Horvath D, Spiegelman G B
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Nucleic Acids Res. 1988 Mar 25;16(6):2585-99. doi: 10.1093/nar/16.6.2585.
Recombinants between 5' deletion mutants of a tRNA(3bVal) gene which is inactive as an in vitro transcription template and a tRNAArg gene, which is an active in vitro template were made. The 5' flanking region of tRNA(Arg) including 36 nucleotides of the coding sequence of the gene stimulated transcription of the tRNA(3bVal), deleted to the +17 position, gene by over 50 fold. When the 5' flanking region of the tRNA(Arg) gene included 22 nucleotides of the coding sequence stimulation was reduced by a factor of 3. Thus the sequences between +22 and +36 of tRNA(Arg) are required to permit maximum stimulation of tRNA(3bVal) in vitro template activity.
构建了一个无活性的体外转录模板tRNA(3bVal)基因的5'缺失突变体与一个有活性的体外转录模板tRNAArg基因之间的重组体。tRNA(Arg)的5'侧翼区域包括该基因编码序列的36个核苷酸,可使缺失至+17位置的tRNA(3bVal)基因的转录提高50倍以上。当tRNA(Arg)基因的5'侧翼区域包括编码序列的22个核苷酸时,刺激作用降低了3倍。因此,tRNA(Arg)的+22至+36之间的序列是使tRNA(3bVal)体外模板活性获得最大刺激所必需的。