Morosyuk S V, Lee K, SantaLucia J, Cunningham P R
Department of Chemistry Sciences, Wayne State University, Detroit, MI, 48202, USA.
J Mol Biol. 2000 Jun 30;300(1):113-26. doi: 10.1006/jmbi.2000.3852.
Nucleotides 680 to 710 of Escherichia coli 16 S rRNA form a distinct structural domain required for ribosome function. The goal of this study was to determine the functional significance of pairing interactions in the 690 region. Two different secondary structures were proposed for this hairpin, based on phylogenetic and chemical modification studies. To study the effect of pairing interactions in the 690 hairpin on ribosome function and to determine which of the proposed secondary structures is biologically significant, we performed an instant-evolution experiment in which the nine nucleotides that form the proposed base-pairs and dangling ends of the 690 stem were randomly mutated, and functional mutant combinations were selected. A total of 96 unique functional mutants were isolated, assayed in vivo, and sequenced. Analysis of these data revealed extensive base-pairing and stacking interactions among the mutated nucleotides. Formation of either a Watson-Crick base-pair or G.U pair between positions 688 and 699 is absolutely required for ribosome function. We also performed NMR studies of a 31-nucleotide RNA which indicate the formation of a functionally important base-pair between nucleotides 688 and 699. Formation of a second base-pair between positions 689 and 698, however, is not essential for ribosome function, but the level of ribosome function correlates with the predicted thermodynamic stability of the nucleotide pairs in these positions. The universally conserved positions G690 and U697 are generally portrayed as forming a G.U mismatch. Our data show co-variation between these positions, but do not support the hypothesis that the G690:U697 pair forms a wobble structure. NMR studies of model 14-nt and 31-nt RNAs support these findings and show that G690 and U697 are involved in unusual stacking interactions but do not form a wobble pair. Preliminary NMR structural analysis reveals that the loop portion of the 690 hairpin folds into a highly structured and novel conformation.
大肠杆菌16S rRNA的680至710位核苷酸形成核糖体功能所需的一个独特结构域。本研究的目的是确定690区域配对相互作用的功能意义。基于系统发育和化学修饰研究,为这个发夹结构提出了两种不同的二级结构。为了研究690发夹中的配对相互作用对核糖体功能的影响,并确定所提出的二级结构中哪一种具有生物学意义,我们进行了一项即时进化实验,其中形成690茎干中所提出的碱基对和悬垂末端的九个核苷酸被随机突变,并选择了功能性突变组合。总共分离出96个独特的功能性突变体,在体内进行检测并测序。对这些数据的分析揭示了突变核苷酸之间广泛的碱基配对和堆积相互作用。核糖体功能绝对需要在688位和699位之间形成沃森-克里克碱基对或G·U对。我们还对一个31个核苷酸的RNA进行了核磁共振研究,结果表明在688位和699位核苷酸之间形成了一个功能重要的碱基对。然而,在689位和698位之间形成第二个碱基对对于核糖体功能并非必不可少,但核糖体功能水平与这些位置核苷酸对的预测热力学稳定性相关。普遍保守的G690和U697位点通常被描述为形成一个G·U错配。我们的数据显示了这些位点之间的共变,但不支持G690:U697对形成摆动结构的假设。对14核苷酸和31核苷酸模型RNA的核磁共振研究支持了这些发现,并表明G690和U697参与了异常的堆积相互作用,但没有形成摆动对。初步核磁共振结构分析表明,690发夹的环部分折叠成一种高度结构化的新颖构象。