以维持。这些发现表明,datA位点通过其结合DnaA的能力在调节oriC起始中起重要作用。它们还表明,dnaA基因的自动调节在染色体起始调节中不太重要。