Nazar R N, Lo A C, Wildeman A G, Sitz T O
Nucleic Acids Res. 1983 Sep 10;11(17):5989-6001. doi: 10.1093/nar/11.17.5989.
The mammalian 5.8S rRNA contains a partially 2'-O-methylated uridylic acid residue at position 14 which is largely or entirely methylated in the cytoplasm (Nazar, R.N., Sitz, T.O. and Sommers, K.D. (1980) J. Mol. Biol. 142, 117-121). The effect of this methylation on the 5.8S RNA structure and 5.8-28S rRNA junction was investigated using both chemical and physical approaches. Electrophoretic studies indicated that the free 5.8S rRNA can take on at least two different conformations and that the 2'-O-methylation at U14 restricts the molecule to the more hydrodynamically open form. Structural studies using limited pancreatic or T1 ribonuclease digestion indicated that the methylated conformation was more susceptible to digestion, consistent with a more open tertiary structure. Modification-exclusion studies indicated that the first 29 nucleotides at the 5' end and residues 140 through 158 at the 3' end affect the 5.8S-28S rRNA interaction, supporting previous suggestions that the 5.8S RNA interacts with its cognate high molecular weight component through its termini. These results also suggested that the 2'-O-methylated uridylic acid residue plays a role in the 5.8S-28S rRNA interaction and thermal denaturation studies confirmed this by showing that methylation destabilizes the 5.8S-28S rRNA junction. The 5.8-28S rRNA interaction appears to be more complex than previously believed.
哺乳动物的5.8S核糖体RNA在第14位含有一个部分2'-O-甲基化的尿苷酸残基,该残基在细胞质中大部分或完全甲基化(纳扎尔,R.N.,西茨,T.O.和萨默斯,K.D.(1980年)《分子生物学杂志》142卷,117 - 121页)。使用化学和物理方法研究了这种甲基化对5.8S核糖体RNA结构和5.8 - 28S核糖体RNA连接的影响。电泳研究表明,游离的5.8S核糖体RNA可以呈现至少两种不同的构象,并且U14位的2'-O-甲基化将分子限制为更具流体动力学开放性的形式。使用有限的胰核糖核酸酶或T1核糖核酸酶消化进行的结构研究表明,甲基化构象更容易被消化,这与更开放的三级结构一致。修饰排除研究表明,5'端的前29个核苷酸和3'端的140至158位残基影响5.8S - 28S核糖体RNA的相互作用,支持了先前的观点,即5.8S核糖体RNA通过其末端与其同源高分子量成分相互作用。这些结果还表明,2'-O-甲基化的尿苷酸残基在5.8S - 28S核糖体RNA相互作用中起作用,热变性研究通过表明甲基化使5.8S - 28S核糖体RNA连接不稳定证实了这一点。5.8 - 28S核糖体RNA的相互作用似乎比以前认为的更为复杂。