Lo A C, Liu W Y, Culham D E, Nazar R N
Department of Molecular Biology and Genetics, University of Guelph, Ont., Canada.
Biochem Cell Biol. 1987 Jun;65(6):536-42. doi: 10.1139/o87-069.
Diethyl pyrocarbonate reactivity and thermal denaturation were used to probe potential ribosomal interactions between tRNA and the small 5.8S and 5S rRNAs. Puromycin, an analogue of the terminal aminoacyl-adenosine portion of aminoacyl-tRNA, was observed to increase the accessibility of the 5.8S rRNA, including the highly conserved GAACp sequences. EDTA which releases both tRNA and the 5S rRNA-protein complex resulted in an even greater accessibility in the 5.8S rRNA. The thermal dissociation of whole ribosomes resulted in the release of all three RNAs, with a striking similarity in the denaturation profiles. These results strongly suggest an interdependence in the ribosome-associated structures of the small rRNAs and provide in situ evidence for the various 5S rRNA, 5.8S rRNA, and tRNA containing ribonucleoprotein complexes previously reconstituted through affinity chromatography.
焦碳酸二乙酯反应性和热变性被用于探究tRNA与小的5.8S和5S rRNA之间潜在的核糖体相互作用。嘌呤霉素是氨酰-tRNA末端氨酰腺苷部分的类似物,据观察它会增加5.8S rRNA的可及性,包括高度保守的GAACp序列。能释放tRNA和5S rRNA-蛋白质复合物的EDTA导致5.8S rRNA有更高的可及性。完整核糖体的热解离导致所有三种RNA的释放,其变性图谱有显著相似性。这些结果有力地表明小rRNA的核糖体相关结构之间存在相互依赖性,并为先前通过亲和层析重组的各种含5S rRNA、5.8S rRNA和tRNA的核糖核蛋白复合物提供了原位证据。