Leslie David J, Heinen Christian, Schramm Frederic D, Thüring Marietta, Aakre Christopher D, Murray Sean M, Laub Michael T, Jonas Kristina
LOEWE Center for Synthetic Microbiology, Philipps University Marburg, Marburg, Germany; Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
LOEWE Center for Synthetic Microbiology, Philipps University Marburg, Marburg, Germany.
PLoS Genet. 2015 Jul 2;11(7):e1005342. doi: 10.1371/journal.pgen.1005342. eCollection 2015 Jul.
Bacteria can arrest their own growth and proliferation upon nutrient depletion and under various stressful conditions to ensure their survival. However, the molecular mechanisms responsible for suppressing growth and arresting the cell cycle under such conditions remain incompletely understood. Here, we identify post-transcriptional mechanisms that help enforce a cell-cycle arrest in Caulobacter crescentus following nutrient limitation and during entry into stationary phase by limiting the accumulation of DnaA, the conserved replication initiator protein. DnaA is rapidly degraded by the Lon protease following nutrient limitation. However, the rate of DnaA degradation is not significantly altered by changes in nutrient availability. Instead, we demonstrate that decreased nutrient availability downregulates dnaA translation by a mechanism involving the 5' untranslated leader region of the dnaA transcript; Lon-dependent proteolysis of DnaA then outpaces synthesis, leading to the elimination of DnaA and the arrest of DNA replication. Our results demonstrate how regulated translation and constitutive degradation provide cells a means of precisely and rapidly modulating the concentration of key regulatory proteins in response to environmental inputs.
细菌在营养物质耗尽以及处于各种应激条件下时,能够停止自身的生长和增殖,以确保其存活。然而,在这种情况下负责抑制生长和阻止细胞周期的分子机制仍未完全清楚。在这里,我们确定了转录后机制,该机制通过限制保守的复制起始蛋白DnaA的积累,在新月柄杆菌营养限制后和进入稳定期期间帮助实施细胞周期停滞。营养限制后,DnaA会被Lon蛋白酶迅速降解。然而,营养物质可用性的变化并不会显著改变DnaA的降解速率。相反,我们证明营养物质可用性的降低通过一种涉及dnaA转录本5'非翻译前导区的机制下调dnaA的翻译;然后,Lon依赖的DnaA蛋白水解作用超过了合成作用,导致DnaA的消除和DNA复制的停滞。我们的结果表明,受调控的翻译和组成型降解如何为细胞提供一种手段,以精确、快速地调节关键调节蛋白的浓度,以响应环境输入。