Christiansen J
Biostructural Chemistry, Kemisk Institut, Aarhus Universitet, Denmark.
Nucleic Acids Res. 1988 Aug 11;16(15):7457-76. doi: 10.1093/nar/16.15.7457.
The secondary structure of the 9S RNA precursor to ribosomal 5S RNA in Escherichia coli has been determined using chemical reagents and ribonucleases in combination with a reverse transcription procedure. The 9S RNA precursor was generated in vitro by T7 RNA polymerase, and the rrnB operon terminator, T1, was able to terminate the in vitro transcript. The secondary structure model exhibits three structural domains corresponding to a 5' region, a mature region and a terminator region. The mature domain is structurally identical to 5S RNA, and the ribosomal proteins L18 and L25 are able to bind to the precursor. The processing endoribonuclease RNase E cleaves between the structural domains. Moreover, an intramolecular refolding of the nascent transcript must take place if the current view of RNase III processing stems is correct.
利用化学试剂、核糖核酸酶并结合逆转录程序,已确定了大肠杆菌核糖体5S RNA的9S RNA前体的二级结构。9S RNA前体由T7 RNA聚合酶在体外生成,rrnB操纵子终止子T1能够终止体外转录物。二级结构模型呈现出对应于5'区域、成熟区域和终止子区域的三个结构域。成熟结构域在结构上与5S RNA相同,核糖体蛋白L18和L25能够与前体结合。加工内切核糖核酸酶RNase E在结构域之间切割。此外,如果目前关于RNase III加工茎的观点正确,新生转录物必须进行分子内重折叠。