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对由寡聚体序列d[GGATAC(X)4GTATCC](X = A、T、G、C)形成的DNA发夹的熔解转变进行分析。

Analysis of melting transitions of the DNA hairpins formed from the oligomer sequences d[GGATAC(X)4GTATCC] (X = A, T, G, C).

作者信息

Paner T M, Amaratunga M, Doktycz M J, Benight A S

机构信息

Department of Chemistry, University of Illinois, Chicago 60680.

出版信息

Biopolymers. 1990 Dec;29(14):1715-34. doi: 10.1002/bip.360291405.

Abstract

Optical melting transitions of the short DNA hairpins formed from the self-complementary DNA oligomers d[GGATACX4GTATCC] where X = A, T, G, or C measured in 100 mM NaCl are presented. A significant dependence of the melting transitions on loop sequence is observed and transition temperatures, tm, of the hairpins vary from 58.3 degrees C for the T4 loop hairpin to 55.3 degrees C for the A4 loop. A nearest-neighbor sequence-dependent theoretical algorithm for calculating melting curves of DNA hairpins is presented and employed to analyze the experimental melting transitions. Experimental melting curves were fit by adjustment of a single theoretical parameter, Fend(n), the weighting function for a hairpin loop comprised of n single-strand bases. Empirically determined values of Fend(n) provide an evaluation of the free-energy of hairpin loop formation and stability. Effects of heterogeneous nearest-neighbor sequence interactions in the duplex stem on hairpin loop formation were investigated by evaluating Fend(n) in individual fitting procedures using two of the published sets of nearest-neighbor stacking interactions in DNA evaluated in 100 mM NaCl and given by Wartell and Benight, 1985. In all cases, evaluated values of Fend(n) were obtained that provided exact theoretical predictions of the experimental transitions. Results of the evaluations indicate: (1) Evaluated free-energies of hairpin loop formation are only slightly dependent on loop sequences examined. At the transition temperature, Tm, the free-energy of forming a loop of four bases is approximately equal for T4, G4, or C4 loops and varies from 3.9 to 4.8 kcal/mole depending on the set of nearest-neighbor interactions employed in the evaluations. This result suggests, in light of the observed differences in stability between the T4, G4, and C4 loop hairpins, that sequence-dependent interactions between base residues of the loop are most likely not the source of the enhanced stability of a T4 loop.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本文展示了由自互补DNA寡聚物d[GGATACX4GTATCC](其中X = A、T、G或C)形成的短DNA发夹在100 mM NaCl中的光学熔解转变。观察到熔解转变对环序列有显著依赖性,发夹的转变温度tm从T4环发夹的58.3℃到A4环的55.3℃不等。提出了一种用于计算DNA发夹熔解曲线的最近邻序列依赖性理论算法,并用于分析实验熔解转变。通过调整单个理论参数Fend(n)(由n个单链碱基组成的发夹环的加权函数)来拟合实验熔解曲线。根据经验确定的Fend(n)值可评估发夹环形成的自由能和稳定性。通过在单独的拟合程序中使用1985年Wartell和Benight给出的在100 mM NaCl中评估的两组已发表的DNA最近邻堆积相互作用来评估双链茎中异质最近邻序列相互作用对发夹环形成的影响。在所有情况下,都获得了Fend(n)的评估值,这些值提供了对实验转变的精确理论预测。评估结果表明:(1)评估的发夹环形成自由能仅略微依赖于所检查的环序列。在转变温度Tm下,对于T4、G4或C4环,形成四个碱基环的自由能大致相等,根据评估中使用的最近邻相互作用组,其范围为3.9至4.8千卡/摩尔。鉴于观察到T4、G4和C4环发夹之间稳定性的差异,这一结果表明环碱基残基之间的序列依赖性相互作用很可能不是T4环增强稳定性的来源。(摘要截断于400字)

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