Veldman G M, Klootwijk J, de Regt V C, Planta R J, Branlant C, Krol A, Ebel J P
Nucleic Acids Res. 1981 Dec 21;9(24):6935-52. doi: 10.1093/nar/9.24.6935.
We present the sequence of the 26S rRNA of the yeast Saccharomyces carlsbergensis as inferred from the gene sequence. The molecule is 3393 nucleotides long and consists of 48% G+C; 30 of the 43 methyl groups can be located in the sequence. Starting from the recently proposed structure of E. coli 23S rRNA (see ref. 25) we constructed a secondary structure model for yeast 26S rRNA. This structure is composed of 7 domains closed by long-range base pairings as n the bacterial counterpart. Most domains show considerable conservation of the overall structure; unpaired regions show extended sequence homology and the base-paired regions contain many compensating base pair changes. The extra length of the yeast molecule is due to a number of insertions in most of the domains, particularly in domain II. Domain VI, which is extremely conserved, is probably part of the ribosomal A site. alpha-Sarcin, which apparently inhibits the EF-1 dependent binding of aminoacyl-tRNA, causes a cleavage between position 3025 and 3026 in a conserved loop structure, just outside domain VI. Nearly all of the located methyl groups, like in E. coli, are present in domain II, V and VI and clustered to a certain extent mainly in regions with a strongly conserved primary structure. The only three methyl groups of 26S rRNA which are introduced relatively late during the processing are found in single stranded loops in domain VI very close to positions which have been shown in E. coli 23S rRNA to be at the interface of the ribosome.
我们根据基因序列推断出了卡尔斯伯酵母26S rRNA的序列。该分子长3393个核苷酸,G+C含量为48%;43个甲基中的30个可在序列中定位。从最近提出的大肠杆菌23S rRNA结构(见参考文献25)出发,我们构建了酵母26S rRNA的二级结构模型。此结构由7个结构域组成,通过长程碱基配对封闭,如同细菌中的对应结构。大多数结构域的整体结构具有相当程度的保守性;未配对区域显示出广泛的序列同源性,而碱基配对区域包含许多补偿性碱基对变化。酵母分子的额外长度是由于大多数结构域中存在一些插入片段,特别是在结构域II中。极其保守的结构域VI可能是核糖体A位点的一部分。α-肌动蛋白显然抑制氨酰-tRNA的EF-1依赖性结合,它在结构域VI外侧的一个保守环结构中的3025和3026位之间造成切割。与大肠杆菌一样,几乎所有定位的甲基都存在于结构域II、V和VI中,并且在一定程度上聚集在一级结构高度保守的区域。26S rRNA中仅有的三个在加工过程中相对较晚引入的甲基位于结构域VI的单链环中,非常靠近在大肠杆菌23S rRNA中已显示为核糖体界面的位置。