Kordes E, Jock S, Fritsch J, Bosch F, Klug G
Zentrum für Molekulare Biologie Heidelberg, Germany.
J Bacteriol. 1994 Feb;176(4):1121-7. doi: 10.1128/jb.176.4.1121-1127.1994.
In Rhodobacter capsulatus wild-type strains, the 23S rRNA is cleaved into [16S] and [14S] rRNA molecules. Our data show that a region predicted to form a hairpin-loop structure is removed from the 23S rRNA during this processing step. We have analyzed the processing of rRNA in the wild type and in the mutant strain Fm65, which does not cleave the 23S rRNA. In addition to the lack of 23S rRNA processing, strain Fm65 shows impeded processing of a larger 5.6-kb rRNA precursor and slow maturation of 23S and 16S rRNAs from pre-23S and pre-16S rRNA species. Similar effects have also been described previously for Escherichia coli RNase III mutants. Processing of the 5.6-kb precursor was independent of protein synthesis, while the cleavage of 23S rRNA to generate 16S and 14S rRNA required protein synthesis. We identified a DNA fragment of the wild-type R. capsulatus chromosome that conferred normal processing of 5.6-kb rRNA and 23S rRNA when it was expressed in strain Fm65.
在荚膜红细菌野生型菌株中,23S rRNA被切割成[16S]和[14S] rRNA分子。我们的数据表明,在这个加工步骤中,一个预测会形成发夹环结构的区域从23S rRNA中被去除。我们分析了野生型和突变菌株Fm65中rRNA的加工情况,Fm65不会切割23S rRNA。除了缺乏23S rRNA加工外,菌株Fm65还表现出较大的5.6-kb rRNA前体的加工受阻,以及23S和16S rRNA从pre-23S和pre-16S rRNA物种的成熟缓慢。之前也已描述过大肠杆菌RNase III突变体有类似的效应。5.6-kb前体的加工独立于蛋白质合成,而23S rRNA切割产生16S和14S rRNA则需要蛋白质合成。我们鉴定出了野生型荚膜红细菌染色体的一个DNA片段,当它在菌株Fm65中表达时,能赋予5.6-kb rRNA和23S rRNA正常的加工能力。