Gigova Andriana, Duggimpudi Sujitha, Pollex Tim, Schaefer Matthias, Koš Martin
Biochemistry Center and Cluster of Excellence CellNetworks, University of Heidelberg, 69120 Heidelberg, Germany.
Division of Epigenetics, DKFZ-ZMBH Alliance, German Cancer Research Center, 69120 Heidelberg, Germany.
RNA. 2014 Oct;20(10):1632-44. doi: 10.1261/rna.043398.113. Epub 2014 Aug 14.
In all three domains of life ribosomal RNAs are extensively modified at functionally important sites of the ribosome. These modifications are believed to fine-tune the ribosome structure for optimal translation. However, the precise mechanistic effect of modifications on ribosome function remains largely unknown. Here we show that a cluster of methylated nucleotides in domain IV of 25S rRNA is critical for integrity of the large ribosomal subunit. We identified the elusive cytosine-5 methyltransferase for C2278 in yeast as Rcm1 and found that a combined loss of cytosine-5 methylation at C2278 and ribose methylation at G2288 caused dramatic ribosome instability, resulting in loss of 60S ribosomal subunits. Structural and biochemical analyses revealed that this instability was caused by changes in the structure of 25S rRNA and a consequent loss of multiple ribosomal proteins from the large ribosomal subunit. Our data demonstrate that individual RNA modifications can strongly affect structure of large ribonucleoprotein complexes.
在生命的所有三个域中,核糖体RNA在核糖体功能重要位点被广泛修饰。这些修饰被认为是对核糖体结构进行微调以实现最佳翻译。然而,修饰对核糖体功能的确切机制影响在很大程度上仍然未知。在这里,我们表明25S rRNA结构域IV中的一簇甲基化核苷酸对于大核糖体亚基的完整性至关重要。我们鉴定出酵母中C2278的难以捉摸的胞嘧啶-5甲基转移酶为Rcm1,并发现C2278处胞嘧啶-5甲基化和G2288处核糖甲基化的联合缺失导致了显著的核糖体不稳定性,导致60S核糖体亚基的丢失。结构和生化分析表明,这种不稳定性是由25S rRNA结构的变化以及随之而来的大核糖体亚基中多种核糖体蛋白的丢失引起的。我们的数据表明,单个RNA修饰可以强烈影响大型核糖核蛋白复合物的结构。