Thurlow D L, Ehresmann C, Ehresmann B
Nucleic Acids Res. 1983 Oct 11;11(19):6787-802. doi: 10.1093/nar/11.19.6787.
Nucleotides in 16S rRNA which are required in unmodified form for specific recognition of ribosomal protein S8 from Escherichia coli were identified using a damage-selection experimental approach. Prior to complex formation with S8, 16S rRNA was treated under fully denaturing conditions with either diethyl pyrocarbonate or 25% hydrazine. Following separation of bound from unbound fragments of RNA, those associated with S8 were analyzed for their content of modified bases by treatment with aniline. Nucleotides found to be consistently unmodified in such fragments were located near the base of a stable helix (encompassing bases 581-656) or near the apex of the helix on the 3' proximal side. A minor S8 ribonucleoprotein particle was found to contain fragments which extended in the 3' direction to position 671.
采用损伤选择实验方法,鉴定了16S rRNA中以未修饰形式对来自大肠杆菌的核糖体蛋白S8进行特异性识别所必需的核苷酸。在与S8形成复合物之前,16S rRNA在完全变性条件下用焦碳酸二乙酯或25%肼处理。在将RNA的结合片段与未结合片段分离后,通过用苯胺处理分析与S8相关的片段中修饰碱基的含量。发现在这些片段中始终未修饰的核苷酸位于稳定螺旋(包含碱基581 - 656)的基部附近或3'近端侧螺旋的顶端附近。发现一个较小的S8核糖核蛋白颗粒含有在3'方向延伸至位置671的片段。