UMR8261 (CNRS-Université Paris Diderot), Institut de Biologie Physico-Chimique, 13 rue Pierre et Marie Curie, 75005 Paris, France.
Plateforme Proteomique Strasbourg - Esplanade, Institut de Biologie Moléculaire et Cellulaire, CNRS FR1589, 15 rue Descartes, 67084 Strasbourg Cedex, France.
Mol Cell. 2019 Jun 20;74(6):1227-1238.e3. doi: 10.1016/j.molcel.2019.03.030. Epub 2019 Apr 16.
rRNAs and tRNAs universally require processing from longer primary transcripts to become functional for translation. Here, we describe an unsuspected link between tRNA maturation and the 3' processing of 16S rRNA, a key step in preparing the small ribosomal subunit for interaction with the Shine-Dalgarno sequence in prokaryotic translation initiation. We show that an accumulation of either 5' or 3' immature tRNAs triggers RelA-dependent production of the stringent response alarmone (p)ppGpp in the Gram-positive model organism Bacillus subtilis. The accumulation of (p)ppGpp and accompanying decrease in GTP levels specifically inhibit 16S rRNA 3' maturation. We suggest that cells can exploit this mechanism to sense potential slowdowns in tRNA maturation and adjust rRNA processing accordingly to maintain the appropriate functional balance between these two major components of the translation apparatus.
rRNAs 和 tRNAs 通常需要从较长的初级转录物中进行加工,才能成为翻译的功能。在这里,我们描述了 tRNA 成熟和 16S rRNA 3' 加工之间的一个意外联系,这是准备小核糖体亚基与原核翻译起始中的 Shine-Dalgarno 序列相互作用的关键步骤。我们表明,5' 或 3' 不成熟 tRNA 的积累会触发革兰氏阳性模式生物枯草芽孢杆菌中 RelA 依赖性产生严格反应信号分子(p)ppGpp。(p)ppGpp 的积累和伴随的 GTP 水平下降特异性抑制 16S rRNA 3' 成熟。我们认为,细胞可以利用这种机制来感知 tRNA 成熟的潜在减缓,并相应地调整 rRNA 加工,以维持翻译装置这两个主要组件之间的适当功能平衡。