Proctor David J, Schaak Janell E, Bevilacqua Joanne M, Falzone Christopher J, Bevilacqua Philip C
Department of Chemistry, The Pennsylvania State University, University Park, PA 16802, USA.
Biochemistry. 2002 Oct 8;41(40):12062-75. doi: 10.1021/bi026201s.
RNA is known to fold into a variety of structural elements, many of which have sufficient sequence complexity to make the thermodynamic study of each possible variant impractical. We previously reported a method for isolating stable and unstable RNA sequences from combinatorial libraries using temperature gradient gel electrophoresis (TGGE). This method was used herein to analyze a six-nucleotide RNA hairpin loop library. Three rounds of in vitro selection were performed using TGGE, and unusually stable RNAs were identified by cloning and sequencing. Known stable tetraloops were found, including sequences belonging to the UNCG motif closed by a CG base pair, and the CUUG motif closed by a GC base pair. In addition, unknown tetraloops were found that were nearly as stable as cUNCGg, including sequences related through substitution of the U with a C (Y), the C with an A (M), or both. These substitutions allow hydrogen bonding and stacking interactions in the UNCG loop to be maintained. Thermodynamic analysis of YNMG and variant loops confirmed optimal stability with Y at position 1 and M at position 3. Similarity in structure and stability among YNMG loops was further supported by deoxyribose substitution, CD, and NMR experiments. A conserved tertiary interaction in 16S rRNA exists between a YAMG loop at position 343 and two adenines in the loop at position 159 (Escherichia coli numbering). NMR and functional group substitution experiments suggest that YNAG loops in particular have enhanced flexibility, which allows the tertiary interaction to be maintained with diverse loop sequences at position 159. Taken together, these results support the existence of an extended family of UNCG-like tetraloops with the motif cYNMGg that are thermodynamically stable and structurally similar and can engage in tertiary interactions in large RNA molecules.
已知RNA可折叠成多种结构元件,其中许多元件具有足够的序列复杂性,使得对每个可能变体进行热力学研究不切实际。我们之前报道了一种使用温度梯度凝胶电泳(TGGE)从组合文库中分离稳定和不稳定RNA序列的方法。本文使用该方法分析了一个六核苷酸RNA发夹环文库。使用TGGE进行了三轮体外筛选,并通过克隆和测序鉴定了异常稳定的RNA。发现了已知的稳定四环,包括属于由CG碱基对封闭的UNCG基序的序列,以及由GC碱基对封闭的CUUG基序的序列。此外,还发现了与cUNCGg几乎一样稳定的未知四环,包括通过将U替换为C(Y)、将C替换为A(M)或两者同时替换而相关的序列。这些替换使得UNCG环中的氢键和堆积相互作用得以维持。对YNMG和变体环的热力学分析证实,在位置1为Y且位置3为M时具有最佳稳定性。脱氧核糖取代、圆二色光谱(CD)和核磁共振(NMR)实验进一步支持了YNMG环在结构和稳定性上的相似性。在16S rRNA中,位置343处的YAMG环与位置159处环中的两个腺嘌呤之间存在保守的三级相互作用(大肠杆菌编号)。NMR和官能团取代实验表明,特别是YNAG环具有增强的灵活性,这使得在位置159处能够与不同的环序列维持三级相互作用。综上所述,这些结果支持存在一个扩展的类UNCG四环家族,其基序为cYNMGg,它们在热力学上稳定且结构相似,并且能够在大型RNA分子中参与三级相互作用。