Sankofff D, Morin A M, Cederhren R J
Can J Biochem. 1978 Jun;56(6):440-3. doi: 10.1139/o78-068.
We have applied the Pipas-McMahon algorithm based on free energy calculations to the search for a 5S RNA base-pair structure common to all known sequences. We find that a 'Y' shaped model is consistently among the structures having the lowest free energy using 5S RNA sequences from either eukaryotic or prokaryotic sources. Compaison of this 'Y' structure with models which have recently been proposed show these models to be remarkably similar, and the minor differences are explicable based on the technique used to obtain the model. That prokaryotic and eukaryotic 5S RNA can adopt a similar secondary structure is strong support for its resistance to change during evolution.
我们已将基于自由能计算的皮帕斯 - 麦克马洪算法应用于寻找所有已知序列共有的5S RNA碱基对结构。我们发现,使用来自真核生物或原核生物来源的5S RNA序列时,“Y”形模型始终处于自由能最低的结构之中。将这种“Y”结构与最近提出的模型进行比较,结果表明这些模型非常相似,并且基于获得模型所使用的技术,这些微小差异是可以解释的。原核生物和真核生物的5S RNA能够采用相似的二级结构,这有力地支持了其在进化过程中抗变化的特性。