Gewirth D T, Abo S R, Leontis N B, Moore P B
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06511.
Biochemistry. 1987 Aug 11;26(16):5213-20. doi: 10.1021/bi00390a047.
A method has been found for reassembling fragment 1 of Escherichia coli 5S RNA from mixtures containing strand III (bases 69-87) and the complex consisting of strand II (bases 89-120) and strand IV (bases 1-11). The reassembled molecule is identical with unreconstituted fragment 1. With this technique, fragment 1 molecules have been constructed 15N-labeled either in strand III or in the strand II-strand IV complex. Spectroscopic data obtained with these partially labeled molecules show that the terminal helix of 5S RNA includes the GU and GC base pairs at positions 9 and 10 which the standard model for 5S secondary structure predicts [see Delihas, N., Anderson, J., & Singhal, R. P. (1984) Prog. Nucleic Acid Res. Mol. Biol. 31, 161-190] but that these base pairs are unstable both in the fragment and in native 5S RNA. The data also assign three resonances to the helix V region of the molecule (bases 70-77 and 99-106). None of these resonances has a "normal" chemical shift even though two of them correspond to AU or GU base pairs in the standard model. The implications of these findings for our understanding of the structure of 5S RNA and its complex with ribosomal protein L25 are discussed.
已找到一种方法,可从含有III链(碱基69 - 87)以及由II链(碱基89 - 120)和IV链(碱基1 - 11)组成的复合物的混合物中重新组装大肠杆菌5S RNA的片段1。重新组装的分子与未重构的片段1相同。利用该技术,构建了在III链或II链 - IV链复合物中15N标记的片段1分子。用这些部分标记的分子获得的光谱数据表明,5S RNA的末端螺旋包含5S二级结构标准模型所预测的第9和第10位的GU和GC碱基对[见Delihas, N., Anderson, J., & Singhal, R. P. (1984) Prog. Nucleic Acid Res. Mol. Biol. 31, 161 - 190],但这些碱基对在片段和天然5S RNA中均不稳定。数据还为分子的螺旋V区域(碱基70 - 77和99 - 106)确定了三个共振峰。尽管其中两个共振峰在标准模型中对应于AU或GU碱基对,但这些共振峰均没有“正常”的化学位移。讨论了这些发现对我们理解5S RNA结构及其与核糖体蛋白L25复合物的意义。