Herr W, Noller H F
Biochemistry. 1978 Jan 24;17(2):307-15. doi: 10.1021/bi00595a018.
Nucleotide sequences around kethoxal-reactive guanine residues of 23S RNA in 50S ribosomal subunits have been determined. By use of the diagonal paper electrophoresis method )Noller, H.F. (1974), Biochemistry 13, 4694-4703), 41 ribonuclease T1 oligonucleotides, originating from about 25 sites, were identified and sequenced. These sites are single stranded and accessible in free 50S subunits, and are thus potential sites for interaction with functional ligands during protein synthesis. Examination of these sequences for potential intermolecular base-pairing reveals the following: (1) There are 19 possible complementary combinations between exposed sequences in 16S and 23S RNA containing more than 4 base pairs: 15 containing 5 base pairs and 4 containing 6 base pairs. Nine of these complementary combinations contain 16S RNA sequences which we have previously shown to be protected from kethoxall by 50S subunits (Chapman, N.M., and Noller, H.F. (1977), J. Mol. Biol. 109, 131-149). (2) One of the exposed sites in 23S RNA has a sequence which is complementary to the invariant GT psi CR sequence in tRNA.
已确定了50S核糖体亚基中23S RNA的乙二醛反应性鸟嘌呤残基周围的核苷酸序列。利用对角线纸电泳法(诺勒,H.F.(1974年),《生物化学》13卷,4694 - 4703页),鉴定并测序了源自约25个位点的41个核糖核酸酶T1寡核苷酸。这些位点是单链的,在游离的50S亚基中可及,因此是蛋白质合成过程中与功能性配体相互作用的潜在位点。对这些序列进行潜在分子间碱基配对的检查揭示了以下情况:(1)在16S和23S RNA的暴露序列之间有19种可能的互补组合,包含超过4个碱基对:15种包含5个碱基对,4种包含6个碱基对。这些互补组合中有9种包含16S RNA序列,我们之前已表明这些序列在50S亚基存在时可免受乙二醛影响(查普曼,N.M.,和诺勒,H.F.(1977年),《分子生物学杂志》109卷,131 - 149页)。(2)23S RNA中的一个暴露位点具有与tRNA中不变的GTψCR序列互补的序列。