Vaughn J C, Sperbeck S J, Ramsey W J, Lawrence C B
Nucleic Acids Res. 1984 Oct 11;12(19):7479-502. doi: 10.1093/nar/12.19.7479.
The phylogenetic approach (ref. 1) has been utilized in construction of a universal 5.8S rRNA secondary structure model, in which about 65% of the residues exist in paired structures. Conserved nucleotides primarily occupy unpaired regions. Multiple compensating base changes are demonstrated to be present in each of the five postulated helices, thereby forming a major basis for their proof. The results of chemical and enzymatic probing of 5.8S rRNAs (ref. 13, 32) are fully consistent with, and support, our model. This model differs in several ways from recently proposed 5.8S rRNA models (ref. 3, 4), which are discussed. Each of the helices in our model has been extended to the corresponding bacterial, chloroplast and mitochondrial sequences, which are demonstrated to be positionally conserved by alignment with their eukaryotic counterparts. This extension is also made for the base paired 5.8S/28S contact points, and their prokaryotic and organelle counterparts. The demonstrated identity of secondary structure in these diverse molecules strongly suggests that they perform equivalent functions in prokaryotic and eukaryotic ribosomes.
系统发育方法(参考文献1)已被用于构建通用的5.8S rRNA二级结构模型,其中约65%的残基存在于配对结构中。保守核苷酸主要占据未配对区域。已证明在五个假定的螺旋结构中的每一个中都存在多个补偿性碱基变化,从而构成了它们得以证实的主要依据。对5.8S rRNAs进行化学和酶促探测的结果(参考文献13、32)与我们的模型完全一致并提供了支持。该模型在几个方面与最近提出的5.8S rRNA模型(参考文献3、4)不同,文中对此进行了讨论。我们模型中的每个螺旋结构都已扩展至相应的细菌、叶绿体和线粒体序列,通过与它们的真核对应序列比对,证明这些序列在位置上是保守的。对于碱基配对的5.8S/28S接触点及其原核和细胞器对应物也进行了这样的扩展。这些不同分子中二级结构的一致性强烈表明它们在原核和真核核糖体中发挥着等效功能。