Cecchini J P, Miassod R
Eur J Biochem. 1979 Jul;98(1):203-14. doi: 10.1111/j.1432-1033.1979.tb13178.x.
The methylation of cytoplasmic ribosomal RNA of cultured sycamore cells (Acer pseudoplatanus L.) was investigated. Labelled 17-S and 26-S rRNA were prepared from cells that had been incubated with either [32P]phosphate, [Me-3H]methionine or [Me-14C]methionine. Ion-exchange resin chromatography of 0.3 M KOH or 1 M HCl hydrolysates and two-dimensional chromatographic analyses of phosphodiesterase plus phosphatase digests of 17-S and 26-S rRNA were performed. 17-S and 26-S rRNA contain 49 and 91 methyl groups per molecule, respectively. These values were verified in sevemral ways. The high degree of methylation of sycamore rRNA, particularly for the 26-S rRNA, contrasts with the situation in all other investigated organisms. Several methylated bases were identified. 7-Methylguanine and 5-methylcytosine both occur in 17-S and 26-S rRNA. N6-Methyladenine and N6,N6-dimethyladenine are restricted to the 17-S rRNA while 3-methyluracil and 1-methyladenine occur in the 26-S rRNA. One hypermodified uridine was also tentatively identified in the small rRNA. In 17-S rRNA, there is one copy of 7-methylguanine, N6-methyladenine and hypermodified uridine and two copies of N6,N6-dimethyladenine. 3-Methyluracil, 1-methyladenine and 5-methylcytosine occur twice, twice and three times, respectively, in 26-S rRNA. 7-Methylguanine and 5-methylcytosine are only in submolar amounts in the 26-S and 17-S rRNA, respectively. There are 40 +/- 2 and 83 +/- 3 2'-O-methylriboses per 17-S and 26-S rRNA molecule, respectively. In addition to the four 2'-O-methylnucleosides, one 2'-O-methylpseudouridine is present in the 17-S rRNA. Several lines of evidence argues for a non-random distribution of the methylriboses. In particular, one and seven Nm-Nm-Np structures occur in the 17-S and 26-S rRNA, respectively. The data are discussed comparatively with the methylation pattern of Escherichia coli, yeast and HeLa cell rRNA.
对培养的梧桐细胞(槭树)细胞质核糖体RNA的甲基化进行了研究。标记的17 - S和26 - S rRNA是从用[32P]磷酸盐、[Me - 3H]甲硫氨酸或[Me - 14C]甲硫氨酸孵育过的细胞中制备的。对0.3 M KOH或1 M HCl水解产物进行离子交换树脂色谱分析,并对17 - S和26 - S rRNA的磷酸二酯酶加磷酸酶消化产物进行二维色谱分析。17 - S和26 - S rRNA每分子分别含有49个和91个甲基基团。这些值通过几种方式得到了验证。梧桐rRNA的高度甲基化,特别是26 - S rRNA的甲基化,与所有其他已研究生物的情况形成对比。鉴定出了几种甲基化碱基。7 - 甲基鸟嘌呤和5 - 甲基胞嘧啶在17 - S和26 - S rRNA中均有出现。N6 - 甲基腺嘌呤和N6,N6 -二甲基腺嘌呤仅限于17 - S rRNA,而3 - 甲基尿嘧啶和1 - 甲基腺嘌呤出现在26 - S rRNA中。在小rRNA中还初步鉴定出一种超修饰尿苷。在17 - S rRNA中,有一个7 - 甲基鸟嘌呤、N6 - 甲基腺嘌呤和超修饰尿苷的拷贝,以及两个N6,N6 -二甲基腺嘌呤的拷贝。3 - 甲基尿嘧啶、1 - 甲基腺嘌呤和5 - 甲基胞嘧啶在26 - S rRNA中分别出现两次、两次和三次。7 - 甲基鸟嘌呤和5 - 甲基胞嘧啶在26 - S和17 - S rRNA中分别仅以亚摩尔量存在。每17 - S和26 - S rRNA分子分别有40±2个和83±3个2'-O -甲基核糖。除了四种2'-O -甲基核苷外,17 - S rRNA中还存在一种2'-O -甲基假尿苷。几条证据表明甲基核糖存在非随机分布。特别是,17 - S和26 - S rRNA中分别出现了一个和七个Nm - Nm - Np结构。将这些数据与大肠杆菌、酵母和HeLa细胞rRNA的甲基化模式进行了比较讨论。