Srivastava A K, Schlessinger D
Department of Microbiology and Immunology, Washington University School of Medicine, St Louis, MO 63110.
Nucleic Acids Res. 1989 Feb 25;17(4):1649-63. doi: 10.1093/nar/17.4.1649.
Immediate precursors of 16S rRNA are processed by endonucleolytic cleavage at both 5' and 3' mature termini, with the concomitant release of precursor fragments which are further metabolized by both exo- and endonucleases. In wild-type cells rapid cleavages by RNase III in precursor-specific sequences precede the subsequent formation of the mature ends; mature termini can, however, be formed directly from pre-16S rRNA with no intermediate species. The direct maturation is most evident in a strain deficient in RNase III, and the results in whole cells are consistent with results from maturation reactions in vitro. Thus, maturation does not require cleavages within the double-stranded stems that enclose mature rRNA sequences in the pre-16S rRNA.
16S rRNA的直接前体在5'和3'成熟末端通过内切核酸酶切割进行加工,同时释放出前体片段,这些片段会被外切核酸酶和内切核酸酶进一步代谢。在野生型细胞中,核糖核酸酶III在前体特异性序列中快速切割先于成熟末端的后续形成;然而,成熟末端可以直接从前16S rRNA形成,没有中间物种。这种直接成熟在核糖核酸酶III缺陷的菌株中最为明显,全细胞中的结果与体外成熟反应的结果一致。因此,成熟不需要在包围前16S rRNA中成熟rRNA序列的双链茎内进行切割。