首页> 外文期刊>Nucleic acids research >Site-directed cross-linking of mRNA analogues to 16S ribosomal RNA; a complete scan of cross-links from all positions between ‘+ 1' and ‘+ 16' on the mRNA, downstream from the decoding site
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Site-directed cross-linking of mRNA analogues to 16S ribosomal RNA; a complete scan of cross-links from all positions between ‘+ 1' and ‘+ 16' on the mRNA, downstream from the decoding site

机译:mRNA类似物与16S核糖体RNA的定点交联;在解码位点下游,对mRNA上“ +1”和“ +16”之间所有位置的交叉链接进行完整扫描

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mRNA analogues containing 4-thiouridine residues at selected sites were used to extend our analysis of photo-Induced cross-links between mRNA and 16S RNA to cover the entire downstream range between positions +1 and +16 on the mRNA (position +1 Is the 5′-base of the P-site codon). No tRNA-dependent cross-links were observed from positions +1, + 2, +3 or + 5. Position + 4 on the mRNA was cross-linked In a tRNA-dependent manner to 16S RNA at a site between nucleotides ca 1402–1415 (most probably to the modified residue 1402), and this was absolutely specific for the + 4 position. Similarly, the previously observed cross-link to nucleotide 1052 was absolutely specific for the + 6 position. The previously observed cross-links from + 7 to nucleotide 1395 and from + 11 to 532 were however seen to a lesser extent with certain types of mRNA sequence from neighbouring positions (+ 6 to +10, and +10 to +13, respectively); no tRNA-dependent cross-links to other sites on 16S RNA were found from these positions, and no cross-linking was seen from positions + 14 to + 16. In each case the effect of a second cognate tRNA (at the ribosomal A-site) on the level of cross-linking was studied, and the specificity of each cross-link was confirmed by translocation experiments with elongation factor G, using appropriate mRNA analogues.
机译:在选定位点包含4-硫尿苷残基的mRNA类似物用于扩展我们对mRNA和16S RNA之间的光诱导交联的分析,以覆盖mRNA上+1和+16位之间的整个下游范围(位置+1是P位密码子的5'-碱基)。在+1,+,+ 2,+ 3或+ 5位置未观察到tRNA依赖的交联。mRNA的+4位以tRNA依赖的方式在核苷酸ca 1402–2之间的位点与16S RNA交联。 1415(最可能是修饰残基1402),这绝对是+4位的。类似地,先前观察到的与核苷酸1052的交联对于+6位是绝对特异性的。然而,先前观察到的从+ 7到核苷酸1395的交联和从+ 11到532的交联在邻近位置的某些类型的mRNA序列中的程度较小(分别为+ 6至+10和+10至+13)。 ;从这些位置未发现与16S RNA上其他位点的tRNA依赖性交联,并且从+14至+ 16位未发现交联。在每种情况下,第二个同源tRNA的作用(在核糖体A-研究了在交联水平上的位点),并使用适当的mRNA类似物通过与延伸因子G进行的易位实验证实了每个交联的特异性。

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