Zhu J, Wartell R M
School of Biology, Georgia Institute of Technology, Atlanta, Georgia 30332, USA.
Biochemistry. 1999 Nov 30;38(48):15986-93. doi: 10.1021/bi9916372.
Forty-eight RNA duplexes were constructed that contained all common single base bulges at six different locations. The stabilities of the RNAs were determined by temperature gradient gel electrophoresis (TGGE). The relative stability of a single base bulge was dependent on both base identity and the nearest neighbor context. The single base bulges were placed into two categories. A bulged base with no identical neighboring base was defined as a Group I base bulge. Group II-bulged bases had at least one neighboring base identical to it. Group II bulges were generally more stable than Group I bulges in the same nearest neighbor environments. This indicates that position degeneracy of an unpaired base enhances stability. Differences in the mobility transition temperatures between the RNA fragments with bulges and the completely base-paired reference RNAs were related to free energy differences. Simple models for estimating the free energy contribution of single base bulges were evaluated from the free energy difference data. The contribution of a Group I bulge 5'-(XNZ)-3'.5'-(Z'-X')-3' where N is the unpaired base and X.X' and Z.Z' the neighboring base pairs, could be well-represented (+/-0.34 kcal/mol) by the equation, DeltaG((X)(N)()(Z))(.)((Z)(')(-)(X)(')()) = 3.11 + 0. 40DeltaG(s)()((XZ))(.)((Z)(')(X)(')()). DeltaG(s)()((XZ))(. )((Z)(')(X)(')()) is the stacking energy of the closing base pair doublet. By adding a constant term, delta = -0.3 kcal/mol, to the right side of the above equation, free energies of Group II bulges could also be predicted with the same accuracy. The term delta represents the stabilizing effect due to position degeneracy. A similar equation/model was applied to previous data from 32 DNA fragments with single base bulges. It predicted the free energy differences with a similar standard deviation.
构建了48个RNA双链体,它们在六个不同位置包含所有常见的单碱基凸起。通过温度梯度凝胶电泳(TGGE)测定RNA的稳定性。单碱基凸起的相对稳定性取决于碱基身份和最近邻序列。单碱基凸起分为两类。没有相同相邻碱基的凸起碱基被定义为I组碱基凸起。II组凸起碱基至少有一个与其相同的相邻碱基。在相同的最近邻环境中,II组凸起通常比I组凸起更稳定。这表明未配对碱基的位置简并性增强了稳定性。有凸起的RNA片段与完全碱基配对的参考RNA之间的迁移转变温度差异与自由能差异有关。根据自由能差异数据评估了用于估计单碱基凸起自由能贡献的简单模型。I组凸起5'-(XNZ)-3'.5'-(Z'-X')-3'(其中N是未配对碱基,X、X'和Z、Z'是相邻碱基对)的贡献可以通过方程DeltaG((X)(N)()(Z))(.)((Z)(')(-)(X)(')()) = 3.11 + 0. 40DeltaG(s)()((XZ))(.)((Z)(')(X)(')())很好地表示(±0.34千卡/摩尔)。DeltaG(s)()((XZ))(. )((Z)(')(X)(')())是封闭碱基对双峰的堆积能量。通过在上述方程右侧加上一个常数项δ = -0.3千卡/摩尔,II组凸起的自由能也可以以相同的精度预测。项δ代表由于位置简并性产生的稳定作用。一个类似的方程/模型应用于先前来自32个具有单碱基凸起的DNA片段的数据。它以类似的标准偏差预测了自由能差异。