Alkemar Gunnar, Nygård Odd
Cell Biology Unit, Natural Science Section, Södertörns högskola, S-141 89 Huddinge, Sweden.
RNA. 2004 Mar;10(3):403-11. doi: 10.1261/rna.5135204.
The 18S rRNA of the small eukaryotic ribosomal subunit contains several expansion segments. Electron microscopy data indicate that two of the largest expansion segments are juxtaposed in intact 40S subunits, and data from phylogenetic sequence comparisons indicate that these two expansion segments contain complementary sequences that could form a direct tertiary interaction on the ribosome. We have investigated the secondary structure of the two expansion segments in the region around the putative tertiary interaction. Ribosomes from yeast, wheat, and mouse-three organisms representing separate eukaryotic kingdoms-were isolated, and the structure of ES3 and part of the ES6 region were analyzed using the single-strand-specific chemical reagents CMCT and DMS and the double-strand-specific ribonuclease V1. The modification patterns were analyzed by primer extension and gel electrophoresis on an ABI 377 automated DNA sequencer. The investigated sequences were relatively exposed to chemical and enzymatic modification. This is in line with their indicated location on the surface at the solvent side of the subunit. The complementary ES3 and ES6 sequences were clearly inaccessible to single-strand modification, but available for cleavage by double-strand-specific RNase V1. The results are compatible with a direct helical interaction between bases in ES3 and ES6. Almost identical results were obtained with ribosomes from the three organisms investigated.
真核生物小核糖体亚基的18S rRNA包含几个扩展片段。电子显微镜数据表明,两个最大的扩展片段在完整的40S亚基中并列,系统发育序列比较数据表明,这两个扩展片段包含互补序列,可能在核糖体上形成直接的三级相互作用。我们研究了假定三级相互作用区域中两个扩展片段的二级结构。分离了来自酵母、小麦和小鼠这三种代表不同真核生物界的生物体的核糖体,并使用单链特异性化学试剂CMCT和DMS以及双链特异性核糖核酸酶V1分析了ES3和ES6区域部分的结构。通过引物延伸和在ABI 377自动DNA测序仪上进行凝胶电泳来分析修饰模式。所研究的序列相对容易受到化学和酶促修饰的影响。这与它们在亚基溶剂侧表面的指定位置一致。互补的ES3和ES6序列明显不能被单链修饰,但可被双链特异性核糖核酸酶V1切割。结果与ES3和ES6中的碱基之间的直接螺旋相互作用一致。对所研究的三种生物体的核糖体获得了几乎相同的结果。