Labiris, B-1070 Bruxelles, Belgium.
Architecture et Réactivité de l'ARN, Institut de Biologie Moléculaire et Cellulaire du CNRS, Université de Strasbourg, F-67084, Strasbourg, France.
RNA. 2022 Sep;28(9):1185-1196. doi: 10.1261/rna.079131.122. Epub 2022 Jun 16.
A previous bioinformatic analysis predicted that the open reading frame of encodes an RNA methyltransferase of the SPOUT superfamily. Here we show that YsgA is the 2'--methyltransferase that targets position G2553 ( numbering) of the A-loop of 23S rRNA. This was shown by a combination of biochemical and mass spectrometry approaches using both rRNA extracted from wild-type or cells and in vitro synthesized rRNA. When the target G2553 is mutated, YsgA is able to methylate the ribose of adenosine. However, it cannot methylate cytidine nor uridine. The enzyme modifies free 23S rRNA but not the fully assembled ribosome nor the 50S subunit, suggesting that the modification occurs early during ribosome biogenesis. Nevertheless, ribosome subunits assembly is unaffected in a mutant strain. The crystal structure of the recombinant YsgA protein, combined with mutagenesis data, outlined in this article highlights a typical SPOUT fold preceded by an L7Ae/L30 (eL8/eL30 in a new nomenclature) amino-terminal domain.
先前的生物信息学分析预测,开放阅读框编码 SPOUT 超家族的 RNA 甲基转移酶。在这里,我们表明 YsgA 是靶向 23S rRNA A 环位置 G2553(编号)的 2'-甲基转移酶。这是通过使用从野生型或突变细胞提取的 rRNA 和体外合成的 rRNA 的组合生化和质谱方法来证明的。当靶标 G2553 发生突变时,YsgA 能够甲基化腺苷的核糖。然而,它不能甲基化胞嘧啶或尿嘧啶。该酶修饰游离的 23S rRNA,但不修饰完全组装的核糖体或 50S 亚基,表明修饰发生在核糖体生物发生的早期。然而,在突变菌株中,核糖体亚基组装不受影响。本文结合突变数据概述了重组 YsgA 蛋白的晶体结构,突出了一个典型的 SPOUT 折叠,前面是 L7Ae/L30(在新命名法中为 eL8/eL30)氨基末端结构域。