Kuchino Y, Mori F, Nishimura S
Nucleic Acids Res. 1985 May 10;13(9):3213-20. doi: 10.1093/nar/13.9.3213.
A 5 kbp DNA fragment containing the tRNAPro1 gene from Escherichia coli was cloned into Charon 21A phage and sequenced by the M13 DNA sequencing technique. When the cloned DNA fragment was used as a template for in vitro transcription with E. coli RNA polymerase, a tRNAPro1 precursor of 120 nucleotide residues was obtained. The tRNAPro1 gene transcribed as a single transcription unit was followed by two unusual repeating sequences, both of 108 bp. These two repeating sequences were separated by a 60 bp spacer sequence. The 5'-portion of each repeating sequence overlapped 19 bp of the 3'-terminal region of the tRNAPro1 gene just like the repeating sequences in the E. coli tRNATyr1 gene. A rho-independent termination was present in the first repeating unit.
将一段包含来自大肠杆菌的tRNAPro1基因的5千碱基对DNA片段克隆到Charon 21A噬菌体中,并采用M13 DNA测序技术进行测序。当将克隆的DNA片段用作大肠杆菌RNA聚合酶体外转录的模板时,获得了一个由120个核苷酸残基组成的tRNAPro1前体。作为单个转录单元转录的tRNAPro1基因后面跟着两个不寻常的重复序列,均为108碱基对。这两个重复序列由一个60碱基对的间隔序列隔开。每个重复序列的5'部分与tRNAPro1基因3'末端区域的19个碱基对重叠,就像大肠杆菌tRNATyr1基因中的重复序列一样。在第一个重复单元中存在一个不依赖ρ因子的终止子。