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Transcriptional and translational regulation in Arc protein network of Escherichia coli's stress response (1609.09202v1)

Published 29 Sep 2016 in q-bio.MN

Abstract: Recently, there has been a lot of effort in understanding sRNA mediated regulation of gene expression and how this mode of regulation differs from transcriptional regulation.In E.coli, in the presence of oxidative stress, the synthesis of sigmas is regulated through an interesting mechanism involving both transcriptional and sRNA-mediated translational regulation. The key regulatory factors involved in transcriptional and translational regulation are ArcA and ArcB proteins and ArcZ sRNA, respectively. Phosphorylated ArcA, in a feedforward mechanism, represses the transcriptions sigmas and ArcZ sRNA with the latter being a post-transcriptional activator for sigmas. Through a feedback mechanisms, ArcZ sRNA destabilises ArcB mRNA and regulates the level of ArcB protein, a kinase that phosphorylates ArcA. The oxygen and energy availability is expected to influence the ArcA phosphorylation rate and, as a consequence, in equilibrium, the system is likely to be in either a high ArcB (low ArcZ) or a low ArcB (high ArcZ) state. Kinetic modelling studies suggest that the rate of destabilisation of ArcB mRNA by ArcZ sRNA must be appropriately tuned for achieving the desired state. In particular, for a high phosphorylation rate, the transition from a low to a high ArcZ synthesis regime with the increase in sRNA-mRNA interaction is similar to the threshold-linear response observed earlier. Further, we show that the mRNA destabilisation by sRNA might be, in particular, beneficial in the low phosphorylation state for having the right concentration levels of ArcZ and ArcB. Stochastic simulation results suggest that as the ArcZ-ArcB binding affinity is increased, the probability distribution for the number of ArcZ molecules becomes flatter indicating frequently occurring transcriptional bursts of varying strengths.

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