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Overexpression of Two Different GTPases Rescues a Null Mutation in a Heat-Induced rRNA Methyltransferase

机译:两种不同的GTPases的过表达挽救了热诱导的rRNA甲基转移酶的空突变。

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摘要

The Escherichia coli RrmJ (FtsJ) heat shock protein functions as an rRNA methyltransferase that modifies position U2552 of 23S rRNA in intact 50S ribosomal subunits. An in-frame deletion of the rrmJ (ftsJ) gene leads to severe growth disadvantages under all temperatures tested and causes significant accumulation of ribosomal subunits at the expense of functional 70S ribosomes. To investigate whether overexpression of other E. coli genes can restore the severe growth defect observed in rrmJ null mutants, we constructed an overexpression library from the rrmJ deletion strain and cloned and identified the E. coli genes that were capable of rescuing the rrmJ mutant phenotype. Our intention was to identify other methylases whose specificities overlapped enough with that of RrmJ to allow complementation when overexpressed. To our great surprise, no methylases were found by this method; rather, two small GTPases, Obg (YhbZ) and EngA, when overexpressed in the rrmJ deletion strains, were found to restore the otherwise severely impaired ribosome assembly process and/or stability of 70S ribosomes. 50S ribosomal subunits prepared from these overexpressing strains were shown to still serve as in vitro substrates for purified RrmJ, indicating that the 23S rRNA likely was still lacking the highly conserved Um2552 modification. The apparent lack of this modification, however, no longer caused ribosome defects or a growth disadvantage. Massive overexpression of another related small GTPase, Era, failed to rescue the growth defects of an rrmJ strain. These findings suggest a hitherto unexpected connection between rRNA methylation and GTPase function, specifically that of the two small GTPases Obg and EngA.
机译:大肠杆菌RrmJ(FtsJ)热激蛋白起rRNA甲基转移酶的作用,修饰完整的50S核糖体亚基中23S rRNA的U2552位置。在所有测试温度下,rrmJ(ftsJ)基因的框内缺失都会导致严重的生长缺陷,并导致核糖体亚基大量积累,但会破坏功能性70S核糖体。为了研究其他大肠杆菌基因的过量表达是否可以恢复在rrmJ null突变体中观察到的严重生长缺陷,我们从rrmJ缺失菌株构建了一个过量表达文库,并克隆并鉴定了能够拯救rrmJ突变表型的大肠杆菌基因。 。我们的意图是鉴定其他甲基化酶,这些甲基化酶的特异性与RrmJ的特异性足够重叠,以便在过表达时进行互补。令我们惊讶的是,这种方法没有发现甲基化酶。相反,当在rrmJ缺失菌株中过表达时,发现了两个小的GTPases,Obg(YhbZ)和EngA,可以恢复原本严重受损的核糖体装配过程和/或70S核糖体的稳定性。从这些过表达的菌株制备的50S核糖体亚基显示仍可作为纯化RrmJ的体外底物,表明23S rRNA可能仍缺乏高度保守的Um2552修饰。然而,显然缺乏这种修饰不再导致核糖体缺陷或生长不利。另一个相关的小GTP酶Era的大量过量表达未能挽救rrmJ菌株的生长缺陷。这些发现表明,迄今为止,rRNA甲基化与GTPase功能之间存在着前所未有的联系,特别是两个小GTPases Obg和EngA之间的联系。

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