Andersen J, Delihas N, Hanas J S, Wu C W
Biochemistry. 1984 Nov 20;23(24):5752-9. doi: 10.1021/bi00319a013.
The structure of Xenopus laevis oocyte (Xlo) 5S ribosomal RNA has been probed with single-strand-specific ribonucleases T1, T2, and A with double-strand-specific ribonuclease V1 from cobra venom. The digestion of 5'- or 3'-labeled renatured 5S RNA samples followed by gel purification of the digested samples allowed the determination of primary cleavage sites. Results of these ribonuclease digestions provide support for the generalized 5S RNA secondary structural model derived from comparative sequence analysis. However, three putative single-stranded regions of the molecule exhibited unexpected V1 cuts, found at C36, U73, U76, and U102. These V1 cuts reflect additional secondary structural features of the RNA including A.G base pairs and support the extended base pairing in the stem containing helices IV and V which was proposed by Stahl et al. [Stahl, D. A., Luehrsen, K. R., Woese, C. R., & Pace, N. R. (1981) Nucleic Acids Res. 9, 6129-6137]. A conserved structure for helix V having a common unpaired uracil residue at Xlo position 84 is proposed for all eukaryotic 5S RNAs. Our results are compared with nuclease probes of other 5S RNAs.
非洲爪蟾卵母细胞(Xlo)5S核糖体RNA的结构已用单链特异性核糖核酸酶T1、T2和A以及眼镜蛇毒中的双链特异性核糖核酸酶V1进行了探测。对5′或3′标记的复性5S RNA样品进行消化,然后对消化后的样品进行凝胶纯化,从而确定主要切割位点。这些核糖核酸酶消化的结果为从比较序列分析得出的通用5S RNA二级结构模型提供了支持。然而,该分子的三个假定单链区域在C36、U73、U76和U102处出现了意外的V1切割。这些V1切割反映了RNA的其他二级结构特征,包括A·G碱基对,并支持了Stahl等人提出的包含螺旋IV和V的茎中的扩展碱基配对[Stahl, D. A., Luehrsen, K. R., Woese, C. R., & Pace, N. R. (1981) Nucleic Acids Res. 9, 6129 - 6137]。对于所有真核生物5S RNA,提出了螺旋V的保守结构,其在Xlo位置84处有一个共同的未配对尿嘧啶残基。我们的结果与其他5S RNA的核酸酶探测结果进行了比较。