Leffers H, Andersen A H
Institute of Medical Biochemistry, Aarhus University, Denmark.
Nucleic Acids Res. 1993 Mar 25;21(6):1449-55. doi: 10.1093/nar/21.6.1449.
The primary structure of 28S ribosomal RNA constitutes a conserved core which is similar among most 23S-like rRNAs and expansion segments which occur at specific positions in the sequence. The expansion segments account for most of the size difference between prokaryotic (archaeal and eubacterial) and eukaryotic rRNAs and they exhibit a sequence variation which is unique among rRNAs. We have investigated the sequence variation of one of the expansion segments, V8, by sequencing a total of 111 V8 segments from 9 different human cell lines and tissues and have found 35 different variants. The variation occur mainly at two 'hot spots' which are separated by 170 nucleotides in the primary sequence but are neighbours in the secondary structure. The sequence of V8 segments varies both within and between human cell lines and tissues. The implications for the evolution of the eukaryotic 28S rRNA are discussed together with possible functions of the expansion segments. We also present a secondary structure model for the V8 segment based on comparative sequence analysis and chemical and enzymatic foot printing.
28S核糖体RNA的一级结构构成一个保守核心,该核心在大多数23S样rRNA中相似,且在序列的特定位置存在扩展片段。扩展片段占原核生物(古细菌和真细菌)与真核生物rRNA大小差异的大部分,并且它们表现出rRNA中独特的序列变异。我们通过对来自9种不同人类细胞系和组织的总共111个V8片段进行测序,研究了其中一个扩展片段V8的序列变异,发现了35种不同的变体。变异主要发生在两个“热点”,这两个热点在一级序列中相隔170个核苷酸,但在二级结构中是相邻的。V8片段的序列在人类细胞系和组织内部以及之间均有变化。讨论了真核生物28S rRNA进化的意义以及扩展片段的可能功能。我们还基于比较序列分析以及化学和酶促足迹法提出了V8片段的二级结构模型。