Vass J K, Maden B E
Eur J Biochem. 1978 Apr;85(1):241-7. doi: 10.1111/j.1432-1033.1978.tb12232.x.
We have studied the conformation of the 3' end of 18-S RNA from human, hamster and Xenopus laevis cells. The 3'-terminal oligonucleotide in a T1 ribonuclease digest of 18-S RNA from HeLa cells was identified, using a standard fingerprinting method. The sequence (G)-A-U-C-A-U-U-A, established by Eladari and Galibert for HeLa 18-S rRNA, was confirmed. An identical 3' terminus is present in hamster fibroblasts and Xenopus laevis cells. The ease of identification of this oligonucleotide has enabled us to quantify its molar yield relative to several other oligonucleotides, and hence to analyse the 3' terminus by several conformation probes. Its sensitivity to S1 nuclease, limited T1 ribonuclease digestion, bisulphite modification and carbodiimide modification was consistent with the terminal oligonucleotide being in a highly exposed conformation. The m6/2A-m6/2A-C-containing sequence of 18-S rRNA also appears to be in an exposed location on the basis of three of these probes.
我们研究了来自人类、仓鼠和非洲爪蟾细胞的18 - S RNA 3'端的构象。使用标准指纹图谱法,鉴定了来自HeLa细胞的18 - S RNA经T1核糖核酸酶消化后的3'端寡核苷酸。Eladari和Galibert确定的HeLa 18 - S rRNA的序列(G)-A-U-C-A-U-U-A得到了证实。仓鼠成纤维细胞和非洲爪蟾细胞中存在相同的3'末端。这种寡核苷酸易于鉴定,这使我们能够相对于其他几种寡核苷酸定量其摩尔产量,从而通过几种构象探针分析3'末端。它对S1核酸酶、有限的T1核糖核酸酶消化、亚硫酸氢盐修饰和碳二亚胺修饰的敏感性与末端寡核苷酸处于高度暴露的构象一致。基于其中三种探针,18 - S rRNA含m6/2A - m6/2A - C的序列似乎也处于暴露位置。