Buchhaupt Markus, Sharma Sunny, Kellner Stefanie, Oswald Stefanie, Paetzold Melanie, Peifer Christian, Watzinger Peter, Schrader Jens, Helm Mark, Entian Karl-Dieter
DECHEMA Research Institute, Biochemical Engineering, Frankfurt am Main, Germany.
Institute for Molecular Biosciences, Johann-Wolfgang Goethe University, Frankfurt am Main, Germany.
PLoS One. 2014 Feb 28;9(2):e89640. doi: 10.1371/journal.pone.0089640. eCollection 2014.
Ribosome heterogeneity is of increasing biological significance and several examples have been described for multicellular and single cells organisms. In here we show for the first time a variation in ribose methylation within the 18S rRNA of Saccharomyces cerevisiae. Using RNA-cleaving DNAzymes, we could specifically demonstrate that a significant amount of S. cerevisiae ribosomes are not methylated at 2'-O-ribose of A100 residue in the 18S rRNA. Furthermore, using LC-UV-MS/MS of a respective 18S rRNA fragment, we could not only corroborate the partial methylation at A100, but could also quantify the methylated versus non-methylated A100 residue. Here, we exhibit that only 68% of A100 in the 18S rRNA of S.cerevisiae are methylated at 2'-O ribose sugar. Polysomes also contain a similar heterogeneity for methylated Am100, which shows that 40S ribosome subunits with and without Am100 participate in translation. Introduction of a multicopy plasmid containing the corresponding methylation guide snoRNA gene SNR51 led to an increased A100 methylation, suggesting the cellular snR51 level to limit the extent of this modification. Partial rRNA modification demonstrates a new level of ribosome heterogeneity in eukaryotic cells that might have substantial impact on regulation and fine-tuning of the translation process.
核糖体异质性具有越来越重要的生物学意义,在多细胞和单细胞生物中已有多个实例被描述。在此我们首次展示了酿酒酵母18S rRNA内核糖甲基化的变化。使用RNA切割脱氧核酶,我们能够特异性地证明,大量酿酒酵母核糖体在18S rRNA的A100残基的2'-O-核糖处未被甲基化。此外,通过对相应18S rRNA片段进行液相色谱-紫外-串联质谱分析,我们不仅证实了A100处的部分甲基化,还能够对甲基化与未甲基化的A100残基进行定量。在此,我们发现酿酒酵母18S rRNA中只有68%的A100在2'-O核糖糖处被甲基化。多核糖体在甲基化的Am100方面也存在类似的异质性,这表明含有和不含有Am100的40S核糖体亚基都参与了翻译过程。引入含有相应甲基化指导小核仁RNA基因SNR51的多拷贝质粒导致A100甲基化增加,这表明细胞内snR51水平限制了这种修饰的程度。部分rRNA修饰展示了真核细胞中核糖体异质性的一个新水平,这可能对翻译过程的调控和微调产生重大影响。