Smorawinska M, Kuramitsu H K
Department of Oral Biology, State University of New York, Buffalo 14214-3092, USA.
Oral Microbiol Immunol. 1995 Jun;10(3):188-92. doi: 10.1111/j.1399-302x.1995.tb00141.x.
To characterize the promoter structures of Streptococcus mutans genes, primer extension analysis was carried out with 4 genes previously isolated in this laboratory. An analysis of the transcription start sites for the gtfB, gtfC, gtfD and ftf genes revealed that each transcript was initiated at a purine residue. Based on these sites, the -10 and -35 sequences for each transcript were deduced and compared. For all 4 transcripts, the -10, but not the -35, sequences were homologous to the Escherichia coli promoter consensus sequences.
为了表征变形链球菌基因的启动子结构,我们用本实验室之前分离出的4个基因进行了引物延伸分析。对gtfB、gtfC、gtfD和ftf基因的转录起始位点分析表明,每个转录本均起始于一个嘌呤残基。基于这些位点,推导并比较了每个转录本的-10和-35序列。对于所有4个转录本,-10序列而非-35序列与大肠杆菌启动子共有序列同源。