Yoda K, Okazaki T
Department of Molecular Biology, School of Science, Nagoya University, Japan.
Mol Gen Genet. 1991 May;227(1):1-8. doi: 10.1007/BF00260698.
We have surveyed the frequency of each of 64 trinucleotide permutations at every nucleotide frame located from 1 to 15 nucleotides upstream of primer RNA-DNA transition sites mapped within a 1.5 kb region of the bacteriophage lambda genome and a 1.4 kb region of the Escherichia coli genome. We have demonstrated that in both systems initiation of DNA synthesis strongly correlates with a CAG sequence located 11 nucleotides upstream of the DNA start sites. Based on the examination of various reports of the priming reaction catalyzed by E. coli primase in vivo and in vitro, we propose that (i) E. coli primase itself recognizes a 3'GTC 5' sequence on the template strand, (ii) DnaB helicase releases the specificity of E. coli primase and, (iii) the consensus recognition sequence for E. coli primase associated with DnaB helicase is 3'PuPyPy 5'.
我们调查了噬菌体λ基因组1.5 kb区域和大肠杆菌基因组1.4 kb区域内定位的引物RNA - DNA转换位点上游1至15个核苷酸处每个核苷酸框架中64种三核苷酸排列的频率。我们已经证明,在这两个系统中,DNA合成的起始与DNA起始位点上游11个核苷酸处的CAG序列密切相关。基于对大肠杆菌引发酶在体内和体外催化的引发反应的各种报道的研究,我们提出:(i)大肠杆菌引发酶本身识别模板链上的3'GTC 5'序列;(ii)DnaB解旋酶释放大肠杆菌引发酶的特异性;(iii)与DnaB解旋酶相关的大肠杆菌引发酶的共有识别序列是3'PuPyPy 5'。