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Spatial organization of bacterial transcription and translation

Author(s): Castellana, Michele; Hsin-Jung Li, Sophia; Wingreen, Ned

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dc.contributor.authorCastellana, Michele-
dc.contributor.authorHsin-Jung Li, Sophia-
dc.contributor.authorWingreen, Ned-
dc.identifier.citationCastellana, Michele, Hsin-Jung Li, Sophia, Wingreen, Ned S. (2016). Spatial organization of bacterial transcription and translation. Proceedings of the National Academy of Sciences, 113 (33), 9286 - 9291. doi:10.1073/pnas.1604995113en_US
dc.description.abstractIn bacteria such as Escherichia coli, DNA is compacted into a nucleoid near the cell center, while ribosomes—molecular complexes that translate messenger RNAs (mRNAs) into proteins—are mainly localized to the poles. We study the impact of this spatial organization using a minimal reaction-diffusion model for the cellular transcriptional-translational machinery. While genome-wide mRNA-nucleoid segregation still lacks experimental validation, our model predicts that ∼ 90% of mRNAs are segregated to the poles. In addition, our analysis reveals a “circulation” of ribosomes driven by the flux of mRNAs, from synthesis in the nucleoid to degradation at the poles. We show that our results are robust with respect to multiple, biologically relevant factors, such as mRNA degradation by RNase enzymes, different phases of the cell division cycle and growth rates, and the existence of non-specific, transient interactions between ribosomes and mRNAs. Finally, we confirm that the observed nucleoid size stems from a balance between the forces that the chromosome and mRNAs exert on each other. This suggests a potential global feedback circuit in which gene expression feeds back on itself via nucleoid compaction.en_US
dc.format.extent9286 - 9291en_US
dc.relation.ispartofProceedings of the National Academy of Sciencesen_US
dc.rightsAuthor's manuscripten_US
dc.titleSpatial organization of bacterial transcription and translationen_US
dc.typeJournal Articleen_US

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