Sirdeshmukh R, Schlessinger D
Nucleic Acids Res. 1985 Jul 25;13(14):5041-54. doi: 10.1093/nar/13.14.5041.
In an RNase III-deficient strain of E. coli 23S pre-rRNA accumulates unprocessed in 50S ribosomes and in polysomes. These ribosomes provide a substrate for the analysis of rRNA maturation in vitro. S1 nuclease protection analysis of the products obtained in in vitro processing reactions demonstrates that 23S rRNA processing is ordered. The double stranded stem of 23S rRNA is cleaved by RNase III in vitro to two intermediate RNAs at the 5' end and one at the 3' end. Mature termini are then produced by other enzyme(s) in a soluble protein fraction from wild-type cells. The nature of the reaction at the 5' end is not clear, but the reaction at the 3' end is exonucleolytic, producing three heterogeneous mature termini. The two reactions are coordinated; 3' end maturation progresses concurrently with cleavages at the 5' end. Two results suggest a possible link between final maturation and translation: in vitro, mature termini are formed efficiently in the presence of additives required for protein synthesis; and all the processing intermediates detected from in vitro reactions are also found in polysomes from wild-type cells.
在大肠杆菌的核糖核酸酶III缺陷菌株中,23S前体核糖体RNA(pre-rRNA)在50S核糖体和多核糖体中积累且未被加工。这些核糖体为体外rRNA成熟分析提供了底物。对体外加工反应所得产物进行S1核酸酶保护分析表明,23S rRNA的加工是有序的。23S rRNA的双链茎在体外被核糖核酸酶III切割成5'端的两个中间RNA和3'端的一个中间RNA。然后,野生型细胞可溶性蛋白组分中的其他酶产生成熟末端。5'端反应的性质尚不清楚,但3'端反应是核酸外切反应,产生三个异质的成熟末端。这两个反应是协同的;3'端成熟与5'端切割同时进行。两个结果表明最终成熟与翻译之间可能存在联系:在体外,在蛋白质合成所需添加剂存在的情况下可有效形成成熟末端;并且从体外反应中检测到的所有加工中间体也存在于野生型细胞的多核糖体中。