Ringuette M, Spencer J H
J Virol. 1987 Jul;61(7):2297-303. doi: 10.1128/JVI.61.7.2297-2303.1987.
Protection of restriction endonuclease cleavage sites by Escherichia coli RNA polymerase bound to the replicative form I of bacteriophage S13 DNA has been used to identify a number of regions of RNA polymerase binding. Digestion with HincII, AluI, HinfI, or HaeIII, under conditions optimized for "open" complex formation, revealed 12 regions of RNA polymerase binding. Based on differential salt sensitivities, five of the regions were classified as strong or tight binding sites. These were located before genes A (two sites), B, and D and at the 5' end of gene F. The seven regions which exhibited weaker binding were located at the 5' end of gene C (two sites), in the middle of gene D, just before and at the 3' end of gene F, at the 5' end of gene G, and in the middle of gene H. The sites before genes B and D coincide with sites previously identified as promoters in bacteriophage phi X174. One of the sites before gene A, that at nucleotides 5175-5211, represents a new putative promoter site in bacteriophage S13 and phi X174 located before the previously identified A gene promoter at nucleotides 10-45.
利用与噬菌体S13 DNA复制型I结合的大肠杆菌RNA聚合酶对限制性内切核酸酶切割位点的保护作用,已鉴定出多个RNA聚合酶结合区域。在针对“开放”复合物形成优化的条件下,用HincII、AluI、HinfI或HaeIII进行消化,揭示了12个RNA聚合酶结合区域。根据不同的盐敏感性,其中5个区域被归类为强结合或紧密结合位点。它们位于基因A之前(两个位点)、基因B、基因D之前以及基因F的5'端。表现出较弱结合的7个区域位于基因C的5'端(两个位点)、基因D的中间、基因F之前及3'端、基因G的5'端以及基因H的中间。基因B和基因D之前的位点与先前在噬菌体phi X174中鉴定为启动子的位点一致。基因A之前的一个位点,即核苷酸5175 - 5211处的位点,代表噬菌体S13和phi X174中一个新的假定启动子位点,位于先前鉴定的位于核苷酸10 - 45处的A基因启动子之前。