King T C, Sirdeshmukh R, Schlessinger D
Proc Natl Acad Sci U S A. 1984 Jan;81(1):185-8. doi: 10.1073/pnas.81.1.185.
RNase III makes the initial cleavages that excise Escherichia coli precursor 16S and 23S rRNA from a single large primary transcript. In mutants deficient in RNase III, no species cleaved by RNase III are detected and the processing of 23S rRNA precursors to form mature 23S rRNA fails entirely. Instead, 50S ribosomes are formed with rRNAs up to several hundred nucleotides longer than mature 23S rRNA. Unexpectedly, these aberrant subunits function well enough to participate in protein synthesis and permit cell growth. Consistent with the inference that RNase III cleavages are absolutely required for 23S rRNA maturation, when 50S ribosomes from a strain deficient in RNase III were incubated with a ribosome-free extract from a RNase III+ strain, rRNA species processed by RNase III and species with normal mature 23S rRNA termini were produced.
核糖核酸酶III进行最初的切割,从单一的大型初级转录本中切除大肠杆菌前体16S和23S核糖体RNA。在核糖核酸酶III缺陷的突变体中,未检测到被核糖核酸酶III切割的物种,并且23S核糖体RNA前体加工形成成熟23S核糖体RNA的过程完全失败。相反,形成的50S核糖体含有比成熟23S核糖体RNA长几百个核苷酸的核糖体RNA。出乎意料的是,这些异常亚基功能良好,足以参与蛋白质合成并允许细胞生长。与核糖核酸酶III切割对于23S核糖体RNA成熟绝对必需的推断一致,当将来自核糖核酸酶III缺陷菌株的50S核糖体与来自核糖核酸酶III+菌株的无核糖体提取物一起孵育时,产生了被核糖核酸酶III加工的核糖体RNA物种和具有正常成熟23S核糖体RNA末端的物种。