Michot B, Bachellerie J P, Raynal F
Nucleic Acids Res. 1982 Sep 11;10(17):5273-83. doi: 10.1093/nar/10.17.5273.
We present the sequence of the 5' terminal 585 nucleotides of mouse 28S rRNA as inferred from the DNA sequence of a cloned gene fragment. The comparison of mouse 28S rRNA sequence with its yeast homolog, the only known complete sequence of eukaryotic nucleus-encoded large rRNA (see ref. 1, 2) reveals the strong conservation of two large stretches which are interspersed with completely divergent sequences. These two blocks of homology span the two segments which have been recently proposed to participate directly in the 5.8S-large rRNA complex in yeast (see ref. 1) through base-pairing with both termini of 5.8S rRNA. The validity of the proposed structural model for 5.8S-28S rRNA complex in eukaryotes is strongly supported by comparative analysis of mouse and yeast sequences: despite a number of mutations in 28S and 5.8S rRNA sequences in interacting regions, the secondary structure that can be proposed for mouse complex is perfectly identical with yeast's, with all the 41 base-pairings between the two molecules maintained through 11 pairs of compensatory base changes. The other regions of the mouse 28S rRNA 5'terminal domain, which have extensively diverged in primary sequence, can nevertheless be folded in a secondary structure pattern highly reminiscent of their yeast' homolog. A minor revision is proposed for mouse 5.8S rRNA sequence.
我们展示了从小鼠28S rRNA 5'末端585个核苷酸的序列,该序列是根据克隆基因片段的DNA序列推断出来的。将小鼠28S rRNA序列与其酵母同源物(真核细胞核编码的大rRNA唯一已知的完整序列,见参考文献1、2)进行比较,发现有两个大的区域高度保守,其间散布着完全不同的序列。这两个同源区域跨越了最近有人提出的在酵母中通过与5.8S rRNA的两个末端碱基配对而直接参与5.8S - 大rRNA复合体形成的两个片段(见参考文献1)。小鼠和酵母序列的比较分析有力地支持了真核生物中5.8S - 28S rRNA复合体所提出的结构模型的有效性:尽管在相互作用区域的28S和5.8S rRNA序列中有许多突变,但为小鼠复合体提出的二级结构与酵母的完全相同,两个分子之间的41个碱基对通过11对补偿性碱基变化得以维持。小鼠28S rRNA 5'末端结构域的其他区域,其一级序列有很大差异,但仍能折叠成与酵母同源物高度相似的二级结构模式。我们对小鼠5.8S rRNA序列提出了一个小的修订。