Johnson R C, Reznikoff W S
Nucleic Acids Res. 1981 Apr 24;9(8):1873-83. doi: 10.1093/nar/9.8.1873.
RNA polymerase is known to undergo a cycling process during initiation of transcription in vitro in which large amounts of small oligonucleotides are released. We have used this cycling reaction to determine the 5' end of the RNA synthesized from the outer ends of the Tn5 inverted repeats. By analyzing the size of the radiolabeled oligonucleotides synthesized using different labeled nucleoside triphosphates and in reactions deficient for a particular nucleoside triphosphate, the partial 5' sequence was obtained. This sequence was correlated with the DNA sequence of the region and an unambiguous origin for the mRNA was determined. The start site for the RNA, which is located at 97 base pairs from the outer ends of the inverted repeats, was confirmed by digesting gamma-32 P-ATP labeled full length (run off) transcripts with ribonuclease T1. The resulting gamma-labeled T1 generated oligonucleotide corresponded to the predicted size determined using the cycling reaction. With the knowledge of the RNA start site, the probable translation start sites for the protein(s) known to be required for Tn5 transposition can be predicted. Possible implications of the DNA sequence with respect to the regulation of the transposase are also discussed.
已知RNA聚合酶在体外转录起始过程中会经历一个循环过程,在此过程中会释放大量的小寡核苷酸。我们利用这个循环反应来确定从Tn5反向重复序列外端合成的RNA的5'端。通过分析使用不同标记的核苷三磷酸合成的放射性标记寡核苷酸的大小,以及在缺乏特定核苷三磷酸的反应中合成的寡核苷酸大小,获得了部分5'序列。将该序列与该区域的DNA序列相关联,确定了mRNA明确的起源。通过用核糖核酸酶T1消化γ-32P-ATP标记的全长(延伸)转录本,证实了位于距反向重复序列外端97个碱基对处的RNA起始位点。产生的γ标记的T1产生的寡核苷酸与使用循环反应确定的预测大小相对应。有了RNA起始位点的信息,就可以预测已知的Tn5转座所需蛋白质的可能翻译起始位点。还讨论了DNA序列对转座酶调控的可能影响。