Juzumiene D I, Wollenzien P
Department of Biochemistry, North Carolina State University, Raleigh 27695-7622, USA.
RNA. 2000 Jan;6(1):26-40. doi: 10.1017/s1355838200991659.
The organization of the 5' terminus region in the 16S rRNA was investigated using a series of RNA constructs in which the 5' terminus was extended by 5 nt or was shortened to give RNA molecules that started at positions -5, +1, +5, +8, +14, or +21. The structural and functional effects of the 5' extension/truncations were determined after the RNAs were reconstituted. 30S subunits containing 16S rRNA with 5' termini at -5, +1, +5, +8 and +14 had similar structures (judged by UV-induced crosslinking) and exhibited a gradual reduction in tRNA binding activity compared to that seen with 30S subunits reconstituted with native 16S rRNA. To create the 5' terminal site-specific photocrosslinking agent, the reagent azidophenacylbromide (APAB) was attached to the 5' terminus of 16S rRNA through a guanosine monophosphorothioate and the APA-16S rRNAs were reconstituted. Crosslinking carried out with the APA revealed sites in six regions around positions 300-340, 560, 900, 1080, the 16S rRNA decoding region, and at 1330. Differences in the pattern and efficiency of crosslinking for the different constructs allow distance estimates for the crosslinked sites from nucleotide G9. These measurements provide constraints for the arrangement of the RNA elements in the 30S subunit. Similar experiments carried out in the 70S ribosome resulted in a five- to tenfold lower frequency of crosslinking. This is most likely due to a repositioning of the 5' terminus upon subunit association.
使用一系列RNA构建体研究了16S rRNA中5'末端区域的组织方式,其中5'末端延伸了5个核苷酸,或被缩短以产生从-5、+1、+5、+8、+14或+21位置起始的RNA分子。在RNA重构后确定了5'延伸/截短的结构和功能效应。含有5'末端位于-5、+1、+5、+8和+14的16S rRNA的30S亚基具有相似的结构(通过紫外线诱导的交联判断),与用天然16S rRNA重构的30S亚基相比,其tRNA结合活性逐渐降低。为了创建5'末端位点特异性光交联剂,试剂叠氮苯甲酰溴(APAB)通过鸟苷单硫代磷酸酯连接到16S rRNA的5'末端,并对APA-16S rRNAs进行了重构。用APA进行的交联揭示了16S rRNA中300 - 340、560、900、1080、解码区域以及1330位置周围六个区域的位点。不同构建体的交联模式和效率差异允许估计交联位点与核苷酸G9之间的距离。这些测量为30S亚基中RNA元件的排列提供了限制。在70S核糖体中进行的类似实验导致交联频率降低了五到十倍。这很可能是由于亚基缔合后5'末端的重新定位。