Collier Justine, Binet Emmanuelle, Bouloc Philippe
Laboratoire des Réseaux de Régulations, Institut de Génétique et Microbiologie, Université Paris-Sud, CNRS/UMR 8621, Orsay, France.
Mol Microbiol. 2002 Aug;45(3):745-54. doi: 10.1046/j.1365-2958.2002.03045.x.
SsrA is a tmRNA involved in tagging polypeptides on stalled ribosomes. The resulting fusion proteins are then degraded. We purified endogenous SsrA-tagged proteins by means of a genetically engineered SsrA and identified some of them. Analysis of the proteins suggested that they are tagged at their C-terminal extremities. One of them, ribokinase, is expressed from a messenger with a poorly efficient stop codon, leading to translational recoding events. A change in the ribokinase coding sequence from a weak to a strong translational stop sequence (UGAc to UAAu) annihilated SsrA tagging. Translational termination by UGA recruits the translational release factor (RF) 2. We observed that SsrA tagging of ribokinase was inversely correlated with RF2 activity, revealing a dynamic competition between translational termination and SsrA tagging.
SsrA是一种参与在停滞核糖体上标记多肽的反式翻译信使核糖核酸(tmRNA)。由此产生的融合蛋白随后被降解。我们通过基因工程改造的SsrA纯化了内源性SsrA标记的蛋白质,并鉴定出其中一些。对这些蛋白质的分析表明,它们在其C末端被标记。其中之一,核糖激酶,由一个具有低效终止密码子的信使核糖核酸表达,导致翻译重编码事件。核糖激酶编码序列从弱翻译终止序列(UGAc)变为强翻译终止序列(UAAu)消除了SsrA标记。UGA介导的翻译终止招募翻译释放因子(RF)2。我们观察到核糖激酶的SsrA标记与RF2活性呈负相关,揭示了翻译终止和SsrA标记之间的动态竞争。