Prescott C D, Kleuvers B, Göringer H U
MAX-Planck-Institut für Molekulare Genetik, Abt Wittmann, Berlin, Germany.
Biochimie. 1991 Jul-Aug;73(7-8):1121-9. doi: 10.1016/0300-9084(91)90155-t.
A series of site-directed mutations has been constructed in E coli 16S rRNA and shown to suppress UGA-dependent translational termination. With the exception of the C726 to G base change, all were constructed in helix 34. Characterization of these mutations is reviewed here and from these data and mRNA-rRNA base pairing model for the termination event is presented. The interaction functions via antiparallel base pairing between either 1 of the 2 UCA motifs in helix 34 and the complementary UGA stop codon on the message, thus forming a quasicontinuous A-type helical structure that is further stabilized by stacking enthalpy. Finally, rRNA motifs potentially required for UAA and UAG-dependent translational termination are discussed.
在大肠杆菌16S rRNA中构建了一系列定点突变,并显示其可抑制UGA依赖的翻译终止。除了C726到G的碱基变化外,所有突变均构建在螺旋34中。本文回顾了这些突变的特征,并根据这些数据提出了终止事件的mRNA-rRNA碱基配对模型。该相互作用通过螺旋34中两个UCA基序之一与信息上互补的UGA终止密码子之间的反平行碱基配对起作用,从而形成准连续的A型螺旋结构,该结构通过堆积焓进一步稳定。最后,讨论了UAA和UAG依赖的翻译终止可能需要的rRNA基序。