Gülland U, Hillen W
Lehrstuhl für Mikrobiologie, Friedrich-Alexander Universität Erlangen-Nürnberg, Germany.
Gene. 1992 May 1;114(1):97-101. doi: 10.1016/0378-1119(92)90713-y.
The 5' ends of the Tn10-encoded mRNAs have been analyzed by quantitative primer extensions of the in vivo synthesized RNA and in vitro run-off transcription. The gene is transcribed by a tandem promoter system consisting of PR1 and PR2. While PR1 contributes about 25% of the total PR activity in vitro, more than 95% of the in vivo-produced transcripts originate from PR2. Transcription from PR2 shows extensive heterogeneity at the 5' ends of the mRNAs in vitro and most likely also in vivo. A deletional and oligodeoxyribonucleotide-directed mutational analysis of the PR2 transcript reveals that length heterogeneity results from reiterative copying of a run of five A's at the transcription start point. In vivo transcription leads to longer reiteration products than in vitro transcription.
通过对体内合成RNA的定量引物延伸和体外 runoff转录,分析了Tn10编码mRNA的5′端。该基因由由PR1和PR2组成的串联启动子系统转录。虽然PR1在体外贡献了约25%的总PR活性,但超过95%的体内产生的转录本源自PR2。PR2转录在体外mRNA的5′端显示出广泛的异质性,在体内很可能也是如此。对PR2转录本的缺失和寡脱氧核糖核苷酸定向突变分析表明,长度异质性是由转录起始点处五个A的重复拷贝引起的。体内转录比体外转录产生更长的重复产物。