Hallier Marc, Ivanova Natalia, Rametti Armelle, Pavlov Michael, Ehrenberg Måns, Felden Brice
Biochimie Pharmaceutique, Universite de Rennes I, Unite Propre a la Recherche et a l'Enseignement Superieur Jeune Equipe 2311, 2 avenue du Pr. Leon Bernard, 35043 Rennes, France.
J Biol Chem. 2004 Jun 18;279(25):25978-85. doi: 10.1074/jbc.M314086200. Epub 2004 Apr 6.
To rescue stalled ribosomes, eubacteria employ a molecule, transfer messenger RNA (tmRNA), which functions both as a tRNA and as an mRNA. With the help of small protein B (SmpB), tmRNA restarts protein synthesis and adds by the trans-translation mechanism a peptide tag to the stalled protein to target it for destruction by cellular proteases. Here, the cellular location and expression of endogenous SmpB were monitored in vivo. We report that SmpB is associated with 70S ribosomes and not in the soluble fraction, independently of the presence of tmRNA. In vitro, SmpB that is pre-bound to a stalled ribosome can trigger initiation of trans-translation. Our results demonstrate the existence of a novel pathway for the entry of tmRNA to the ribosome and for the trans-transfer of a nascent peptide chain from peptidyl-tRNA to charged tmRNA.
为了拯救停滞的核糖体,真细菌利用一种名为转移信使核糖核酸(tmRNA)的分子,它兼具转运核糖核酸(tRNA)和信使核糖核酸(mRNA)的功能。在小蛋白B(SmpB)的帮助下,tmRNA重新启动蛋白质合成,并通过反式翻译机制给停滞的蛋白质添加一个肽标签,使其被细胞蛋白酶降解。在此,我们在体内监测了内源性SmpB的细胞定位和表达。我们报告称,SmpB与70S核糖体相关联,而非存在于可溶性组分中,这与tmRNA的存在无关。在体外,预先结合到停滞核糖体上的SmpB能够触发反式翻译的起始。我们的结果证明了存在一条新的途径,可使tmRNA进入核糖体,并使新生肽链从肽基-tRNA反式转移至带电的tmRNA。