Dahlberg A E, Dahlberg J E, Lund E, Tokimatsu H, Rabson A B, Calvert P C, Reynolds F, Zahalak M
Proc Natl Acad Sci U S A. 1978 Aug;75(8):3598-602. doi: 10.1073/pnas.75.8.3598.
We have isolated and partially characterized an endonuclease involved in processing the 5' end of 16S rRNA of Escherichia coli. A mutant strain that is deficient in this enzyme accumulates a new precursor of 16S rRNA, named 16.3S rRNA. This rRNA has the 3' end of mature 16S rRNA but is about 60 nucleotides longer at the 5' end. In vitro, the enzyme preparation cleaves an RNA fragment of about 60 nucleotides from the 5' end of 16.3S rRNA in 30S ribosomal subunits, yielding the mature 5' end of 16S rRNA. In the mutant strain the 16.3S rRNA is associated with a full complement of 21 ribosomal proteins in 30S subunits. These particles, which comprise 50% of the total 30S subunits, are present on polyribosomes.
我们已经分离出一种参与大肠杆菌16S rRNA 5'端加工的核酸内切酶,并对其进行了部分特性分析。缺乏这种酶的突变菌株会积累一种新的16S rRNA前体,命名为16.3S rRNA。这种rRNA具有成熟16S rRNA的3'端,但在5'端大约长60个核苷酸。在体外,该酶制剂从30S核糖体亚基中的16.3S rRNA的5'端切割下一个约60个核苷酸的RNA片段,产生成熟的16S rRNA的5'端。在突变菌株中,16.3S rRNA与30S亚基中的21种核糖体蛋白的完整互补物相关联。这些颗粒占总30S亚基的50%,存在于多核糖体上。