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Identification of a new ribose methylation in the 18S rRNA of S. cerevisiae

机译:酿酒酵母18S rRNA中新的核糖甲基化的鉴定

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Methylation of ribose sugars at the 2'-OH group is one of the major chemical modifications in rRNA, and is catalyzed by snoRNA directed C/D box snoRNPs. Previous biochemical and computational analyses of the C/D box snoRNAs have identified and mapped a large number of 2'-OH ribose methylations in rRNAs. In the present study, we systematically analyzed ribose methylations of 18S rRNA in Saccharomyces cerevisiae, using mung bean nuclease protection assay and RP-HPLC. Unexpectedly, we identified a hitherto unknown ribose methylation at position G562 in the helix 18 of 5' central domain of yeast 18S rRNA. Furthermore, we identified snR40 as being responsible to guide snoRNP complex to catalyze G562 ribose methylation, which makes it only second snoRNA known so far to target three ribose methylation sites: Gm562, Gm1271 in 18S rRNA, and Um898 in 25S rRNA. Our sequence and mutational analysis of snR40 revealed that snR40 uses the same D' box and methylation guide sequence for both Gm562 and Gm1271 methylation. With the identification of Gm562 and its corresponding snoRNA, complete set of ribose methylations of 18S rRNA and their corresponding snoRNAs have finally been established opening great prospects to understand the physiological function of these modifications.
机译:2'-OH基上的核糖的甲基化是rRNA中的主要化学修饰之一,并且由snoRNA定向的C / D盒snoRNP催化。 C / D盒snoRNA的先前生化分析和计算分析已经鉴定并绘制了rRNA中大量2'-OH核糖甲基化的图。在本研究中,我们使用绿豆核酸酶保护试验和RP-HPLC系统分析了酿酒酵母中18S rRNA的核糖甲基化。出乎意料的是,我们在酵母18S rRNA的5'中央结构域的螺旋18中的G562位置上发现了迄今未知的核糖甲基化。此外,我们确定snR40负责引导snoRNP复合物催化G562核糖甲基化,这使得迄今为止仅已知第二个snoRNA靶向三个核糖甲基化位点:Gm562、18S rRNA中的Gm1271和25S rRNA中的Um898。我们对snR40的序列和突变分析表明,SnR40对Gm562和Gm1271甲基化使用相同的D'框和甲基化指导序列。通过鉴定Gm562及其相应的snoRNA,终于建立了18S rRNA的完整核糖甲基化及其相应的snoRNA的完整结构,为了解这些修饰的生理功能打开了广阔的前景。

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