Hogan J J, Gutell R R, Noller H F
Biochemistry. 1984 Jul 3;23(14):3322-30. doi: 10.1021/bi00309a032.
Yeast 40S ribosomal subunits have been reacted with kethoxal to probe the conformation of 18S rRNA. Over 130 oligonucleotides were isolated by diagonal electrophoresis and sequenced, allowing identification of 48 kethoxal-reactive sites in the 18S rRNA chain. These results generally support a secondary structure model for 18S rRNA derived from comparative sequence analysis. Significant reactivity at positions 1436 and 1439, in a region shown to be base paired by comparative analysis, lends support to the earlier suggestion [Chapman, N.M., & Noller, H.F. (1977) J. Mol. Biol 109, 131-149] that part of the 3'-major domain of 16S-like rRNAs may undergo a biologically significant conformational rearrangement. Modification of positions in 18S rRNA analogous to those previously found for Escherichia coli 16S rRNA argues for extensive structural homology between 30S and 40S ribosomal subunits, particularly in regions thought to be directly involved in translation.
酵母40S核糖体亚基已与乙二醛反应,以探测18S rRNA的构象。通过对角线电泳分离并测序了130多个寡核苷酸,从而确定了18S rRNA链中的48个乙二醛反应位点。这些结果总体上支持了通过比较序列分析得出的18S rRNA二级结构模型。在通过比较分析显示为碱基配对的区域中,1436位和1439位有显著反应性,这支持了早期的观点[查普曼,N.M.,&诺勒,H.F.(1977年)《分子生物学杂志》109,131 - 149],即16S样rRNA的3'-主要结构域的一部分可能会发生具有生物学意义的构象重排。18S rRNA中与先前在大肠杆菌16S rRNA中发现的类似位置的修饰表明,30S和40S核糖体亚基之间存在广泛的结构同源性,特别是在被认为直接参与翻译的区域。