Smith J E, Cooperman B S, Mitchell P
Department of Chemistry, University of Pennsylvania, Philadelphia 19104.
Biochemistry. 1992 Nov 10;31(44):10825-34. doi: 10.1021/bi00159a025.
Four previously undetermined sites of methylation are mapped in Escherichia coli 23S rRNA employing a novel combination of methods. First, using a double-isotope approach, the total number of methyl groups in 23S rRNA was determined to be 14.9 +/- 1.6. Second, hybridization of methyl-labeled rRNA to complementary DNA restriction fragments and PAGE analysis were used to purify RNA-DNA heteroduplexes and to quantify methyl groups within specific 23S rRNA fragments. Third, the methylated nucleosides in these fragments were identified and quantified using HPLC, confirming the presence of 14 methylation sites in 23S rRNA, four more than had been previously identified. In contrast, a similar set of analyses conducted on 16S rRNA gave evidence for 10 sites of methylation, at all approximate locations consistent with published 16S methylated nucleoside identities and locations. Selected regions of the 23S rRNA molecule containing previously unidentified methylated nucleosides were released by site-directed cleavage with ribonuclease H and isolated by PAGE. Sites of methylation within the RNA fragments were determined by classical oligonucleotide analyses. The four newly identified methylation sites in 23S rRNA are m2G-1835, m5C-1962, m6A-2503, and m2G at one of positions 2445-2447. Together with previously described sites of modification, these new sites form a group that is clustered in a current model for the three-dimensional organization of the 23S rRNA in the 50S ribosomal subunit, at a locus congruent with nucleotides previously implicated in ribosomal function.
利用一套全新的组合方法,在大肠杆菌23S核糖体RNA中确定了4个先前未知的甲基化位点。首先,采用双同位素方法,确定23S核糖体RNA中甲基基团的总数为14.9±1.6。其次,通过甲基标记的核糖体RNA与互补DNA限制性片段杂交及聚丙烯酰胺凝胶电泳(PAGE)分析,纯化RNA-DNA异源双链体,并对特定23S核糖体RNA片段中的甲基基团进行定量。第三,使用高效液相色谱法(HPLC)对这些片段中的甲基化核苷进行鉴定和定量,证实23S核糖体RNA中存在14个甲基化位点,比先前确定的多4个。相比之下,对16S核糖体RNA进行的一组类似分析表明有10个甲基化位点,其所有大致位置均与已发表的16S甲基化核苷的身份和位置一致。通过核糖核酸酶H进行定点切割,释放出23S核糖体RNA分子中包含先前未鉴定甲基化核苷的选定区域,并通过PAGE进行分离。通过经典的寡核苷酸分析确定RNA片段中的甲基化位点。23S核糖体RNA中4个新鉴定的甲基化位点分别是m2G-1835、m5C-1962、m6A-2503以及2445 - 2447位中的一个m2G。这些新位点与先前描述的修饰位点一起,形成了一个簇,在当前50S核糖体亚基中23S核糖体RNA三维结构模型里,位于与先前涉及核糖体功能的核苷酸一致的位点。