Nazar R N, Sitz T O, Busch H
J Biol Chem. 1975 Nov 25;250(22):8591-7.
The nucleotide sequence of ribosomal 5.8 S RNA (also known as 7 S or 5.5 S rRNA) from Novikoff hepatoma ascites cells has been determined to be (see article). Estimations of the secondary structure based upon maximized base pairing and the fragments of partial ribonuclease digestion indicate that there may be five base-paired regions in the molecule, three forming a folding of the termini and two forming secondary hairpin loops. The sequence of Novikoff hepatoma 5.8 S rRNA is about 75% homologous with that of yeast 5.8 S rRNA (Rubin, G.M. (1973) J. Biol. Chem. 248, 3860-3875) and similar models for secondary structure are proposed. Both models contain a very stable G-C rich hairpin loop (residues 116 to 138), a less stable A-U-rich hairpin loop (residues 64 to 91) and two symmetrical bulges (residues 15 to 25 and 40 to 44).
已确定来自诺维科夫肝癌腹水细胞的核糖体5.8 S RNA(也称为7 S或5.5 S rRNA)的核苷酸序列(见文章)。基于最大程度碱基配对和部分核糖核酸酶消化片段对二级结构的估计表明,该分子中可能存在五个碱基配对区域,其中三个形成末端折叠,两个形成二级发夹环。诺维科夫肝癌5.8 S rRNA的序列与酵母5.8 S rRNA的序列约75%同源(鲁宾,G.M.(1973年)《生物化学杂志》248,3860 - 3875),并提出了类似的二级结构模型。两个模型都包含一个非常稳定的富含G - C的发夹环(第116至138位残基)、一个稳定性稍差的富含A - U的发夹环(第64至91位残基)以及两个对称凸起(第15至25位残基和第40至44位残基)。