Sarge K D, Maxwell E S
Department of Biochemistry, North Carolina State University, Raleigh 27695-7622.
Biochim Biophys Acta. 1991 Jan 17;1088(1):57-70. doi: 10.1016/0167-4781(91)90153-d.
Eukaryotic 5S rRNA hybridizes specifically with 18S rRNA in vitro to form a stable intermolecular RNA:RNA hybrid. We have used 5S rRNA/18S rRNA fragment hybridization studies coupled with ribonuclease digestion and primer extension/chain termination analysis of 5S rRNA:18S rRNA hybrids to more completely map those mouse 5S rRNA and 18S rRNA sequences responsible for duplex formation. Fragment hybridization analysis has defined a 5'-terminal region of 5S rRNA (nucleotides 6-27) which base-pairs with two independent sequences in 18S rRNA designated Regions 1 (nucleotides 1157-1180) and 2 (nucleotides 1324-1339). Ribonuclease digestion of isolated 5S rRNA:18S rRNA hybrids with both single-strand- and double-strand-specific nucleases supports the involvement of this 5'-terminal 5S rRNA sequence in 18S rRNA hybridization. Primer extension/chain termination analysis of isolated 5S rRNA:18S rRNA hybrids confirms the base-pairing of 5S rRNA to the designated Regions 1 and 2 of 18S rRNA. Using these results, 5S rRNA:18S rRNA intermolecular hybrid structures are proposed. Comparative sequence analysis revealed the conservation of these hybrid structures in higher eukaryotes and the same but smaller core hybrid structures in lower eukaryotes and prokaryotes. This suggests that the 5S rRNA:16S/18S rRNA hybrids have been conserved in evolution for ribosome function.
真核生物5S核糖体RNA在体外与18S核糖体RNA特异性杂交,形成稳定的分子间RNA:RNA杂交体。我们利用5S核糖体RNA/18S核糖体RNA片段杂交研究,结合核糖核酸酶消化以及5S核糖体RNA:18S核糖体RNA杂交体的引物延伸/链终止分析,更全面地绘制出负责双链形成的小鼠5S核糖体RNA和18S核糖体RNA序列。片段杂交分析确定了5S核糖体RNA的5'端区域(核苷酸6 - 27),它与18S核糖体RNA中两个独立的序列碱基配对,这两个序列分别称为区域1(核苷酸1157 - 1180)和区域2(核苷酸1324 - 1339)。用单链和双链特异性核酸酶对分离出的5S核糖体RNA:18S核糖体RNA杂交体进行核糖核酸酶消化,支持了这个5'端5S核糖体RNA序列参与18S核糖体RNA杂交。对分离出的5S核糖体RNA:18S核糖体RNA杂交体进行引物延伸/链终止分析,证实了5S核糖体RNA与18S核糖体RNA指定的区域1和区域2碱基配对。利用这些结果,提出了5S核糖体RNA:18S核糖体RNA分子间杂交结构。比较序列分析揭示了这些杂交结构在高等真核生物中的保守性,以及在低等真核生物和原核生物中相同但较小的核心杂交结构。这表明5S核糖体RNA:16S/18S核糖体RNA杂交体在进化过程中因核糖体功能而得以保留。