Ryan M J, Belagaje R, Brown E L, Fritz H J, Khorana H G
J Biol Chem. 1979 Nov 10;254(21):10803-10.
The total synthesis of a tyrosine suppressor tRNA gene with a modified promoter is described. The alteration involves the replacement of the four G:C base pairs immediately preceding the start point of transcription by A:T base pairs. The new sequence contains the recognition sequence for the HindIII restriction endonuclease at the transcriptional start point, thus permitting fusion of the structural gene with promoters containing independent sequence modifications. The construction, cloning, and biological activity of several recombinant DNAs containing the tRNA gene with the modified promoter are described. The expression of this gene in vivo is compared with that of both the unmodified synthetic suppressor gene and a naturally occurring tyr su3+ gene cloned onto a multicopy plasmid.
描述了具有修饰启动子的酪氨酸抑制性tRNA基因的全合成。这种改变涉及将转录起始点之前紧邻的四个G:C碱基对替换为A:T碱基对。新序列在转录起始点处包含HindIII限制性内切核酸酶的识别序列,从而允许结构基因与包含独立序列修饰的启动子融合。描述了几种含有修饰启动子的tRNA基因的重组DNA的构建、克隆和生物活性。将该基因在体内的表达与未修饰的合成抑制基因以及克隆到多拷贝质粒上的天然存在的tyr su3+基因的表达进行了比较。