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Probing the secondary structure of expansion segment ES6 in 18S ribosomal RNA

机译:探索18S核糖体RNA中扩展段ES6的二级结构

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Expansion segment ES6 in 18S ribosomal RNA is, unlike many other expansion segments, present in all eukaryotes. The available data suggest that ES6 is located on the surface of the small ribosomal subunit. Here we have analyzed the secondary structure of the complete ES6 sequence in intact ribosomes from three eukaryotes, wheat, yeast, and mouse, representing different eukaryotic kingdoms. The availability of the ES6 sequence for modification and cleavage by structure sensitive chemicals and enzymatic reagents was analyzed by primer extension and gel electrophoresis on an ABI 377 automated DNA sequencer. The experimental results were used to restrict the number of possible secondary structure models of ES6 generated by the folding software MFOLD. The modification data obtained from the three experimental organisms were very similar despite the sequence variation. Consequently, similar secondary structure models were obtained for the ES6 sequence in wheat, yeast, and mouse ribosomes. A comparison of sequence data from more than 6000 eukaryotes showed that similar structural elements could also be formed in other organisms. The comparative analysis also showed that the extent of compensatory base changes in the suggested helices was low. The in situ structure analysis was complemented by a secondary structure analysis of wheat ES6 transcribed and folded in vitro. The obtained modification data indicate that the secondary structure of the in vitro transcribed sequence differs from that observed in the intact ribosome. These results suggest that chaperones, ribosomal proteins, and/or tertiary rRNA interactions could be involved in the in vivo folding of ES6.
机译:与许多其他扩展段不同,所有真核生物均存在18S核糖体RNA中的扩展段ES6。现有数据表明ES6位于小核糖体亚基的表面。在这里,我们分析了来自三个真核生物(小麦,酵母和小鼠)的完整核糖体中完整ES6序列的二级结构,它们代表了不同的真核生物王国。通过在ABI 377自动DNA测序仪上进行引物延伸和凝胶电泳,分析了结构敏感的化学物质和酶试剂对ES6序列进行修饰和切割的可用性。实验结果用于限制折叠软件MFOLD生成的ES6可能的二级结构模型的数量。尽管序列变化,但从三种实验生物获得的修饰数据非常相似。因此,在小麦,酵母和小鼠核糖体中获得了类似的ES6序列二级结构模型。对来自6000多个真核生物的序列数据进行的比较表明,在其他生物中也可能形成相似的结构元件。比较分析还显示,建议的螺旋中补偿性碱基变化的程度较低。原位结构分析得到了在体外转录和折叠的小麦ES6二级结构的补充。获得的修饰数据表明,体外转录序列的二级结构不同于完整核糖体中观察到的二级结构。这些结果表明,伴侣,核糖体蛋白和/或第三级rRNA相互作用可能与ES6的体内折叠有关。

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