Kravchenko V V, Serpinskiĭ O I, Pletnev A G
Mol Biol (Mosk). 1984 Mar-Apr;18(2):397-403.
The fragment of 124 base pairs (Alu-124) has been isolated from the phage T7 DNA and cloned in the plasmid pSK. The sequence of the fragment was determined and position of this fragment on the physical map of phage DNA was found. It has been found that Alu-124 fragment contained an active in vivo and in vitro promoter for E. coli RNA-polymerase. In vitro transcription from this promoter was initiated with GTP. The start of the transcription was localised at about 104 or 105 nucleotide. The data obtained indicate that the Alu-124 fragment of the phage T7 promoter B, may be involved in the control of the transcription of the phage T7 early stage development.
124个碱基对的片段(Alu - 124)已从噬菌体T7 DNA中分离出来,并克隆到质粒pSK中。测定了该片段的序列,并找到了该片段在噬菌体DNA物理图谱上的位置。已发现Alu - 124片段含有一个对大肠杆菌RNA聚合酶在体内和体外均有活性的启动子。从该启动子进行的体外转录以GTP起始。转录起始位点定位在大约第104或105个核苷酸处。所获得的数据表明,噬菌体T7启动子B的Alu - 124片段可能参与噬菌体T7早期发育转录的调控。